drug
ACYCLOVIR
Marketedupdated 3mo agoby Yiling Pharmaceutical Ltd
Approvedcommunity read0 votes
🐶 often sniffed alongside
top 6all catalysts(3)
Trials studying ACYCLOVIR
- phase2A Biomarker Study in Men With Localized Prostate Cancer Treated With Aglatimagene Besadenovec
- phase2Bortezomib and Rituximab for Patients With Waldenstrom's Macroglobulinemia
- phase2Time-limited Triplet Combination of Pirtobrutinib, Venetoclax, and Obinutuzumab for Patients With Treatment-naïve Chronic Lymphocytic Leukemia (CLL) or Richter Transformation (RT)
- phase1A Study of the Safety and Tolerability of ASP7317 in Senior Adults Who Are Losing Their Clear, Sharp Central Vision Due to Geographic Atrophy Secondary to Dry Age-related Macular Degeneration
- phase3A Study to Evaluate Efficacy, Safety, and Tolerability of Alemtuzumab in Pediatric Patients With RRMS With Disease Activity on Prior DMT
- phase3A Study to Compare Sitavig (Acyclovir) Buccal Tablet With a Placebo in the Treatment of Herpes Labialis in Participants Whose Immune System Works Normally
- phase3Phase 3 Study of ProstAtak® Immunotherapy With Standard Radiation Therapy for Localized Prostate Cancer
- phase2Randomized Controlled Trial of CAN-2409 Immunotherapy During Active Surveillance for Prostate Cancer (ULYSSES)
Patent cliff
source: FDA Orange Bookfirst barrier falls
Mar 23, 2027
214 days
Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.
patents (3)
- Jun 16, 2030formulationUS 85924343.8y
- Jun 3, 2027formulationUS 8747896286d
- Mar 23, 2027formulationUS 8791127214d
FDA exclusivities (1)
- Mar 29, 2026ODE-235Orphan Drug (7y)
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