drug
(cytarabine hydrochloride + daunorubicin hydrochloride)
Marketedupdated 3mo agoby $JAZZ Jazz Pharmaceuticals plc
Approvedcommunity read0 votes
🐶 often sniffed alongside
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Trials studying (cytarabine hydrochloride + daunorubicin hydrochloride)
- phase1CPX-351 in Combination With Gemtuzumab Ozogamicin in Newly Diagnosed AML
- phase1Vyxeos Plus Gilteritinib in Relapsed or Refractory, FLT3-Mutated AML
- —VYxeoS Liposomal Italian Observational Study iN the Real Practice
- phase1Vyxeos® With Clofarabine for Pediatric AML
- N/AA Bioequivalence Study of (Cytarabine: Daunorubicin) Liposome for Injection
Patent cliff
source: FDA Orange Bookfirst barrier falls
Jan 23, 2027
165 days
Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.
patents (15)
- Apr 15, 2033patentUS 10028912*PED
- Apr 15, 2033patentUS 10166184*PED
- Apr 15, 2033patentUS 10835492*PED
- Oct 15, 2032formulationUS 10028912
- Oct 15, 2032formulationUS 10166184
- Oct 15, 2032method-of-use (U-3150)US 10835492
- Oct 1, 2029patentUS 8092828*PED3.1y
- Apr 1, 2029method-of-use (U-3147)US 80928282.6y
- Mar 14, 2028patentUS 8022279*PED1.6y
- Sep 14, 2027formulationUS 80222791.1y
- Jul 23, 2027patentUS 7850990*PED346d
- Jul 23, 2027patentUS 9271931*PED346d
- Jan 23, 2027formulationUS 7850990165d
- Jan 23, 2027formulationUS 9271931165d
- Jun 7, 2026formulationUS 8518437
FDA exclusivities (2)
- Sep 30, 2028PEDPediatric (6mo bonus)2.1y
- Mar 30, 2028ODE-350Orphan Drug (7y)1.6y
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