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  1. pharmadog
  2. ›drugs
  3. ›POMALIDOMIDE
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POMALIDOMIDE

Marketedupdated 3mo ago
by Celgene Corp
Approved
community read0 votes

🐶 often sniffed alongside

top 3
  • tagApproval16 co-mentions · 8 sources
  • tagSmall Molecule8 co-mentions · 8 sources
  • companyHetero Labs Ltd2 co-mentions · 2 sources

all catalysts(5)

approval · 5
Jan 26, 2022
approval
5y ago
POMALIDOMIDE — FDA approval
POMALIDOMIDE
→
Sep 26, 2024
approval
2y ago
POMALIDOMIDE — FDA approval
POMALIDOMIDE
→
Aug 5, 2025
approval
1y ago
POMALIDOMIDE — FDA approval
POMALIDOMIDE
→
Oct 17, 2025
approval
10mo ago
POMALIDOMIDE — FDA approval
POMALIDOMIDE
→
Dec 29, 2025
approval
8mo ago
POMALIDOMIDE — FDA approval
POMALIDOMIDE
→

Trials studying POMALIDOMIDE

  • phase2A Study to Investigate the Safety and Efficacy of Belantamab for the Treatment of Multiple Myeloma When Used as Monotherapy and in Combination Treatmentsrecruitingn=123
  • phase2AZD0305 as Monotherapy or in Combination With Anticancer Agents in Participants With Multiple Myelomarecruitingn=226
  • phase1A Study of an MMSET Inhibitor in Patients With Relapsed and Refractory Multiple Myelomarecruitingn=165
  • phase1A Study Evaluating the Safety, Pharmacokinetics, and Activity of Cevostamab in Participants With Relapsed or Refractory Multiple Myelomaactive not recruitingn=186
  • phase3Cevostamab in Combination With Pomalidomide and Dexamethasone Versus Standard of Care in Participants With Previously Treated Multiple Myelomarecruitingn=380
  • phase1A Study to Assess Adverse Events and Change in Disease Activity of Intravenously (IV) Infused Etentamig (ABBV-383) in Combination With Anti-Cancer Regimens for the Treatment of Adult Participants With Relapsed/Refractory Multiple Myelomaactive not recruitingn=283
  • phase2Comparing Lower Versus Standard Doses of Belantamab Mafodotin With Pomalidomide and Dexamethasone in Relapsed or Refractory Multiple Myeloma.not yet recruitingn=228
  • phase3A Study of the Efficacy and Safety of BCD-248 in Combination With Daratumumab in Patients With Relapsed or Refractory Multiple Myeloma (AMMADINA)recruitingn=390
more trials →

Patent cliff

source: FDA Orange Book
first barrier falls
Aug 30, 2026
10 days

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (24)

  • Dec 21, 2031patentUS 8828427*PED
  • Dec 21, 2031patentUS 8828427*PED
  • Dec 21, 2031patentUS 8828427*PED
  • Dec 21, 2031patentUS 8828427*PED
  • Jun 21, 2031compositionUS 88284274.8y
  • Jun 21, 2031compositionUS 88284274.8y
  • Jun 21, 2031compositionUS 88284274.8y
  • Jun 21, 2031compositionUS 88284274.8y
  • Nov 19, 2030patentUS 10555939*PED4.3y
  • Nov 19, 2030patentUS 10555939*PED4.3y
  • Nov 19, 2030patentUS 10555939*PED4.3y
  • Nov 19, 2030patentUS 10555939*PED4.3y
  • Nov 19, 2030patentUS 9993467*PED4.3y
  • Nov 19, 2030patentUS 9993467*PED4.3y
  • Nov 19, 2030patentUS 9993467*PED4.3y
  • Nov 19, 2030patentUS 9993467*PED4.3y
  • May 19, 2030formulationUS 105559393.7y
  • May 19, 2030formulationUS 105559393.7y
  • May 19, 2030formulationUS 105559393.7y
  • May 19, 2030formulationUS 105559393.7y
  • May 19, 2030formulationUS 99934673.7y
  • May 19, 2030formulationUS 99934673.7y
  • May 19, 2030formulationUS 99934673.7y
  • May 19, 2030formulationUS 99934673.7y

FDA exclusivities (16)

  • Nov 14, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 14, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 14, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 14, 2027PEDPediatric (6mo bonus)1.2y
  • May 14, 2027ODE-296Orphan Drug (7y)267d
  • May 14, 2027ODE-297Orphan Drug (7y)267d
  • May 14, 2027ODE-296Orphan Drug (7y)267d
  • May 14, 2027ODE-297Orphan Drug (7y)267d
  • May 14, 2027ODE-296Orphan Drug (7y)267d
  • May 14, 2027ODE-297Orphan Drug (7y)267d
  • May 14, 2027ODE-296Orphan Drug (7y)267d
  • May 14, 2027ODE-297Orphan Drug (7y)267d
  • Aug 30, 2026PCPC10d
  • Aug 30, 2026PCPC10d
  • Aug 30, 2026PCPC10d
  • Aug 30, 2026PCPC10d

News(1)

  • Novo escalates legal fight with Lilly; J&J reinforces ‘dominance’ in multiple myeloma
    Novo is seeking an injunction that would halt allegedly “misleading” obesity drug ads. Elsewhere, the FDA began reviewing a highly anticipated medicine and a veteran investor landed at an AI startup.
    biopharma_dive · 26d ago
brand
POMALIDOMIDE
generic
POMALIDOMIDE
indication
Kaposi Sarcoma
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 1h ago
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