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| {{DrugProjectFormSinglePage
| | #REDIRECT [[Aprepitant]] |
| |authorTag={{AP}}
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| |genericName=Aprepitant
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| |aOrAn=an
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| |drugClass=[[antiemetic]], [[neurokinin-1 receptor antagonist]]
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| |indicationType=prophylaxis
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| |indication=in combination with other antiemetic agents for the:
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| *acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy (HEC) including high-dose cisplatin
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| *of [[nausea]] and [[vomiting]] associated with initial and repeat courses of moderately emetogenic cancer [[chemotherapy]] (MEC)
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| Also, indicated for the prevention of postoperative nausea and vomiting (PONV)
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| |adverseReactions=[[alopecia]], [[anorexia]], [[asthenia]]/[[fatigue]], [[constipation]], [[diarrhea]], [[headache]], [[hiccups]], [[nausea]], [[hypotension]], [[pruritus]], [[pyrexia]]
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| |blackBoxWarningTitle=<b><span style="color:#FF0000;">TITLE</span></b>
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| |blackBoxWarningBody=<i><span style="color:#FF0000;">Condition Name:</span></i> (Content)
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| |fdaLIADAdult======Prevention of Chemotherapy Induced Nausea and Vomiting (CINV)=====
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| Capsules of Aprepitant (aprepitant) are given for 3 days as part of a regimen that includes a corticosteroid and a 5-HT3 antagonist. The recommended dose of Aprepitant is 125 mg orally 1 hour prior to chemotherapy treatment (Day 1) and 80 mg orally once daily in the morning on Days 2 and 3.
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| *Aprepitant may be taken with or without food.
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| *Aprepitant (fosaprepitant dimeglumine) for Injection (115 mg) is a prodrug of aprepitant and may be substituted for oral Aprepitant (125 mg), 30 minutes prior to chemotherapy, on Day 1 only of the CINV regimen as an intravenous infusion administered over 15 minutes.
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| In clinical studies with Aprepitant, the following regimen was used for the prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy:
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| [[file:Aprepitant Dosage1.png|none|300px]]
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| In a clinical study with Aprepitant, the following regimen was used for the prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy:
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| [[file:Aprepitant Dosage2.png|none|300px]]
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| =====Prevention of Postoperative Nausea and Vomiting (PONV)=====
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| The recommended oral dosage of Aprepitant is 40 mg within 3 hours prior to induction of anesthesia. Aprepitant may be taken with or without food.
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| |offLabelAdultGuideSupport=There is limited information regarding <i>Off-Label Guideline-Supported Use</i> of Aprepitant (patient information) in adult patients.
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| |offLabelAdultNoGuideSupport=There is limited information regarding <i>Off-Label Non–Guideline-Supported Use</i> of Aprepitant (patient information) in adult patients.
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| |offLabelPedGuideSupport=There is limited information regarding <i>Off-Label Guideline-Supported Use</i> of Aprepitant (patient information) in pediatric patients.
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| |offLabelPedNoGuideSupport=There is limited information regarding <i>Off-Label Non–Guideline-Supported Use</i> of Aprepitant (patient information) in pediatric patients.
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| |contraindications=Aprepitant is contraindicated in patients who are [[hypersensitive]] to any component of the product. Aprepitant is a dose-dependent inhibitor of [[cytochrome P450]] isoenzyme 3A4 ([[CYP3A4]]). Aprepitant should not be used concurrently with [[pimozide]], [[terfenadine]], [[astemizole]], or [[cisapride]]. Inhibition of [[CYP3A4]] by [[aprepitant]] could result in elevated plasma concentrations of these drugs, potentially causing serious or life-threatening reactions.
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| |warnings======CYP3A4 Interactions=====
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| *Aprepitant (aprepitant), a dose-dependent inhibitor of [[CYP3A4]], should be used with caution in patients receiving concomitant medications that are primarily metabolized through [[CYP3A4]]. Moderate inhibition of [[CYP3A4]] by aprepitant, 125 mg/80 mg regimen, could result in elevated plasma concentrations of these concomitant medications.
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| *Weak inhibition of [[CYP3A4]] by a single 40 mg dose of aprepitant is not expected to alter the plasma concentrations of concomitant medications that are primarily metabolized through [[CYP3A4]] to a clinically significant degree.
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| *When aprepitant is used concomitantly with another [[CYP3A4]] inhibitor, aprepitant plasma concentrations could be elevated. When Aprepitant is used concomitantly with medications that induce [[CYP3A4]] activity aprepitant plasma concentrations could be reduced and this may result in decreased efficacy of Aprepitant.
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| *Chemotherapy agents that are known to be metabolized by [[CYP3A4]] include [[docetaxel]], [[paclitaxel]], [[etoposide]], [[irinotecan]], [[ifosfamide]], [[imatinib]], [[vinorelbine]], [[vinblastine]] and [[vincristine]]. In clinical studies, Aprepitant (125 mg/80 mg regimen) was administered commonly with [[etoposide]], [[vinorelbine]], or [[paclitaxel]]. The doses of these agents were not adjusted to account for potential drug interactions.
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| *In separate pharmacokinetic studies no clinically significant change in [[docetaxel]] or [[vinorelbine]] pharmacokinetics was observed when Aprepitant (125 mg/80 mg regimen) was co-administered.
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| *Due to the small number of patients in clinical studies who received the [[CYP3A4]] substrates [[vinblastine]], [[vincristine]], or [[ifosfamide]], particular caution and careful monitoring are advised in patients receiving these agents or other chemotherapy agents metabolized primarily by [[CYP3A4]] that were not studied.
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| =====Coadministration with Warfarin (a CYP2C9 substrate)=====
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| Coadministration of Aprepitant with [[warfarin]] may result in a clinically significant decrease in [[International Normalized Ratio]] ([[INR]]) of [[prothrombin time]]. In patients on chronic [[warfarin]] therapy, the [[INR]] should be closely monitored in the 2-week period, particularly at 7 to 10 days, following initiation of the 3-day regimen of Aprepitant with each chemotherapy cycle, or following administration of a single 40 mg dose of Aprepitant for the prevention of postoperative [[nausea]] and [[vomiting]].
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| =====Coadministration with Hormonal Contraceptives=====
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| Upon coadministration with Aprepitant, the efficacy of [[hormonal contraceptives]] during and for 28 days following the last dose of Aprepitant may be reduced. Alternative or back-up methods of contraception should be used during treatment with Aprepitant and for 1 month following the last dose of Aprepitant.
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| =====Patients with Severe Hepatic Impairment=====
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| There are no clinical or pharmacokinetic data in patients with severe hepatic [[impairment]] ([Child-Pugh score]] >9). Therefore, caution should be exercised when Aprepitant is administered in these patients.
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| =====Chronic Continuous Use=====
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| Chronic continuous use of Aprepitant for prevention of [[nausea]] and [[vomiting]] is not recommended because it has not been studied; and because the drug interaction profile may change during chronic continuous use.
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| |clinicalTrials=In 2 well-controlled clinical trials in patients receiving highly emetogenic cancer chemotherapy, 544 patients were treated with aprepitant during Cycle 1 of chemotherapy and 413 of these patients continued into the Multiple-Cycle extension for up to 6 cycles of chemotherapy. Aprepitant was given in combination with ondansetron and dexamethasone.
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| In Cycle 1, clinical adverse experiences were reported in approximately 69% of patients treated with the aprepitant regimen compared with approximately 68% of patients treated with standard therapy. Table 1 shows the percent of patients with clinical adverse experiences reported at an incidence ≥3%.
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| [[file:Aprepitant AR1.png|none|400px]]
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| In a combined analysis of these two studies, isolated cases of serious adverse experiences were similar in the two treatment groups.
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| Highly and Moderately Emetogenic Chemotherapy
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| The following additional clinical adverse experiences (incidence >0.5% and greater than standard therapy), regardless of causality, were reported in patients treated with aprepitant regimen in either HEC or MEC studies:
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| *Infections and infestations: [[candidiasis]], [[herpes simplex]], lower respiratory infection, [[oral candidiasis]], [[pharyngitis]], [[septic shock]], upper respiratory infection, [[urinary tract infection]].
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| *Neoplasms benign, malignant and unspecified (including cysts and polyps): [[malignant neoplasm]], [[non-small cell lung carcinoma]].
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| *Blood and lymphatic system disorders: [[anemia]], [[febrile neutropenia]], [[thrombocytopenia]].
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| *Metabolism and nutrition disorders: [[appetite decreased]], [[diabetes mellitus]], [[hypokalemia]].
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| *Psychiatric disorders: [[anxiety disorder]], [[confusion]], [[depression]].
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| *Nervous system: [[peripheral neuropathy]], [[sensory neuropathy]], [[taste disturbance]], [[tremor]].
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| *Eye disorders: [[conjunctivitis]].
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| *Cardiac disorders: [[myocardial infarction]], [[palpitations]], [[tachycardia]].
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| *Vascular disorders: [[deep venous thrombosis]], [[flushing]], [[hot flush]], [[hypertension]], [[hypotension]].
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| *Respiratory, thoracic and mediastinal disorders: [[cough]], [[dyspnea]], [[nasal secretion]], [[pharyngolaryngeal pain]], [[pneumonitis]], [[pulmonary embolism]], [[respiratory insufficiency]], [[vocal disturbance]].
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| *Gastrointestinal disorders: [[abdominal pain upper]], [[acid reflux]], [[deglutition disorder]], [[dry mouth]], [[dysgeusia]], [[dysphagia]], [[eructation]], [[flatulence]], [[obstipation]], [[salivation increased]].
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| *Skin and subcutaneous tissue disorders: [[acne]], [[diaphoresis]], [[pruritus]], [[rash]].
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| *Musculoskeletal and connective tissue disorders: [[arthralgia]], [[back pain]], [[muscular weakness]], [[musculoskeletal pain]], [[myalgia]].
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| *Renal and urinary disorders: [[dysuria]], [[renal insufficiency]].
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| *Reproductive system and breast disorders: [[pelvic pain]].
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| *General disorders and administrative site conditions: [[edema]], [[malaise]], [[pain]], [[rigors]].
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| *Investigations: [[weight loss]].
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| *Stevens-Johnson syndrome was reported as a serious adverse experience in a patient receiving aprepitant with cancer chemotherapy in another CINV study.
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| Laboratory Adverse Experiences
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| Table 3 shows the percent of patients with laboratory adverse experiences reported at an incidence ≥3% in patients receiving highly emetogenic chemotherapy.
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| [[file:Aprepitant AR2.png|none|400px]]
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| The following additional laboratory adverse experiences (incidence >0.5% and greater than standard therapy), regardless of causality, were reported in patients treated with aprepitant regimen: [[alkaline phosphatase]] increased, [[hyperglycemia]], [[hyponatremia]], [[leukocytes]] increased, [[erythrocyturia]], [[leukocyturia]].
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| The adverse experience profiles in the Multiple-Cycle extensions of HEC and MEC studies for up to 6 cycles of chemotherapy were generally similar to that observed in Cycle 1.
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| ======Postoperative Nausea and Vomiting======
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| In well-controlled clinical studies in patients receiving general anesthesia, 564 patients were administered 40 mg aprepitant orally and 538 patients were administered 4 mg ondansetron IV.
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| Clinical adverse experiences were reported in approximately 60% of patients treated with 40 mg aprepitant compared with approximately 64% of patients treated with 4 mg ondansetron IV. Table 4 shows the percent of patients with clinical adverse experiences reported at an incidence ≥3% of the combined studies.
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| [[file:Aprepitant AR3.png||none|400px]]
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| The following additional clinical adverse experiences (incidence >0.5% and greater than ondansetron), regardless of causality, were reported in patients treated with aprepitant:
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| *Infections and infestations: [[postoperative infection]]
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| *Metabolism and nutrition disorders: [[hypokalemia]], [[hypovolemia]].
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| *Nervous system disorders: [[dizziness]], [[hypoesthesia]], [[syncope]].
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| *Vascular disorders: [[hematoma]]
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| *Respiratory, thoracic and mediastinal disorders: [[dyspnea]], [[hypoxia]], [[respiratory depression]].
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| *Gastrointestinal disorders: [[abdominal pain]], [[abdominal pain upper]], [[dry mouth]], [[dyspepsia]].
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| *Skin and subcutaneous tissue disorders: [[urticaria]]
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| *General disorders and administrative site conditions: [[hypothermia]], [[pain]].
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| *Investigations: [[hypotension]]
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| Injury, poisoning and procedural complications: [[operative hemorrhage]], wound dehiscence.
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| Other adverse experiences (incidence ≤0.5%) reported in patients treated with aprepitant 40 mg for postoperative nausea and vomiting included:
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| *Nervous system disorders: [[dysarthria]], [[sensory disturbance]].
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| *Eye disorders: [[miosis]], [[visual acuity reduced]].
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| *Respiratory, thoracic and mediastinal disorders: [[wheezing]]
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| *Gastrointestinal disorders: bowel sounds abnormal, stomach discomfort.
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| There were no serious adverse drug-related experiences reported in the postoperative nausea and vomiting clinical studies in patients taking 40 mg aprepitant.
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| Laboratory Adverse Experiences
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| One laboratory adverse experience, hemoglobin decreased (40 mg aprepitant 3.8%, ondansetron 4.2%), was reported at an incidence ≥3% in a patient receiving general anesthesia.
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| The following additional laboratory adverse experiences (incidence >0.5% and greater than ondansetron), regardless of causality, were reported in patients treated with aprepitant 40 mg: blood albumin decreased, blood bilirubin increased, blood glucose increased, blood potassium decreased, glucose urine present.
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| The adverse experience of ALT increased occurred with similar incidence in patients treated with aprepitant 40 mg (1.1%) as in patients treated with ondansetron 4 mg (1.0%).
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| Other Studies
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| In addition, two serious adverse experiences were reported in postoperative nausea and vomiting (PONV) clinical studies in patients taking a higher dose of aprepitant: one case of constipation, and one case of sub-ileus.
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| Angioedema and urticaria were reported as serious adverse experiences in a patient receiving aprepitant in a non-CINV/non-PONV study.
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| |postmarketing=The following adverse reactions have been identified during postmarketing use of aprepitant. Because these reactions are reported voluntarily from a population of uncertain size, it is generally not possible to reliably estimate their frequency or establish a causal relationship to the drug.
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| Skin and subcutaneous tissue disorders: pruritus, rash, urticaria.
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| Immune system disorders: hypersensitivity reactions including anaphylactic reactions.
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| |drugInteractions======Effect of Aprepitant on the Pharmacokinetics of Other Agents=====
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| ======CYP3A4 Substrates======
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| *Weak inhibition of [[CYP3A4]] by a single 40 mg dose of aprepitant is not expected to alter the plasma concentrations of concomitant medications that are primarily metabolized through CYP3A4 to a clinically significant degree. However, higher aprepitant doses or repeated dosing at any aprepitant dose may have a clinically significant effect.
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| *As a moderate inhibitor of CYP3A4 at a dose of 125 mg/80 mg, aprepitant can increase plasma concentrations of concomitantly administered oral medications that are metabolized through CYP3A4. The use of [[fosaprepitant]] may increase [[CYP3A4]] substrate plasma concentrations to a lesser degree than the use of oral aprepitant (125 mg).
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| ======5-HT3 antagonists======
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| In clinical drug interaction studies, aprepitant did not have clinically important effects on the pharmacokinetics of [[ondansetron]], [[granisetron]], or [[hydrodolasetron]] (the active metabolite of [[dolasetron]]).
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| ======Corticosteroids======
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| *[[Dexamethasone]]: Aprepitant, when given as a regimen of 125 mg with [[dexamethasone]] coadministered orally as 20 mg on Day 1, and Aprepitant when given as 80 mg/day with [[dexamethasone]] coadministered orally as 8 mg on Days 2 through 5, increased the AUC of [[dexamethasone]], a CYP3A4 substrate, by 2.2-fold on Days 1 and 5. The oral [[dexamethasone]] doses should be reduced by approximately 50% when coadministered with Aprepitant (125 mg/80 mg regimen), to achieve exposures of [[dexamethasone]] similar to those obtained when it is given without Aprepitant. The daily dose of [[dexamethasone]] administered in clinical chemotherapy induced [[nausea]] and [[vomiting]] studies with Aprepitant reflects an approximate 50% reduction of the dose of [[dexamethasone]]. A single dose of Aprepitant (40 mg) when coadministered with a single oral dose of [[dexamethasone]] 20 mg, increased the AUC of [[dexamethasone]] by 1.45-fold. Therefore, no dose adjustment is recommended.
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| *[[Methylprednisolone]]: Aprepitant, when given as a regimen of 125 mg on Day 1 and 80 mg/day on Days 2 and 3, increased the AUC of [[methylprednisolone]], a [[CYP3A4]] substrate, by 1.34-fold on Day 1 and by 2.5-fold on Day 3, when [[methylprednisolone]] was coadministered intravenously as 125 mg on Day 1 and orally as 40 mg on Days 2 and 3. The IV [[methylprednisolone]] dose should be reduced by approximately 25%, and the oral [[methylprednisolone]] dose should be reduced by approximately 50% when coadministered with Aprepitant (125 mg/80 mg regimen) to achieve exposures of [[methylprednisolone]] similar to those obtained when it is given without Aprepitant Although the concomitant administration of [[methylprednisolone]] with the single 40 mg dose of aprepitant has not been studied, a single 40 mg dose of Aprepitant produces a weak inhibition of [[CYP3A4]] (based on [[midazolam]] interaction study) and it is not expected to alter the plasma concentrations of [[methylprednisolone]] to a clinically significant degree. Therefore, no dose adjustment is recommended.
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| ======Chemotherapeutic agents======
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| *[[Docetaxel]]: In a pharmacokinetic study, Aprepitant (125 mg/80 mg regimen) did not influence the pharmacokinetics of [[docetaxel]].
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| *[[Vinorelbine]]: In a pharmacokinetic study, Aprepitant (125 mg/80 mg regimen) did not influence the pharmacokinetics of [[vinorelbine]] to a clinically significant degree.
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| =====CYP2C9 Substrates (Warfarin, Tolbutamide)=====
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| Aprepitant has been shown to induce the metabolism of S(-) [[warfarin]] and [[tolbutamide]], which are metabolized through CYP2C9. Coadministration of Aprepitant with these drugs or other drugs that are known to be metabolized by [[CYP2C9]], such as [[phenytoin]], may result in lower plasma concentrations of these drugs.
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| ======Warfarin======
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| A single 125-mg dose of Aprepitant was administered on Day 1 and 80 mg/day on Days 2 and 3 to healthy subjects who were stabilized on chronic warfarin therapy. Although there was no effect of Aprepitant on the plasma AUC of R(+) or S(-) warfarin determined on Day 3, there was a 34% decrease in S(-) [[warfarin]] (a [[CYP2C9]] substrate) trough concentration accompanied by a 14% decrease in the prothrombin time (reported as International [[Normalized Ratio]] or [[INR]]) 5 days after completion of dosing with Aprepitant In patients on chronic [[warfarin]] therapy, the [[prothrombin time]] ([[INR]]) should be closely monitored in the 2-week period, particularly at 7 to 10 days, following initiation of the 3-day regimen of Aprepitant with each chemotherapy cycle, or following administration of a single 40 mg dose of Aprepitant for the prevention of postoperative [[nausea]] and [[vomiting]].
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| ======Tolbutamide======
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| *Aprepitant, when given as 125 mg on Day 1 and 80 mg/day on Days 2 and 3, decreased the AUC of [[tolbutamide]] (a [[CYP2C9]] substrate) by 23% on Day 4, 28% on Day 8, and 15% on Day 15, when a single dose of [[tolbutamide]] 500 mg was administered orally prior to the administration of the 3-day regimen of Aprepitant and on Days 4, 8, and 15.
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| *Aprepitant, when given as a 40-mg single oral dose on Day 1, decreased the AUC of [[tolbutamide]] (a CYP2C9 substrate) by 8% on Day 2, 16% on Day 4, 15% on Day 8, and 10% on Day 15, when a single dose of tolbutamide 500 mg was administered orally prior to the administration of Aprepitant 40 mg and on Days 2, 4, 8, and 15. This effect was not considered clinically important.
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| ======Oral contraceptives======
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| Aprepitant, when given once daily for 14 days as a 100-mg capsule with an oral contraceptive containing 35 mcg of [[ethinyl estradiol]] and 1 mg of [[norethindrone]], decreased the AUC of [[ethinyl estradiol]] by 43%, and decreased the AUC of [[norethindrone]] by 8%.
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| In another study, a daily dose of an oral contraceptive containing [[ethinyl estradiol]] and [[norethindrone]] was administered on Days 1 through 21, and Aprepitant was given as a 3-day regimen of 125 mg on Day 8 and 80 mg/day on Days 9 and 10 with [[ondansetron]] 32 mg IV on Day 8 and oral [[dexamethasone]] given as 12 mg on Day 8 and 8 mg/day on Days 9, 10, and 11. In the study, the AUC of [[ethinyl estradiol]] decreased by 19% on Day 10 and there was as much as a 64% decrease in ethinyl [[estradiol]] trough concentrations during Days 9 through 21. While there was no effect of Aprepitant on the AUC of [[norethindrone]] on Day 10, there was as much as a 60% decrease in [[norethindrone]] trough concentrations during Days 9 through 21.
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| In another study, a daily dose of an [[oral contraceptive]] containing [[ethinyl estradiol]] and [[norgestimate]] (which is converted to [[norelgestromin]]) was administered on Days 1 through 21, and Aprepitant 40 mg was given on Day 8. In the study, the AUC of [[ethinyl estradiol]] decreased by 4% and 29% on Day 8 and Day 12, respectively, while the AUC of [[norelgestromin]] increased by 18% on Day 8 and decreased by 10% on Day 12. In addition, the trough concentrations of [[ethinyl estradiol]] and [[norelgestromin]] on Days 8 through 21 were generally lower following coadministration of the oral contraceptive with Aprepitant 40 mg on Day 8 compared to the trough levels following administration of the [[oral contraceptive]] alone.
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| The coadministration of Aprepitant may reduce the efficacy of hormonal contraceptives (these can include birth control pills, skin patches, implants, and certain IUDs) during and for 28 days after administration of the last dose of Aprepitant. Alternative or back-up methods of contraception should be used during treatment with Aprepitant and for 1 month following the last dose of Aprepitant.
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| ======Midazolam======
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| Aprepitant increased the AUC of [[midazolam]], a sensitive [[CYP3A4]] substrate, by 2.3-fold on Day 1 and 3.3-fold on Day 5, when a single oral dose of [[midazolam]] 2 mg was coadministered on Day 1 and Day 5 of a regimen of Aprepitant 125 mg on Day 1 and 80 mg/day on Days 2 through 5. The potential effects of increased plasma concentrations of [[midazolam]] or other [[benzodiazepines]] metabolized via [[CYP3A4]] ([[alprazolam]], [[triazolam]]) should be considered when coadministering these agents with Aprepitant (125 mg/80 mg). A single dose of Aprepitant (40 mg) increased the AUC of midazolam by 1.2-fold on Day 1, when a single oral dose of [[midazolam]] 2 mg was coadministered on Day 1 with Aprepitant 40 mg; this effect was not considered clinically important.
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| In another study with intravenous administration of [[midazolam]], Aprepitant was given as 125 mg on Day 1 and 80 mg/day on Days 2 and 3, and [[midazolam]] 2 mg IV was given prior to the administration of the 3-day regimen of Aprepitant and on Days 4, 8, and 15. Aprepitant increased the AUC of [[midazolam]] by 25% on Day 4 and decreased the AUC of [[midazolam]] by 19% on Day 8 relative to the dosing of Aprepitant on Days 1 through 3. These effects were not considered clinically important. The AUC of [[midazolam]] on Day 15 was similar to that observed at baseline.
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| An additional study was completed with intravenous administration of midazolam and Aprepitant. Intravenous [[midazolam]] 2 mg was given 1 hour after oral administration of a single dose of Aprepitant 125 mg. The plasma AUC of [[midazolam]] was increased by 1.5-fold. Depending on clinical situations (e.g., elderly patients) and degree of monitoring available, dosage adjustment for intravenous midazolam may be necessary when it is coadministered with Aprepitant for the chemotherapy induced [[nausea]] and [[vomiting]] indication (125 mg on Day 1 followed by 80 mg on Days 2 and 3).
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| =====Effect of Other Agents on the Pharmacokinetics of Aprepitant=====
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| Aprepitant is a substrate for [[CYP3A4]]; therefore, coadministration of Aprepitant with drugs that inhibit [[CYP3A4]] activity may result in increased plasma concentrations of aprepitant. Consequently, concomitant administration of Aprepitant with strong [[CYP3A4 inhibitors]] (e.g., [[ketoconazole]], [[itraconazole]], [[nefazodone]], [[troleandomycin]], [[clarithromycin]], [[ritonavir]], [[nelfinavir]]) should be approached with caution. Because moderate [[CYP3A4 inhibitors]] (e.g., [[diltiazem]]) result in a 2-fold increase in plasma concentrations of aprepitant, concomitant administration should also be approached with caution.
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| Aprepitant is a substrate for CYP3A4; therefore, coadministration of Aprepitant with drugs that strongly induce [[CYP3A4]] activity (e.g., [[rifampin]], [[carbamazepine]], [[phenytoin]]) may result in reduced plasma concentrations of aprepitant that may result in decreased efficacy of Aprepitant.
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| ======Ketoconazole======
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| When a single 125-mg dose of Aprepitant was administered on Day 5 of a 10-day regimen of 400 mg/day of [[ketoconazole]], a strong [[CYP3A4 inhibitor]], the AUC of aprepitant increased approximately 5-fold and the mean terminal half-life of aprepitant increased approximately 3-fold. Concomitant administration of Aprepitant with strong [[CYP3A4 inhibitors]] should be approached cautiously.
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| ======Rifampin======
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| When a single 375-mg dose of Aprepitant was administered on Day 9 of a 14-day regimen of 600 mg/day of [[rifampin]], a strong [[CYP3A4]] inducer, the AUC of aprepitant decreased approximately 11-fold and the mean terminal half-life decreased approximately 3-fold. Coadministration of Aprepitant with drugs that induce [[CYP3A4]] activity may result in reduced plasma concentrations and decreased efficacy of Aprepitant.
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| =====Additional Interactions=====
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| Aprepitant is unlikely to interact with drugs that are substrates for the P-glycoprotein transporter, as demonstrated by the lack of interaction of Aprepitant with [[digoxin]] in a clinical drug interaction study.
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| *[[Diltiazem]]: In patients with mild to moderate hypertension, administration of aprepitant once daily, as a tablet formulation comparable to 230 mg of the capsule formulation, with diltiazem 120 mg 3 times daily for 5 days, resulted in a 2-fold increase of aprepitant AUC and a simultaneous 1.7-fold increase of diltiazem AUC. These pharmacokinetic effects did not result in clinically meaningful changes in ECG, heart rate or blood pressure beyond those changes induced by diltiazem alone.
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| *[[Paroxetine]]: Coadministration of once daily doses of aprepitant, as a tablet formulation comparable to 85 mg or 170 mg of the capsule formulation, with paroxetine 20 mg once daily, resulted in a decrease in AUC by approximately 25% and Cmax by approximately 20% of both aprepitant and paroxetine.
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| |FDAPregCat=B
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| |useInPregnancyFDA=Reproduction studies have been performed in rats at oral doses up to 1000 mg/kg twice daily (plasma AUC0‑24hr of 31.3 mcg•hr/mL, about 1.6 times the human exposure at the recommended dose) and in rabbits at oral doses up to 25 mg/kg/day (plasma AUC0‑24hr of 26.9 mcg•hr/mL, about 1.4 times the human exposure at the recommended dose) and have revealed no evidence of impaired fertility or harm to the fetus due to aprepitant. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.
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| |useInNursing=Aprepitant is excreted in the milk of rats. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for possible serious adverse reactions in nursing infants from aprepitant and because of the potential for tumorigenicity shown for aprepitant in rodent carcinogenicity studies, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.
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| |useInPed=Safety and effectiveness of Aprepitant in pediatric patients have not been established.
| |
| |useInGeri=In 2 well-controlled chemotherapy-induced nausea and vomiting clinical studies, of the total number of patients (N=544) treated with Aprepitant 31% were 65 and over, while 5% were 75 and over. In well-controlled postoperative nausea and vomiting clinical studies, of the total number of patients (N=1120) treated with Aprepitant 7% were 65 and over, while 2% were 75 and over. No overall differences in safety or effectiveness were observed between these subjects and younger subjects. Greater sensitivity of some older individuals cannot be ruled out. Dosage adjustment in the elderly is not necessary.
| |
| |useInRenalImpair=No dosage adjustment is necessary for patients with renal impairment or for patients with end stage renal disease (ESRD) undergoing hemodialysis.
| |
| |useInHepaticImpair=No dosage adjustment is necessary for patients with mild to moderate hepatic impairment (Child-Pugh score 5 to 9). There are no clinical data in patients with severe hepatic impairment (Child-Pugh score >9).
| |
| |overdose=No specific information is available on the treatment of overdosage.
| |
| Drowsiness and headache were reported in one patient who ingested 1440 mg of aprepitant. In the event of overdose, Aprepitant should be discontinued and general supportive treatment and monitoring should be provided. Because of the antiemetic activity of aprepitant, drug-induced emesis may not be effective. Aprepitant cannot be removed by hemodialysis.
| |
| |drugBox={{Drugbox2
| |
| | verifiedrevid = 457136600
| |
| | IUPAC_name = 5-([(2''R'',3''S'')-2-((''R'')-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy)-3-(4-fluorophenyl)morpholino]methyl)-1''H''-1,2,4-triazol-3(2''H'')-one
| |
| | image = Aprepitant Structure.png
| |
| | width = 200
| |
| | |
| <!--Clinical data-->
| |
| | tradename = Aprepitant
| |
| | Drugs.com = {{drugs.com|monograph|aprepitant-fosaprepitant-dimeglumine}}
| |
| | MedlinePlus = a604003
| |
| | pregnancy_AU = B1
| |
| | pregnancy_US = B
| |
| | legal_AU = S4
| |
| | legal_UK = POM
| |
| | legal_US = Rx-only
| |
| | routes_of_administration = Oral
| |
| | |
| <!--Pharmacokinetic data-->
| |
| | bioavailability = 60-65%
| |
| | protein_bound = >95%
| |
| | metabolism = [[Liver|Hepatic]] (mostly [[CYP3A4]]- mediated; some contributions by [[CYP2C19]] & [[CYP1A2]])
| |
| | elimination_half-life = 9-13 hours
| |
| | excretion = Urine (5%), faeces (86%)
| |
| | |
| <!--Identifiers-->
| |
| | CASNo_Ref = {{cascite|correct|CAS}}
| |
| | CAS_number_Ref = {{cascite|correct|??}}
| |
| | CAS_number = 170729-80-3
| |
| | ATC_prefix = A04
| |
| | ATC_suffix = AD12
| |
| | PubChem = 6918365
| |
| | DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| |
| | DrugBank = DB00673
| |
| | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| |
| | ChemSpiderID = 5293568
| |
| | UNII_Ref = {{fdacite|correct|FDA}}
| |
| | UNII = 1NF15YR6UY
| |
| | ChEBI_Ref = {{ebicite|correct|EBI}}
| |
| | ChEBI = 499361
| |
| | ChEMBL_Ref = {{ebicite|correct|EBI}}
| |
| | ChEMBL = 1471
| |
| | |
| <!--Chemical data-->
| |
| | C=23 | H=21 | F=7 | N=4 | O=3
| |
| | molecular_weight = 534.427 g/mol
| |
| | smiles = FC(F)(F)c1cc(cc(c1)C(F)(F)F)[C@H](O[C@H]4OCCN(CC/2=N/C(=O)NN\2)[C@H]4c3ccc(F)cc3)C
| |
| | InChI = 1/C23H21F7N4O3/c1-12(14-8-15(22(25,26)27)10-16(9-14)23(28,29)30)37-20-19(13-2-4-17(24)5-3-13)34(6-7-36-20)11-18-31-21(35)33-32-18/h2-5,8-10,12,19-20H,6-7,11H2,1H3,(H2,31,32,33,35)/t12-,19+,20-/m1/s1
| |
| | InChIKey = ATALOFNDEOCMKK-OITMNORJBX
| |
| | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| |
| | StdInChI = 1S/C23H21F7N4O3/c1-12(14-8-15(22(25,26)27)10-16(9-14)23(28,29)30)37-20-19(13-2-4-17(24)5-3-13)34(6-7-36-20)11-18-31-21(35)33-32-18/h2-5,8-10,12,19-20H,6-7,11H2,1H3,(H2,31,32,33,35)/t12-,19+,20-/m1/s1
| |
| | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| |
| | StdInChIKey = ATALOFNDEOCMKK-OITMNORJSA-N
| |
| }}
| |
| |mechAction=Aprepitant is a selective high-affinity antagonist of human substance P/neurokinin 1 (NK1) receptors. Aprepitant has little or no affinity for serotonin (5-HT3), dopamine, and corticosteroid receptors, the targets of existing therapies for chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea and vomiting (PONV).
| |
| | |
| Aprepitant has been shown in animal models to inhibit emesis induced by cytotoxic chemotherapeutic agents, such as cisplatin, via central actions. Animal and human Positron Emission Tomography (PET) studies with aprepitant have shown that it crosses the blood brain barrier and occupies brain NK1 receptors. Animal and human studies show that aprepitant augments the antiemetic activity of the 5-HT3-receptor antagonist ondansetron and the corticosteroid dexamethasone and inhibits both the acute and delayed phases of cisplatin-induced emesis.
| |
| |structure=Chemically described as 5-(2R,3S)-2-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3-(4-fluorophenyl)-4-morpholinyl]methyl]-1,2-dihydro-3H-1,2,4-triazol-3-one.
| |
| | |
| Its empirical formula is C23H21F7N4O3, and its structural formula is:
| |
| [[file:Aprepitant Structure.png|none|300px]]
| |
| |PD======NK1 Receptor Occupancy=====
| |
| In two single-blind, multiple-dose, randomized, and placebo control studies, healthy young men received oral aprepitant doses of 10 mg (N=2), 30 mg (N=3), 100 mg (N=3) or 300 mg (N=5) once daily for 14 days with 2 or 3 subjects on placebo. Both plasma aprepitant concentration and NK1 receptor occupancy in the corpus striatum by positron emission tomography were evaluated, at predose and 24 hours after the last dose. At aprepitant plasma concentrations of ~10 ng/mL and ~100 ng/mL, the NK1 receptor occupancies were ~50% and ~90%, respectively. The oral aprepitant regimen for CINV produces mean trough plasma aprepitant concentrations >500 ng/mL, which would be expected to, based on the fitted curve with the Hill equation, result in >95% brain NK1 receptor occupancy. However, the receptor occupancy for either CINV or PONV dosing regimen has not been determined. In addition, the relationship between NK1 receptor occupancy and the clinical efficacy of aprepitant has not been established.
| |
| | |
| =====Cardiac Electrophysiology=====
| |
| In a randomized, double-blind, positive-controlled, thorough QTc study, a single 200-mg dose of fosaprepitant had no effect on the QTc interval. QT prolongation with the oral dosing regimens for CINV and PONV are not expected.
| |
| |PK======Absorption=====
| |
| Following oral administration of a single 40 mg dose of Aprepitant in the fasted state, mean area under the plasma concentration-time curve (AUC0‑∞) was 7.8 mcg•hr/mL and mean peak plasma concentration (Cmax) was 0.7 mcg/mL, occurring at approximately 3 hours postdose (Tmax). The absolute bioavailability at the 40‑mg dose has not been determined.
| |
| | |
| Following oral administration of a single 125-mg dose of Aprepitant on Day 1 and 80 mg once daily on Days 2 and 3, the AUC0-24hr was approximately 19.6 mcg•hr/mL and 21.2 mcg•hr/mL on Day 1 and Day 3, respectively. The Cmax of 1.6 mcg/mL and 1.4 mcg/mL were reached in approximately 4 hours (Tmax) on Day 1 and Day 3, respectively. At the dose range of 80-125 mg, the mean absolute oral bioavailability of aprepitant is approximately 60 to 65%. Oral administration of the capsule with a standard high-fat breakfast had no clinically meaningful effect on the bioavailability of aprepitant.
| |
| | |
| The pharmacokinetics of aprepitant are non-linear across the clinical dose range. In healthy young adults, the increase in AUC0‑∞ was 26% greater than dose proportional between 80‑mg and 125‑mg single doses administered in the fed state.
| |
| | |
| =====Distribution=====
| |
| Aprepitant is greater than 95% bound to plasma proteins. The mean apparent volume of distribution at steady state (Vdss) is approximately 70 L in humans. Aprepitant crosses the [[placenta]] in rats and rabbits and crosses the [[blood brain barrier]] in humans.
| |
| | |
| =====Metabolism=====
| |
| Aprepitant undergoes extensive metabolism. In vitro studies using human liver microsomes indicate that aprepitant is metabolized primarily by CYP3A4 with minor metabolism by [[CYP1A2]] and [[CYP2C19]]. Metabolism is largely via oxidation at the [[morpholine]] ring and its side chains. No metabolism by [[CYP2D6]], [[CYP2C9]], or [[CYP2E1]] was detected. In healthy young adults, aprepitant accounts for approximately 24% of the radioactivity in plasma over 72 hours following a single oral 300-mg dose of [14C]-aprepitant, indicating a substantial presence of metabolites in the plasma. Seven metabolites of aprepitant, which are only weakly active, have been identified in human plasma.
| |
| | |
| =====Excretion=====
| |
| Following administration of a single IV 100-mg dose of [14C]-aprepitant prodrug to healthy subjects, 57% of the radioactivity was recovered in urine and 45% in feces. A study was not conducted with radiolabeled capsule formulation. The results after oral administration may differ.
| |
| | |
| Aprepitant is eliminated primarily by metabolism; aprepitant is not renally excreted. The apparent plasma clearance of aprepitant ranged from approximately 62 to 90 mL/min. The apparent terminal half-life ranged from approximately 9 to 13 hours. | |
| |nonClinToxic======Carcinogenesis, Mutagenesis, Impairment of Fertility=====
| |
| Carcinogenicity studies were conducted in Sprague-Dawley rats and in CD-1 mice for 2 years. In the rat carcinogenicity studies, animals were treated with oral doses ranging from 0.05 to 1000 mg/kg twice daily. The highest dose produced a systemic exposure to aprepitant (plasma AUC0‑24hr) of 0.7 to 1.6 times the human exposure (AUC0‑24hr = 19.6 mcg•hr/mL) at the recommended dose of 125 mg/day. Treatment with aprepitant at doses of 5 to 1000 mg/kg twice daily caused an increase in the incidences of [[thyroid follicular cell adenomas]] and [[thyroid carcinomas]] in male rats. In female rats, it produced [[hepatocellular adenomas]] at 5 to 1000 mg/kg twice daily and [[hepatocellular carcinomas]] and [[thyroid follicular cell adenomas]] at 125 to 1000 mg/kg twice daily. In the mouse carcinogenicity studies, the animals were treated with oral doses ranging from 2.5 to 2000 mg/kg/day. The highest dose produced a systemic exposure of about 2.8 to 3.6 times the human exposure at the recommended dose. Treatment with aprepitant produced [[skin fibrosarcomas]] at 125 and 500 mg/kg/day doses in male mice.
| |
| | |
| Aprepitant was not genotoxic in the [[Ames test]], the human lymphoblastoid cell ([[TK6]]) mutagenesis test, the rat hepatocyte DNA strand break test, the Chinese hamster ovary (CHO) cell chromosome aberration test and the mouse micronucleus test.
| |
| | |
| Aprepitant did not affect the fertility or general reproductive performance of male or female rats at doses up to the maximum feasible dose of 1000 mg/kg twice daily (providing exposure in male rats lower than the exposure at the recommended human dose and exposure in female rats at about 1.6 times the human exposure).
| |
| |clinicalStudies=====Prevention of Chemotherapy Induced Nausea and Vomiting (CINV)====
| |
| Oral administration of Aprepitant in combination with ondansetron and dexamethasone (aprepitant regimen) has been shown to prevent acute and delayed nausea and vomiting associated with highly emetogenic chemotherapy including high-dose cisplatin, and nausea and vomiting associated with moderately emetogenic chemotherapy.
| |
| | |
| =====Highly Emetogenic Chemotherapy (HEC)=====
| |
| In 2 multicenter, randomized, parallel, double-blind, controlled clinical studies, the aprepitant regimen (see Table 6) was compared with standard therapy in patients receiving a chemotherapy regimen that included [[cisplatin]] >50 mg/m2 (mean [[cisplatin]] dose = 80.2 mg/m2). Of the 550 patients who were randomized to receive the aprepitant regimen, 42% were women, 58% men, 59% White, 3% Asian, 5% Black, 12% Hispanic American, and 21% Multi-Racial. The aprepitant-treated patients in these clinical studies ranged from 14 to 84 years of age, with a mean age of 56 years. 170 patients were 65 years or older, with 29 patients being 75 years or older. Patients (N = 1105) were randomized to either the aprepitant regimen (N = 550) or standard therapy (N = 555). The treatment regimens are defined in Table 5.
| |
| | |
| [[file:Aprepitant CS1.png|none|350px]]
| |
| | |
| During these studies 95% of the patients in the aprepitant group received a concomitant chemotherapeutic agent in addition to protocol-mandated cisplatin. The most common chemotherapeutic agents and the number of aprepitant patients exposed follows: etoposide (106), fluorouracil (100), gemcitabine (89), vinorelbine (82), paclitaxel (52), cyclophosphamide (50), doxorubicin (38), docetaxel (11).
| |
| | |
| The antiemetic activity of Aprepitant was evaluated during the acute phase (0 to 24 hours post-cisplatin treatment), the delayed phase (25 to 120 hours post-cisplatin treatment) and overall (0 to 120 hours post-cisplatin treatment) in Cycle 1. Efficacy was based on evaluation of the following endpoints:
| |
| | |
| Primary endpoint:
| |
| *complete response (defined as no emetic episodes and no use of rescue therapy)
| |
| | |
| Other prespecified endpoints:
| |
| *complete protection (defined as no [[emetic episodes]], no use of rescue therapy, and a maximum [[nausea]] visual analogue scale [[[VAS]]] score <25 mm on a 0 to 100 mm scale)
| |
| *no [[emesis]] (defined as no emetic episodes regardless of use of rescue therapy)
| |
| *no [[nausea]] (maximum [[VAS]] <5 mm on a 0 to 100 mm scale)
| |
| *no significant [[nausea]] (maximum [[VAS]] <25 mm on a 0 to 100 mm scale)
| |
| | |
| [[file:Aprepitant CS2.png|none|400px]]
| |
| | |
| [[file:Aprecitant CS3.png|none|400px]]
| |
| | |
| In both studies, a statistically significantly higher proportion of patients receiving the aprepitant regimen in Cycle 1 had a complete response in the overall phase (primary endpoint), compared with patients receiving standard therapy. A statistically significant difference in complete response in favor of the aprepitant regimen was also observed when the acute phase and the delayed phase were analyzed separately.
| |
| | |
| In both studies, the estimated time to first emesis after initiation of cisplatin treatment was longer with the aprepitant regimen, and the incidence of first emesis was reduced in the aprepitant regimen group compared with standard therapy group as depicted in the Kaplan-Meier curves in Figure 1.
| |
| | |
| [[file:Aprepitant CS4.png|none|400px]]
| |
| | |
| *Patient-Reported Outcomes: The impact of nausea and vomiting on patients’ daily lives was assessed in Cycle 1 of both Phase III studies using the Functional Living Index–Emesis (FLIE), a validated nausea- and vomiting-specific patient-reported outcome measure. Minimal or no impact of nausea and vomiting on patients’ daily lives is defined as a FLIE total score >108. In each of the 2 studies, a higher proportion of patients receiving the aprepitant regimen reported minimal or no impact of nausea and vomiting on daily life (Study 1: 74% versus 64%; Study 2: 75% versus 64%).
| |
| | |
| *Multiple-Cycle Extension: In the same 2 clinical studies, patients continued into the Multiple-Cycle extension for up to 5 additional cycles of chemotherapy. The proportion of patients with no emesis and no significant nausea by treatment group at each cycle is depicted in Figure 2. Antiemetic effectiveness for the patients receiving the aprepitant regimen is maintained throughout repeat
| |
| | |
| =====Moderately Emetogenic Chemotherapy (MEC)=====
| |
| In a multicenter, randomized, double-blind, parallel-group, clinical study in breast cancer patients, the aprepitant regimen (see Table 9) was compared with a standard of care therapy in patients receiving a moderately emetogenic chemotherapy regimen that included cyclophosphamide 750-1500 mg/m2; or cyclophosphamide 500-1500 mg/m2 and doxorubicin (≤60 mg/m2) or epirubicin (≤100 mg/m2). In this study, the most common combinations were cyclophosphamide + doxorubicin (60.6%); and cyclophosphamide + epirubicin + fluorouracil (21.6%). Of the 438 patients who were randomized to receive the aprepitant regimen, 99.5% were women. Of these, approximately 80% were White, 8% Black, 8% Asian, 4% Hispanic, and <1% Other. The aprepitant-treated patients in this clinical study ranged from 25 to 78 years of age, with a mean age of 53 years; 70 patients were 65 years or older, with 12 patients being over 74 years. Patients (N = 866) were randomized to either the aprepitant regimen (N = 438) or standard therapy (N = 428). The treatment regimens are defined in Table 8.
| |
| | |
| [[file:Aprepitant CS5.png|none|400px]]
| |
| | |
| The antiemetic activity of Aprepitant was evaluated based on the following endpoints:
| |
| *Primary endpoint:
| |
| **Complete response (defined as no emetic episodes and no use of rescue therapy) in the overall phase (0 to 120 hours post-chemotherapy)
| |
| | |
| *Other prespecified endpoints:
| |
| **no emesis (defined as no emetic episodes regardless of use of rescue therapy)
| |
| **no nausea (maximum VAS <5 mm on a 0 to 100 mm scale)
| |
| **no significant nausea (maximum VAS <25 mm on a 0 to 100 mm scale)
| |
| **complete protection (defined as no emetic episodes, no use of rescue therapy, and a maximum nausea visual analogue scale [VAS] score <25 mm on a 0 to 100 mm scale)
| |
| complete response during the acute and delayed phases.
| |
| | |
| A summary of the key results from this study is shown in Table 9.
| |
| | |
| [[file:Aprepitant CS6.png|none|400px]]
| |
| | |
| In this study, a statistically significantly (p=0.015) higher proportion of patients receiving the aprepitant regimen (51%) in Cycle 1 had a complete response (primary endpoint) during the overall phase compared with patients receiving standard therapy (42%). The difference between treatment groups was primarily driven by the “No Emesis Endpoint”, a principal component of this composite primary endpoint. In addition, a higher proportion of patients receiving the aprepitant regimen in Cycle 1 had a complete response during the acute (0-24 hours) and delayed (25-120 hours) phases compared with patients receiving standard therapy; however, the treatment group differences failed to reach statistical significance, after multiplicity adjustments.
| |
| | |
| *Patient-Reported Outcomes: In a phase III study in patients receiving moderately emetogenic chemotherapy, the impact of nausea and vomiting on patients’ daily lives was assessed in Cycle 1 using the FLIE. A higher proportion of patients receiving the aprepitant regimen reported minimal or no impact on daily life (64% versus 56%). This difference between treatment groups was primarily driven by the “No Vomiting Domain” of this composite endpoint.
| |
| *Multiple-Cycle Extension: Patients receiving moderately emetogenic chemotherapy were permitted to continue into the Multiple-Cycle extension of the study for up to 3 additional cycles of chemotherapy. Antiemetic effect for patients receiving the aprepitant regimen is maintained during all cycles.
| |
| *Postmarketing Trial: In a postmarketing, multicenter, randomized, double-blind, parallel-group, clinical study in 848 cancer patients, the aprepitant regimen (N = 430) was compared with a standard of care therapy (N = 418) in patients receiving a moderately emetogenic chemotherapy regimen that included any IV dose of oxaliplatin, carboplatin, epirubicin, idarubicin, ifosfamide, irinotecan, daunorubicin, doxorubicin; cyclophosphamide IV (<1500 mg/m2); or cytarabine IV (>1 g/m2).
| |
| | |
| Of the 430 patients who were randomized to receive the aprepitant regimen, approximately 76% were women and 24% were men. The distribution by race was 67% White, 6% Black or African American, 11% Asian, and 12% multiracial. Classified by ethnicity, 36% were Hispanic and 64% were non-Hispanic. The aprepitant-treated patients in this clinical study ranged from 22 to 85 years of age, with a mean age of 57 years; approximately 59% of the patients were 55 years or older with 32 patients being over 74 years. Patients receiving the aprepitant regimen were receiving chemotherapy for a variety of tumor types including 50% with breast cancer, 21% with gastrointestinal cancers including colorectal cancer, 13% with lung cancer and 6% with gynecological cancers.
| |
| | |
| The antiemetic activity of Aprepitant was evaluated based on no vomiting (with or without rescue therapy) in the overall period (0 to 120 hours post-chemotherapy) and complete response (defined as no vomiting and no use of rescue therapy) in the overall period.
| |
| | |
| A summary of the key results from this study is shown in Table 10.
| |
| | |
| [[file:Aprepitant CS7.png|none|400px]]
| |
| | |
| In this study, a statistically significantly higher proportion of patients receiving the aprepitant regimen (76%) in Cycle 1 had no vomiting during the overall phase compared with patients receiving standard therapy (62%). In addition, a higher proportion of patients receiving the aprepitant regimen (69%) in Cycle 1 had a complete response in the overall phase (0-120 hours) compared with patients receiving standard therapy (56%). In the acute phase (0 to 24 hours following initiation of chemotherapy), a higher proportion of patients receiving aprepitant compared to patients receiving standard therapy were observed to have no vomiting (92% and 84%, respectively) and complete response (89% and 80%, respectively). In the delayed phase (25 to 120 hours following initiation of chemotherapy), a higher proportion of patients receiving aprepitant compared to patients receiving standard therapy were observed to have no vomiting (78% and 67%, respectively) and complete response (71% and 61%, respectively).
| |
| | |
| In a subgroup analysis by tumor type, a numerically higher proportion of patients receiving aprepitant were observed to have no vomiting and complete response compared to patients receiving standard therapy. For gender, the difference in complete response rates between the aprepitant and standard regimen groups was 14% in females (64.5% and 50.3%, respectively) and 4% in males (82.2% and 78.2%, respectively) during the overall phase. A similar difference for gender was observed for the no vomiting endpoint.
| |
| | |
| ====Prevention of Postoperative Nausea and Vomiting (PONV)====
| |
| In two multicenter, randomized, double-blind, active comparator-controlled, parallel-group clinical studies (PONV Studies 1 and 2), aprepitant was compared with ondansetron for the prevention of postoperative nausea and vomiting in 1658 patients undergoing open abdominal surgery. Patients were randomized to receive 40 mg aprepitant, 125 mg aprepitant, or 4 mg ondansetron. Aprepitant was given orally with 50 mL of water 1 to 3 hours before anesthesia. Ondansetron was given intravenously immediately before induction of anesthesia. A comparison between the 125 mg dose and the 40 mg dose did not demonstrate any additional clinical benefit. The remainder of this section will focus on the results in the 40 mg aprepitant dose recommended for PONV.
| |
| | |
| Of the 564 patients who received 40 mg aprepitant, 92% were women and 8% were men; of these, 58% were White, 13% Hispanic American, 7% Multi-Racial, 14% Black, 6% Asian, and 2% Other. The age of patients treated with 40 mg aprepitant ranged from 19 to 84 years, with a mean age of 46.1 years. 46 patients were 65 years or older, with 13 patients being 75 years or older. The antiemetic activity of Aprepitant was evaluated during the 0 to 48 hour period following the end of surgery. The two pivotal studies were of similar design; however, they differed in terms of study hypothesis, efficacy analyses and geographic location. PONV Study 1 was a multinational study including the U.S., whereas, PONV Study 2 was conducted entirely in the U.S.
| |
| | |
| Efficacy measures in PONV Study 1 included:
| |
| *no emesis (defined as no emetic episodes regardless of use of rescue therapy) in the 0 to 24 hours following the end of surgery (primary)
| |
| *complete response (defined as no emetic episodes and no use of rescue therapy) in the 0 to 24 hours following the end of surgery (primary)
| |
| *no emesis (defined as no emetic episodes regardless of use of rescue therapy) in the 0 to 48 hours following the end of surgery (secondary)
| |
| *time to first use of rescue medication in the 0 to 24 hours following the end of surgery (exploratory)
| |
| *time to first emesis in the 0 to 48 hours following the end of surgery (exploratory).
| |
| | |
| A closed testing procedure was applied to control the type I error for the primary endpoints.
| |
| | |
| The results of the primary and secondary endpoints for 40 mg aprepitant and 4 mg ondansetron are described in Table 11:
| |
| | |
| [[file:Aprepitant CS8.png|none|400px]]
| |
| | |
| The use of aprepitant did not affect the time to first use of rescue medication when compared to ondansetron. However, compared to the ondansetron group, use of aprepitant delayed the time to first vomiting, as depicted in Figure 3.
| |
| | |
| [[file:Aprepitant CS9.png|none|400px]]
| |
| | |
| *Efficacy measures in PONV Study 2 included:
| |
| **complete response (defined as no emetic episodes and no use of rescue therapy) in the 0 to 24 hours following the end of surgery (primary)
| |
| **no emesis (defined as no emetic episodes regardless of use of rescue therapy) in the 0 to 24 hours following the end of surgery (secondary)
| |
| **no use of rescue therapy in the 0 to 24 hours following the end of surgery (secondary)
| |
| **no emesis (defined as no emetic episodes regardless of use of rescue therapy) in the 0 to 48 hours following the end of surgery (secondary).
| |
| **PONV Study 2 failed to satisfy its primary hypothesis that aprepitant is superior to ondansetron in the prevention of PONV as measured by the proportion of patients with complete response in the 24 hours following end of surgery.
| |
| | |
| The study demonstrated that both dose levels of aprepitant had a clinically meaningful effect with respect to the secondary endpoint “no vomiting” during the first 24 hours after surgery and showed that the use of 40 mg aprepitant was associated with a 16% improvement over ondansetron for the no vomiting endpoint.
| |
| | |
| [[file:Aprepitant CS10.png|none|400px]]
| |
| |howSupplied=No. 3854 — 80 mg capsules: White, opaque, hard gelatin capsule with “461” and “80 mg” printed radially in black ink on the body. They are supplied as follows:
| |
| *NDC 54868-5231-2 unit-of-use BiPack of 2
| |
| *NDC 54868-5231-3 unit-of-use BiPack of 4
| |
| *NDC 54868-5231-1 unit-dose package of 6.
| |
| |storage=Store at 20-25°C (68-77°F)
| |
| |packLabel=[[file:Aprepitant Appearance.png|none|400px]]
| |
| |alcohol=Alcohol-Aprepitant (patient information) interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
| |
| |brandNames=*[[Emend]]
| |
| }}
| |
| {{LabelImage
| |
| |fileName=Aprep PAckage.png
| |
| }}
| |
| {{LabelImage
| |
| |fileName=Aprep Package2.png
| |
| }}
| |