Page updated ·next FDA decision on the calendar·Data as of Nov 5, 2026 5:03 AM ET
Ozekibart (INBRX-109) is an Inhibrx Biosciences, Inc. program in unresectable or metastatic conventional chondrosarcoma. Its PDUFA date is Apr 14, 2027, the FDA's goal date to complete review of the application. Every date links its source.
Indication under review: Unresectable or metastatic conventional chondrosarcoma. Sponsor: Inhibrx Biosciences, Inc. (INBX). Market-cap tier at the time we tracked it: Small. We track 1 catalyst event for this program: 1 upcoming and 0 in the record. A PDUFA date is the FDA's target date to complete review of a marketing application; a readout is the sponsor's expected date for clinical trial results. What a PDUFA date is · why we do not compare trial results across drugs.
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Questions
When is Ozekibart (INBRX-109)'s next FDA decision or readout?
Ozekibart (INBRX-109)'s PDUFA date is Apr 14, 2027. That is the FDA's goal date to complete review of the application; the agency can act earlier or extend it.
What happened at Ozekibart (INBRX-109)'s most recent FDA decision?
No FDA decision for Ozekibart (INBRX-109) is in our archive yet.
What is Ozekibart (INBRX-109) used for?
In our records Ozekibart (INBRX-109) is under review or in development for Unresectable or metastatic conventional chondrosarcoma.
Who makes Ozekibart (INBRX-109)?
Inhibrx Biosciences, Inc. (INBX).
Where does this data come from?
FDA announcements, sponsor press releases and SEC filings; every date on this page links its source.
Facts and dates only; not investment advice. Verify against primary FDA, SEC
and company filings. pdufa.bio is not affiliated with the FDA.
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