Ivosidenib Plus Durvalumab and Gemcitabine/Cisplatin as First-Line Therapy in Participants With Locally Advanced or Metastatic Cholangiocarcinoma With an IDH1 Mutation

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

A PHASE 1B/2, SAFETY LEAD-IN AND DOSE-EXPANSION, OPEN LABEL, MULTICENTER TRIAL INVESTIGATING THE SAFETY, TOLERABILITY, AND PRELIMINARY ACTIVITY OF IVOSIDENIB IN COMBINATION WITH DURVALUMAB AND GEMCITABINE/CISPLATIN AS FIRST-LINE THERAPY IN PARTICIPANTS WITH LOCALLY ADVANCED, UNRESECTABLE OR METASTATIC CHOLANGIOCARCINOMA WITH AN IDH1 MUTATION

Intervention/treatment:
IVOSIDENIB / DURVALUMAB / CISPLATIN / GEMCITABINE
Medical condition:
CHOLANGIOCARCINOMA
Protocol code:
S095031-210
Control number:
297058
Status:
Recruiting
Approved:
June 05, 2025
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT06501625
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Institut de Recherches Internationales Servier (I.R.I.S.) Clinical Studies Department
Role
CONTACT
Phone:
+33 1 55 72 60 00
Sponsor
SERVIER CANADA INC

Locations

Princess Margaret Cancer Centre
Toronto, M5G 2C4
Recruiting
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