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Ozekibart

Research only

unresectable or metastatic conventional chondrosarcoma

Published evidence

1 publications1 exact-program0 related2 context / correction notes

Review publications

Program details

Filing reports BLA acceptance for ozekibart in conventional chondrosarcoma and an April 14, 2027 FDA target.

Program names
ozekibart / INBRX-109
Modality
Antibody
Indication
unresectable or metastatic conventional chondrosarcoma
Associated trial
NCT04950075
FDA target
April 14, 2027Date-only guidance; not a trading cutoff.

Publications 1

Evidence is grouped by its relationship to this program.

Search PubMed

Publication notes explain the evidence behind this program. PubMed / NCBI data notice

Coverage & interpretation
  • The selected primary paper combines preclinical and exploratory phase 1 evidence.
  • No standalone randomized ChonDRAgon results publication is included in this bounded seed.

Exact program / indication

1 record
Exact programhuman clinicalPMID 37265425

Preclinical Characterization and Phase I Trial Results of INBRX-109, A Third-Generation, Recombinant, Humanized, Death Receptor 5 Agonist Antibody, in Chondrosarcoma.

Clinical cancer research : an official journal of the American Association for Cancer Research · 2023-08-15

This paper combines preclinical DR5-antibody characterization with exploratory phase 1 chondrosarcoma findings. It reports antitumor activity and safety observations in small cohorts and identifies the later randomized ChonDRAgon trial as further evaluation.

Program relevance

The paper directly studies INBRX-109 in chondrosarcoma, including phase 1 cohorts; it predates randomized ChonDRAgon results.

Formulation / population: Intravenous INBRX-109, the DR5 agonist antibody later named ozekibart.

  • Mixed preclinical and phase 1 clinical evidence.
  • Not a randomized ChonDRAgon phase 2 results publication.

Clinical Trial, Phase I / Journal Article / Research Support, N.I.H., Extramural / Research Support, Non-U.S. Gov't

Sources

Publication and retrieval dates are shown separately. Market rules determine which evidence can resolve an outcome.

sec-filingwww.sec.gov
Filing reports BLA acceptance for ozekibart in conventional chondrosarcoma and an April 14, 2027 FDA target.
Published
Jun 15, 2026
Retrieved
2026-10-30 02:09:48 UTC
sec-exhibitwww.sec.gov
Sponsor describes ozekibart as a tetravalent DR5 agonist antibody and identifies the ChonDRAgon registrational study.
Published
Jun 15, 2026
Retrieved
2026-10-30 02:09:48 UTC
clinical-trial-registryclinicaltrials.gov
Registry identifies the associated compound, condition and sponsor; trial completion is separate from FDA action.
Published
Not supplied
Retrieved
2026-10-30 02:09:48 UTC

Research identity and publications do not establish regulatory approval, clinical suitability or an executable market. Read the limits