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- N
- This edit created a new page (also see list of new pages)
- m
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20 May 2024
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N 20:36 | Retifanlimab-dlwr 3 changes history +8,754 [Rithish Nimmagadda (3×)] | |||
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20:36 (cur | prev) −296 Rithish Nimmagadda talk contribs | ||||
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20:33 (cur | prev) +86 Rithish Nimmagadda talk contribs | ||||
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20:31 (cur | prev) +8,964 Rithish Nimmagadda talk contribs (Created page with "{{DrugProjectFormSinglePage |authorTag={{VSRN}} |genericName=retifanlimab-dlwr |aOrAn=an |indicationType=treatment |indication=adults with metastatic or recurrent locally advanced Merkel cell carcinoma . Indication approved under accelerated approval based on tumor response rate and duration of response; continued approval may be contingent upon verification and description of clinical benefit in confirmatory trials. |adverseReactions=Adverse effects (≥10%): fatigue...") |
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20:32 | User:Rithish Nimmagadda 2 changes history +37 [Rithish Nimmagadda (2×)] | |||
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20:32 (cur | prev) +23 Rithish Nimmagadda talk contribs (→Pages Authored/Co-authored/Collaborated) | ||||
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20:18 (cur | prev) +14 Rithish Nimmagadda talk contribs (→Pages Authored/Co-authored/Collaborated) |
N 20:18 | Tofersen diffhist +3,936 Rithish Nimmagadda talk contribs (Created page with "{{DrugProjectFormSinglePage |authorTag={{VSRN}} |genericName=tofersen |aOrAn=an |drugClass=antisense oligonucleotide |indicationType=treatment |indication=amyotrophic lateral sclerosis (ALS) in adults who have a mutation in the superoxide dismutase 1 (SOD1) gene. |adverseReactions=he most common adverse reactions (≥ 10% of patients treated with tofersen and greater than placebo) were pain, fatigue, arthralgia, increased CSF white blood cell, and myalgia. |fdaLIADAdult=...") |
m 19:55 | Non-degenerate nucleotides per response element diffhist −51 Marshallsumter talk contribs (→Tabulation of counts) |
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03:56 | Leniolisib 2 changes history +3,116 [Alen Antony (2×)] | |||
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03:56 (cur | prev) +1,712 Alen Antony talk contribs | ||||
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03:38 (cur | prev) +1,404 Alen Antony talk contribs |