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  1. pharmadog
  2. ›drugs
  3. ›Inqovi
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(cedazuridine + decitabine)

Marketedupdated 3mo ago
by Otsuka Pharmaceutical Co Ltd
Approved
community read0 votes

all catalysts(0)

nothing on the calendar yet

Trials studying (cedazuridine + decitabine)

  • phase2Roll-over Study for Patients Who Have Completed a Prior Novartis-sponsored Sabatolimab (MBG453) Study and Are Judged by the Investigator to Benefit From Continued Treatment With Sabatolimab.active not recruitingn=33
  • EP1Early Intervention in High Risk CCUSrecruitingn=108
  • phase1Inqovi Maintenance Therapy in Myeloid Neoplasmsactive not recruitingn=22
  • phase2STIMULUS MDS-US : Sabatolimab Added to HMA in Higher Risk MDSterminatedn=39

Patent cliff

source: FDA Orange Book
first barrier falls
Jul 7, 2027
323 days

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

patents (6)

  • Feb 24, 2041formulationUS 11963971
  • Feb 24, 2041method-of-use (U-2866)US 12239653
  • Oct 7, 2040formulationUS 12195496
  • Aug 22, 2030compositionUS 82688004.0y
  • Oct 16, 2028method-of-use (U-2867)US 86180752.2y
  • Oct 16, 2028compositionUS 95673632.2y

FDA exclusivities (1)

  • Jul 7, 2027ODE-316Orphan Drug (7y)323d

News(4)

  • Cullinan tees up J&J fight—and $100M payday—as Taiho-partnered drug hits phase 3 cancer goal
    Taiho Pharmaceutical and Cullinan Therapeutics have celebrated a second phase 3 victory for their small-molecule EGFR inhibitor, teeing up the partners to challenge Johnson & Johnson in a lung canc…
    fiercebiotech · 4d ago
  • Aardvark's next move after clinical hold; Alumis' verdict on Acelyrin asset
    Plus, news about Tenaya’s TN-401 and Taiho’s Inqovi. 📉 Aardvark to unblind rare disease trial following clinical hold: The FDA has placed a full clinical hold on the company's candidate for ...
    endpoints · 3mo ago
  • FDA Approves Decitabine/Cedazuridine Plus Venetoclax in Newly Diagnosed AML
    The FDA has approved oral decitabine/cedazuridine plus venetoclax for newly diagnosed AML unfit for intensive chemo, based on phase 2 ASCERTAIN-V data.
    onclive · 3mo ago
  • Dr Dinardo on the FDA Approval of Decitabine/Cedazuridine Plus Venetoclax in AML
    Courtney D. DiNardo, MD, MSCE, discusses the FDA approval of decitabine/cedazuridine plus venetoclax in acute myeloid leukemia.
    onclive · 3mo ago
brand
Inqovi
generic
(cedazuridine + decitabine)
indication
Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia)
phase
marketed
Data sources
ClinicalTrials.gov
last refreshed 8m ago
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