Drugs / CI-8993
last change May 2023 re-read 3 minutes ago

CI-8993

Monoclonal antibody

Developed for
cancer
Investigated by
Curis, Inc.

Trials 1

202120222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT04475523 Sep 2020 → May 2023 cancer Curis, Inc. Completed No outcome recorded

News releases announcing trial results or a regulatory action · 3

DateIssuerRelease
2022-01-06 Curis, Inc. Results Curis Announces Updated Data with Additional Encouraging Clinical Activity in Phase 1/2 Study of CA-4948 Monotherapy in Targeted Patients with Relapsed or Refractory AML and MDS; and Initial Clinical Data from Phase 1 Study of CI-8993 in Patients with Relapsed or Refractory Solid Tumors curis.com ↗
2021-11-09 Curis, Inc. Results Curis Announces New Preclinical Data for CI-8993 at the Society for Immunotherapy of Cancer (SITC) Annual Meeting curis.com ↗
The abstract concluded that the study has validated 89 Zr-Df-CI-8993 for specific binding to huVISTA in-vivo.
2020-06-10 Curis, Inc. Regulatory Curis Announces FDA Clearance of IND Application for CI-8993, the First-In-Class Monoclonal Anti-VISTA Antibody curis.com ↗
Curis, Inc. (NASDAQ: CRIS), a biotechnology company focused on the development of innovative therapeutics for the treatment of cancer, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for CI-8993, the first-in-class monoclonal anti-VISTA antibody.

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as CI-8993 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04475523 ↗
Modality Monoclonal antibody “CI-8993 is a fully human immunoglobulin (Ig) G1κ monoclonal antibody (mAb) against the VISTA ligand” NCT04475523 ↗
Route Intravenous “Patients will be administered CI-8993 intravenously at a planned infusion rate over 2 hours” NCT04475523 ↗