Brexanolone
Jump to navigation
Jump to search
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Zach Leibowitz [2]
Disclaimer
WikiDoc MAKES NO GUARANTEE OF VALIDITY. WikiDoc is not a professional health care provider, nor is it a suitable replacement for a licensed healthcare provider. WikiDoc is intended to be an educational tool, not a tool for any form of healthcare delivery. The educational content on WikiDoc drug pages is based upon the FDA package insert, National Library of Medicine content and practice guidelines / consensus statements. WikiDoc does not promote the administration of any medication or device that is not consistent with its labeling. Please read our full disclaimer here.
Black Box Warning
|
EXCESSIVE SEDATION AND SUDDEN LOSS OF CONSCIOUSNESS
See full prescribing information for complete Boxed Warning.
Patients treated with brexanolone are at risk of excessive sedation or sudden loss of consciousness during administration. Because of the risk of serious harm, patients must be monitored for excessive sedation and sudden loss of consciousness and have continuous pulse oximetry monitoring. Patients must be accompanied during interactions with their child(red). Because of these risks, brexanolone is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the Zulresso REMS.
|
Overview
Brexanolone is a neuroactive steroid gamma-aminobutyric acid (GABA) A receptor positive modulator that is FDA approved for the treatment of postpartum depression (PPD) in adults. There is a Black Box Warning for this drug as shown here. Common adverse reactions include sedation/somnolence, dry mouth, loss of consciousness, and flushing/hot flush.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
Brexanolone is indicated for the treatment of postpartum depression (PPD) in adults.
Injection: 100 mg/20 mL (5 mg/mL) single-dose vial.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information regarding brexanolone Off-Label Guideline-Supported Use and Dosage (Adult) in the drug label.
Non–Guideline-Supported Use
There is limited information regarding brexanolone Off-Label Non-Guideline-Supported Use and Dosage (Adult) in the drug label.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
The safety and effectiveness of brexanolone in pediatric patients have not been established.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
There is limited information regarding brexanolone Off-Label Guideline-Supported Use and Dosage (Pediatric) in the drug label.
Non–Guideline-Supported Use
There is limited information regarding brexanolone Off-Label Non-Guideline-Supported Use and Dosage (Pediatric) in the drug label.
Contraindications
None.
Warnings
|
EXCESSIVE SEDATION AND SUDDEN LOSS OF CONSCIOUSNESS
See full prescribing information for complete Boxed Warning.
Patients treated with brexanolone are at risk of excessive sedation or sudden loss of consciousness during administration. Because of the risk of serious harm, patients must be monitored for excessive sedation and sudden loss of consciousness and have continuous pulse oximetry monitoring. Patients must be accompanied during interactions with their child(red). Because of these risks, brexanolone is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the Zulresso REMS.
|
Excessive Sedation and Sudden Loss of Consciousness
- In clinical studies, brexanolone caused sedation and somnolence that required dose interruption or reduction in some patients during the infusion (5% of brexanolone-treated patients compared to 0% of placebo-treated patients). Some patients were also reported to have loss of consciousness or altered state of consciousness during the brexanolone infusion (4% of the brexanolone-treated patients compared with 0% of the placebo-treated patients). Time to full recovery from loss or altered state of consciousness, after dose interruption, ranged from 15 to 60 minutes. A healthy 55-year-old man participating in a cardiac repolarization study experienced severe somnolence and <1 minute of apnea while receiving two times the maximum recommended dosage of brexanolone (180 mcg/kg/hour). All patients with loss of or altered state of consciousness recovered with dose interruption.
- There was no clear association between loss or alteration of consciousness and pattern or timing of dose. Not all patients who experienced a loss or alteration of consciousness reported sedation or somnolence before the episode.
- During the infusion, monitor patients for sedative effects every 2 hours during planned, non-sleep periods. Immediately stop the infusion if there are signs or symptoms of excessive sedation.
- After symptoms resolve, the infusion may be resumed at the same or lower dose as clinically appropriate.
- Immediately stop the infusion if pulse oximetry reveals hypoxia. After hypoxia, the infusion should not be resumed.
- Patients should be cautioned against engaging in potentially hazardous activities requiring mental alertness, such as driving after infusion until any sedative effects of brexanolone have dissipated. Patients must be accompanied during interactions with their child(ren) while receiving the infusion because of the potential for excessive sedation and sudden loss of consciousness.
- Concomitant use of opioids, antidepressants, or other CNS depressants such as benzodiazepines or alcohol may increase the likelihood or severity of adverse reactions related to sedation.
- Because of the risk of serious harm resulting from excessive sedation or sudden loss of consciousness, brexanolone is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the Zulresso REMS.
Brexanolone Risk Evaluation and Mitigation Strategy (REMS)
- Brexanolone is available only through a restricted program under a REMS called the Zulresso REMS because excessive sedation or sudden loss of consciousness can result in serious harm.
- Notable requirements of the Zulresso REMS include the following:
- Healthcare facilities must enroll in the program and ensure that brexanolone is only administered to patients who are enrolled in the Zulresso REMS.
- Pharmacies must be certified with the program and must only dispense brexanolone to healthcare facilities who are certified in the Zulresso REMS.
- Patients must be enrolled in the Zulresso REMS prior to administration of brexanolone.
- Wholesalers and distributors must be registered with the program and must only distribute to certified healthcare facilities and pharmacies.
- Further information, including a list of certified healthcare facilities, is available at WWW.ZULRESSOREMS.COM or 1-844-472-4379.
Suicidal Thoughts and Behaviors
- In pooled analyses of placebo-controlled trials of chronically administered antidepressant drugs (SSRIs and other antidepressant classes) that included approximately 77,000 adult patients and 4,500 pediatric patients, the incidence of suicidal thoughts and behaviors in antidepressant-treated patients age 24 years and younger was greater than in placebo-treated patients. There was considerable variation in risk of suicidal thoughts and behaviors among drugs, but there was an increased risk identified in young patients for most drugs studied. There were differences in absolute risk of suicidal thoughts and behaviors across the different indications, with the highest incidence in patients with major depressive disorder (MDD). The drug-placebo differences in the number of cases of suicidal thoughts and behaviors per 1000 patients treated are provided in TABLE 1.
- Brexanolone does not directly affect monoaminergic systems. Because of this and the comparatively low number of exposures to brexanolone, the risk of developing suicidal thoughts and behaviors with brexanolone is unknown. Consider changing the therapeutic regimen, including discontinuing brexanolone, in patients whose depression becomes worse or who experience emergent suicidal thoughts and behaviors.
Adverse Reactions
Clinical Trials Experience
- Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.
- The data described below reflect exposure to brexanolone in 140 patients with postpartum depression (PPD). A titration to a target dosage of 90 mcg/kg/hour was evaluated in 102 patients and a titration to a target dose of 60 mcg/kg/hour was evaluated in 38 patients. Patients were then followed for 4 weeks.
- The most common adverse reactions (incidence ≥5% and at least twice the rate of placebo) were sedation/somnolence, dry mouth, loss of consciousness, and flushing/hot flush (TABLE 2).
Adverse Reactions Leading to Discontinuation, Dosage Interruption, or Dosage Reduction
- In the pooled placebo controlled-studies, the incidence of patients who discontinued due to any adverse reaction was 2% of brexanolone-treated patients compared to 1% of placebo-treated patients. The adverse reactions leading to treatment discontinuation in brexanolone-treated patients were sedation-related (loss of consciousness, vertigo, syncope, and presyncope) or infusion site pain.
- In the pooled placebo controlled-studies, the incidence of patients who had an interruption or reduction of the dosage due to any adverse reaction was 7% of brexanolone-treated patients compared to 3% of placebo-treated patients. The adverse reactions leading to dose reduction or interruption in brexanolone-treated patients were sedation-related (loss of consciousness, syncope, somnolence, dizziness, fatigue), infusion site events, changes in blood pressure, or medication error due to infusion pump malfunction. Three brexanolone-treated patients who had a dosage interruption because of loss of consciousness subsequently resumed and completed treatment after resolution of symptoms; two patients who had dosage interruption because of loss of consciousness did not resume the infusion.
- TABLE 2 presents the adverse reactions that occurred in brexanolone-treated PPD patients at a rate of at least 2% and at a higher rate than in the placebo-treated patients during the 60-hour treatment period.
Postmarketing Experience
There is limited information regarding Brexanolone Postmarketing Experience in the drug label.
Drug Interactions
CNS Depressants
- Concomitant use of brexanolone with CNS depressants (e.g., opioids, benzodiazepines) may increase the likelihood or severity of adverse reactions related to sedation.
Antidepressants
- In the placebo-controlled studies, a higher percentage of brexanolone-treated patients who used concomitant antidepressants reported sedation-related events.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA): Pregnancy Exposure
- There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antidepressants during pregnancy. Healthcare providers are encouraged to register patients by calling the National Pregnancy Registry for Antidepressants at 1-844-405-6185 or visiting online at HTTPS://WOMENSMENTALHEALTH.ORG/CLINICAL-AND-RESEARCH-PROGRAMS/PREGNANCYREGISTRY/ANTIDEPRESSANTS/.
Risk Summary
- Based on findings from animal studies of other drugs that enhance GABAergic inhibition, brexanolone may cause fetal harm. There are no available data on brexanolone use in pregnant women to determine a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. In animal reproduction studies, malformations were not seen in rats or rabbits at plasma levels up to 5 and 6 times the maximum recommended human dose (MRHD), respectively. Developmental toxicities were seen in the fetuses of rats and rabbits at 5 and ≥3 times the plasma levels at the MRHD, respectively. Reproductive toxicities were seen in rabbits at ≥3 times the plasma levels at the MRHD. These effects were not seen in rats and rabbits at 2 and 1.2 times the plasma levels at the MRHD. Brexanolone administered to pregnant rats during pregnancy and lactation resulted in lower pup survival at doses which were associated with ≥2 times the plasma levels at the MRHD and a neurobehavioral deficit in female offspring at 5 times the plasma levels at the MRHD. These effects were not seen at 0.8 times and 2 times the plasma levels at the MRHD, respectively.
- In published animal studies, administration of other drugs that enhance GABAergic inhibition to neonatal rats caused widespread apoptotic neurodegeneration in the developing brain. The window of vulnerability to these changes in rats (postnatal days 0-14) corresponds to the period of brain development that takes place during the third trimester of pregnancy in humans.
- The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.
Animal Data
- In pregnant rats and rabbits, no malformations were seen when brexanolone was given during the period of organogenesis at continuous intravenous doses up to 60 and 30 mg/kg/day, respectively. These doses were associated with maternal plasma levels 5 and 6 times the plasma levels at the MRHD of 90 mcg/kg/hour, in rats and rabbits, respectively. In rats, a decrease in fetal body weights was seen at 60 mg/kg/day (5 times the plasma level at the MRHD). In rabbits, increased numbers of late resorptions and a decrease in fetal body weights were seen at doses equal to and greater than 15 mg/kg/day (3 times the plasma levels at the MRHD) with fewer live fetuses and a higher post implantation loss seen at 30 mg/kg/day (6 times the plasma levels at the MRHD) in the presence of maternal toxicity (decreased food consumption and decreased body weight gain and/or body weight loss). Effects in rats and rabbits were not seen at 2 and 1.2 times the plasma levels at the MRHD, respectively.
- When brexanolone was administered to pregnant rats by continuous intravenous administration at 30 and 60 mg/kg/day (2 and 5 times plasma levels at the MRHD, respectively) during the period of organogenesis and throughout pregnancy and lactation, increased numbers of dead pups and fewer live pups at birth were seen. This effect was not seen at 0.8 times the plasma levels at the MRHD. Decreased pup viability between postnatal day 0 and 4 in the presence of maternal toxicity (decreased body weight gain and food consumption during lactation) was seen at 5 times the plasma levels at the MRHD. These effects were not seen at 2 times the plasma levels at the MRHD. A neurobehavioral deficit, characterized by slower habituation in the maximal startle response in the auditory startle test, was seen in female offspring of dams dosed at 5 times the plasma levels at the MRHD. This effect was not seen at 2 times the plasma levels at the MRHD.
Pregnancy Category (AUS):
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Brexanolone in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Brexanolone during labor and delivery.
Nursing Mothers
Risk Summary
- Available data from a lactation study in 12 women indicate that brexanolone is transferred to breastmilk in nursing mothers. However, the relative infant dose (RID) is low, 1% to 2% of the maternal weight-adjusted dosage (see DATA). Also, as brexanolone has low oral bioavailability (<5%) in adults, infant exposure is expected to be low. There were no reports of effects of brexanolone on milk production. There are no data on the effects of brexanolone on a breastfed infant. Available data on the use of brexanolone during lactation do not suggest a significant risk of adverse reactions to breastfed infants from exposure to brexanolone. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for brexanolone and any potential adverse effects on the breastfed child from brexanolone or from the underlying maternal condition.
Data
- A study was conducted in twelve healthy adult lactating women treated with intravenous brexanolone according to the recommended 60-hour dosing regimen (maximum dosage was 90 mcg/kg/hour). Concentrations of brexanolone in breast milk were at low levels (<10 ng/mL) in >95% of women by 36 hours after the end of the infusion of brexanolone. The calculated maximum relative infant dose for brexanolone during the infusion was 1% to 2%.
Pediatric Use
- The safety and effectiveness of brexanolone in pediatric patients have not been established.
Geriatic Use
PPD is a condition associated with pregnancy; there is no geriatric experience with brexanolone.
Gender
There is no FDA guidance on the use of Brexanolone with respect to specific gender populations.
Race
There is no FDA guidance on the use of Brexanolone with respect to specific racial populations.
Renal Impairment
- No dosage adjustment is recommended in patients with mild (eGFR 60 to 89 mL/minute/1.73 m2), moderate (eGFR 30 to 59 mL/minute/1.73 m2) or severe (eGFR 15 to 29 mL/minute/1.73 m2) renal impairment.
- Avoid use of brexanolone in patients with end stage renal disease (ESRD) with eGFR of < 15 mL/minute/1.73 m2 because of the potential accumulation of the solubilizing agent, betadex sulfobutyl ether sodium.
Hepatic Impairment
- Dosage adjustment in patients with hepatic impairment is not necessary. Modest increases in exposure to unbound brexanolone and modest decreases in exposure to total brexanolone were observed in patients with moderate to severe hepatic impairment (Child-Pugh≥7) with no associated change in tolerability.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Brexanolone in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Brexanolone in patients who are immunocompromised.
Administration and Monitoring
Administration
Recommended Dosage
- Administer brexanolone as a continuous intravenous (IV) infusion over a total of 60 hours (2.5 days) as follows:
- 0 to 4 hours: Initiate with a dosage of 30 mcg/kg/hour
- 4 to 24 hours: Increase dosage to 60 mcg/kg/hour
- 24 to 52 hours: Increase dosage to 90 mcg/kg/hour (a reduction in dosage to 60 mcg/kg/hour may be considered during this time period for patients who do not tolerate 90 mcg/kg/hour)
- 52 to 56 hours: Decrease dosage to 60 mcg/kg/hour
- 56 to 60 hours: Decrease dosage to 30 mcg/kg/hour
- If excessive sedation occurs at any time during the infusion, stop the infusion until the symptoms resolve. The infusion may be resumed at the same or lower dose as clinically appropriate.
Preparation and Storage Instructions
- Brexanolone is supplied in vials as a concentrated solution that requires dilution prior to administration. After dilution, the product can be stored in infusion bags under refrigerated conditions for up to 96 hours. However, given that the diluted product can be used for only 12 hours at room temperature, each 60-hour infusion will require the preparation of at least five infusion bags.
- Prepare according to the following steps using aseptic technique:
- Visually inspect the vials of brexanolone for particulate matter and discoloration prior to administration. Brexanolone is a clear, colorless solution. Do not use if the solution is discolored or particulate matter is present.
- The 60-hour infusion will generally require the preparation of five infusion bags. Additional bags will be needed for patients weighing ≥ 90 kg.
- For each infusion bag:
- Prepare and store in a polyolefin, non-DEHP, nonlatex bag, only. Dilute in the infusion bag immediately after the initial puncture of the drug product vial.
- Withdraw 20 mL of brexanolone from the vial and place in the infusion bag. Dilute with 40 mL of Sterile Water for Injection, and further dilute with 40 mL of 0.9% Sodium Chloride Injection (total volume of 100 mL) to achieve a target concentration of 1 mg/mL.
- Immediately place the infusion bag under refrigerated conditions until use.
- Diluted brexanolone storage instructions:
- If not used immediately after dilution, store under refrigerated conditions for up to 96 hours. Prolonged storage at room temperature may support adventitious microbial growth.
- Each prepared bag of diluted brexanolone may be used for up to 12 hours of infusion time at room temperature. Discard any unused brexanolone after 12 hours of infusion.
Administration Instructions
- Brexanolone must be diluted before administration. The following are important administration instructions:
- Use a programmable peristaltic infusion pump to ensure accurate delivery of brexanolone.
- Administer brexanolone via a dedicated line. Do not inject other medications into the infusion bag or mix with brexanolone.
- Fully prime infusion administration sets with admixture before inserting into the pump and connecting to the venous catheter.
- Use a PVC, non-DEHP, nonlatex infusion set. Do not use in-line filter infusion sets.
Recommendations in Patients with End Stage Renal Disease
- Avoid use of brexanolone in patients with end stage renal disease (ESRD) with eGFR of < 15 mL/minute/1.73 m2 because of the potential accumulation of the solubilizing agent, betadex sulfobutyl ether sodium.
Monitoring
Important Considerations Prior to Initiating and During Therapy
- A healthcare provider must be available on site to continuously monitor the patient, and intervene as necessary, for the duration of the brexanolone infusion.
- Monitor patients for hypoxia using continuous pulse oximetry equipped with an alarm. Assess for excessive sedation every 2 hours during planned, non-sleep periods.
- Initiate brexanolone treatment early enough during the day to allow for recognition of excessive sedation.
IV Compatibility
- Brexanolone is administered as a continuous intravenous (IV) infusion over a total of 60 hours (2.5 days).
Overdosage
Human Experience
- There is limited clinical trial experience regarding human overdosage with brexanolone. In premarketing clinical studies, two cases of accidental overdosage due to infusion pump malfunction resulted in transient loss of consciousness. Both patients regained consciousness approximately 15 minutes after discontinuation of the infusion without supportive measures. After full resolution of symptoms, both patients subsequently resumed and completed treatment. Overdosage may result in excessive sedation, including loss of consciousness and the potential for accompanying respiratory changes.
Management of Overdose
- In case of overdosage, stop the infusion immediately and initiate supportive measures as necessary. Brexanolone is rapidly cleared from plasma. Consult a Certified Poison Control Center at 1-800-222-1222 for latest recommendations.
Pharmacology
Mechanism of Action
- The mechanism of action of brexanolone in the treatment of PPD in adults is not fully understood, but is thought to be related to its positive allosteric modulation of GABAA receptors.
Structure
The molecular formula of brexanolone is C21H34O2. The relative molecular mass is 318.5 Da.
Pharmacodynamics
- Brexanolone potentiated GABA-mediated currents from recombinant human GABAA receptors in mammalian cells expressing α1β2γ2 receptor subunits, α4β3δ receptor subunits, and α6β3δ receptor subunits.
- Brexanolone exposure-response relationships and the time course of pharmacodynamics response are unknown.
Cardiac Electrophysiology
- The effect of brexanolone on the QT interval was evaluated in a Phase 1 randomized, placebo and positive controlled, double-blind, three-period crossover thorough QT study in 30 healthy adult subjects. At 1.9-times the exposure occurring at the highest recommended infusion rate (90 mcg/kg/hour), brexanolone did not prolong the QT interval to a clinically relevant extent.
Pharmacokinetics
- Brexanolone exhibited dose proportional pharmacokinetics over a dosage range of 30 mcg/kg/hour to 270 mcg/kg/hour (three times the maximum recommended dosage). Mean steady state exposure at 60 mcg/kg/hour and 90 mcg/kg/hour was around 52 ng/mL and 79 ng/mL, respectively.
Distribution
- The volume of distribution of brexanolone was approximately 3 L/kg, suggesting extensive distribution into tissues. Plasma protein binding was greater than 99% and is independent of plasma concentrations.
Elimination
- The terminal half-life of brexanolone is approximately 9 hours. The total plasma clearance of brexanolone is approximately 1 L/h/kg.
Metabolism
- Brexanolone is extensively metabolized by non-CYP based pathways via three main routes - keto-reduction (AKRs), glucuronidation (UGTs), and sulfation (SULTs). There are three major circulating metabolites that are pharmacologically inactive and do not contribute to the overall efficacy of brexanolone.
Excretion
- Following administration of radiolabeled brexanolone, 47% was recovered in feces (primarily as metabolites) and 42% in urine (with less than 1% as unchanged brexanolone).
Specific Populations
- No clinically significant differences in the pharmacokinetics of brexanolone were observed based on renal impairment (severe) study or hepatic impairment (mild, moderate, severe) study. The effect of end stage renal disease (ESRD, eGFR < 15 mL/minute/1.73 m2) on brexanolone pharmacokinetics is unknown. However, avoid use of brexanolone in patients with ESRD.
Drug Interaction Studies
- No studies were conducted to evaluate the effects of other drugs on brexanolone.
- No clinically significant differences in the pharmacokinetics of phenytoin (CYP2C9 substrate) were observed when it was used concomitantly with brexanolone.
Betadex Sulfobutyl Ether Sodium Pharmacokinetics
- Betadex sulfobutyl ether sodium is a solubilizing agent in brexanolone. In patients with severe renal impairment (eGFR 15-29 mL/minute/1.73 m2), betadex sulfobutyl ether sodium AUCinf increased 5.5-fold and Cmax increased 1.7-fold. Avoid use of brexanolone in patients with ESRD.
Nonclinical Toxicology
Carcinogenesis, Mutagenesis, Impairment of Fertility
Carcinogenesis
- Carcinogenicity studies of brexanolone have not been performed.
Mutagenesis
- Brexanolone was not genotoxic when tested in an in vitro microbial mutagenicity (Ames) assay, an in vitro micronucleus assay in human peripheral blood lymphocytes, and an in vivo rat bone marrow micronucleus assay.
Impairment of Fertility
- Treatment of female and male rats with brexanolone at doses equal to and greater than 30 mg/kg/day, which is associated with 2 times the plasma levels at the maximum recommended human dose (MRHD) of 90 mcg/kg/hour, caused impairment of female and male fertility and reproduction. In female rats, brexanolone was associated with decreased mating and fertility indices, an increase in number of days to mating, prolonged/irregular estrous cycles, an increase in the number of early resorptions, and post implantation loss. Reversal of effects in females was observed following a 28-day recovery period. In male rats, brexanolone was associated with decreased mating and fertility indices, decreased conception rate, lower prostate, seminal vesicle, and epididymis weight, as well as decreased sperm numbers. Impaired female and male fertility and reproduction were not observed at 0.8 times the MRHD.
Clinical Studies
- The efficacy of brexanolone in the treatment of postpartum depression (PPD) was demonstrated in two multicenter, randomized, double-blind, placebo-controlled studies (referred to as Studies 1 and 2) in women (18 to 45 years) with PPD who met the Diagnostic and Statistical Manual of Mental Disorders criteria for a major depressive episode (DSM-IV) with onset of symptoms in the third trimester or within 4 weeks of delivery. In these studies, patients received a 60-hour continuous intravenous infusion of brexanolone or placebo and were then followed for 4 weeks. Study 1 (NCT02942004) included patients with severe PPD (Hamilton Depression Rating Scale (HAM-D) score ≥ 26), and Study 2 (NCT02942017) included patients with moderate PPD (HAM-D score of 20 to 25). A titration to the recommended target dosage of 90 mcg/kg/hour was evaluated in both studies (patients received 30 mcg/kg/hour for 4 hours, 60 mcg/kg/hour for 20 hours, 90 mcg/kg/hour for 28 hours, followed by a taper to 60 mcg/kg/hour for 4 hours and then 30 mcg/kg/hour for 4 hours). A titration to a target dosage of 60 mcg/kg/hour (patients received 30 mcg/kg/hour for 4 hours, 60 mcg/kg/hour for 52 hours, then 30 mcg/kg/hour for 4 hours) was also evaluated in Study 1.
- Demographic and baseline disease characteristics were generally similar across treatment groups in the pooled Studies 1 and 2. Most patients were White (63%) or Black (34%); 18% of patients identified as Hispanic or Latina; the average age of women receiving brexanolone was 28 years. Most patients (76%) had onset of PPD symptoms within 4 weeks after delivery, with the remainder having onset during the third trimester. Baseline oral antidepressant use was reported for 23% of patients.
- The primary endpoint was the mean change from baseline in depressive symptoms as measured by the HAM-D total score at the end of the infusion (Hour 60). A pre-specified secondary efficacy endpoint was the mean change from baseline in HAM-D total score at Day 30. In both placebo-controlled studies, titration to a target dose of brexanolone 90 mcg/kg/hour was superior to placebo in improvement of depressive symptoms. In a group of 38 patients in Study 1, a brexanolone titration to a target dose of 60 mcg/kg/hour was also superior to placebo in improvement of depressive symptoms.
- Examination of subgroups by race did not suggest differences in response.
Time Course of Treatment Response
- FIGURE 1 shows the time course of response for the brexanolone 90 mcg/kg/hour-target and 60 mcg/kg/hour-target groups compared to the placebo group for Study 1.
How Supplied
- Brexanolone injection is supplied as 100 mg brexanolone in 20 mL (5 mg/mL) single-dose vials containing a sterile, preservative-free, clear, colorless solution.
Storage
- Store the undiluted brexanolone product at 2°C to 8°C (36°F to 46°F). Do not freeze. Store protected from light.
- The diluted product in the infusion bag can be used at room temperature for up to 12 hours. If the diluted product is not used immediately after dilution, store under refrigerated conditions for up to 96 hours.
Images
Drug Images
{{#ask: Page Name::Brexanolone |?Pill Name |?Drug Name |?Pill Ingred |?Pill Imprint |?Pill Dosage |?Pill Color |?Pill Shape |?Pill Size (mm) |?Pill Scoring |?NDC |?Drug Author |format=template |template=DrugPageImages |mainlabel=- |sort=Pill Name }}
Package and Label Display Panel
{{#ask: Label Page::Brexanolone |?Label Name |format=template |template=DrugLabelImages |mainlabel=- |sort=Label Page }}
Patient Counseling Information
- Advise the patient to read the FDA-approved patient labeling (MEDICATION GUIDE).
Excessive Sedation and Sudden Loss of Consciousness
- Patients may experience loss of consciousness or altered state of consciousness during the brexanolone infusion. Advise patients to report signs of excessive sedation that may occur during the infusion. Patients must not be the primary caregiver of dependents and must be accompanied during interactions with their child(red).
Zulresso Risk Evaluation and Mitigation Strategy (REMS)
- Brexanolone is available only through a restricted program called the Zulresso REMS.
- Inform the patient of the following notable requirements:
- Patients must be enrolled in the Zulresso REMS Program prior to administration.
- Patients must be monitored during administration of brexanolone and report any signs and symptoms of excessive sedation to a healthcare provider.
Potential for Abuse
- Advise patients that brexanolone can be abused or lead to dependence.
Concomitant Medications
- Caution patients that opioids or other CNS depressants, such as benzodiazepines, taken in combination with brexanolone may increase the severity of sedative effects.
Suicide Thoughts and Behaviors
- Advise patients and caregivers to look for the emergence of suicidal thoughts and behavior and instruct them to report such symptoms to the healthcare provider.
Pregnancy
- Advise women to notify their healthcare provider if they could possibly be pregnant prior to therapy with brexanolone. Advise pregnant women and females of reproductive potential of the potential risk to a fetus. Advise patients that there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to brexanolone during pregnancy.
Medication Guide
Precautions with Alcohol
- Concomitant use of alcohol may increase the likelihood or severity of adverse reactions related to sedation.
Brand Names
Look-Alike Drug Names
There is limited information regarding Brexanolone Look-Alike Drug Names in the drug label.
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.