drug
cobicistat
Marketedupdated 5mo agoby $GILD GILEAD SCIENCES, INC.
Approvedcommunity read0 votes
🐶 often sniffed alongside
top 5all catalysts(0)
nothing on the calendar yet
Trials studying cobicistat
- phase2A Study of Revumenib in R/R Leukemias Including Those With an MLL/KMT2A Gene Rearrangement or NPM1 Mutation
- phase4A Study to Provide Continued Access to Study Drug to Children and Adolescents Who Have Completed Clinical Studies Involving Gilead HIV Treatments
- phase3Study of Cobicistat-Boosted Atazanavir (ATV/co), Cobicistat-Boosted Darunavir (DRV/co) and Emtricitabine/Tenofovir Alafenamide (F/TAF) in Children With HIV
- phase1A Study of the Effects of Food and Cobicistat on Plixorafenib Pharmacokinetics in Healthy Participants.
- —Pharmacokinetic Properties of Antiretroviral and Anti-Tuberculosis Drugs During Pregnancy and Postpartum
- phase2ProSTAR: A Study Evaluating CPI-1205 in Patients With Metastatic Castration Resistant Prostate Cancer
- phase4A Study to Evaluate the Pharmacokinetics (PK) of Darunavir (DRV) and Cobicistat (COBI) After a Single Oral Administration of Darunavir/Cobicistat Fixed-Dose Combination in Healthy Japanese Adult Participants
- phase1Study to Evaluate the Relative Bioavailability of Fixed-dose Combination Tablet Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (D/C/F/TAF) as a Whole Tablet, as a Split Tablet, and as Crushed Tablet in Healthy Adult Participants
Patent cliff
source: FDA Orange Bookfirst barrier falls
Sep 3, 2029
~2.9 years out
Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.
patents (8)
- Apr 6, 2033patentUS 10039718*PED
- Apr 6, 2033patentUS 10039718*PED
- Oct 6, 2032formulationUS 10039718
- Oct 6, 2032formulationUS 10039718
- Mar 3, 2030patentUS 8148374*PED3.4y
- Mar 3, 2030patentUS 8148374*PED3.4y
- Sep 3, 2029compositionUS 81483742.9y
- Sep 3, 2029compositionUS 81483742.9y
FDA exclusivities (1)
- Aug 22, 2026ODE-260Orphan Drug (7y)
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