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Clinical trial

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

NCT06501625 is registered in ClinicalTrials.gov with Institut de Recherches Internationales Servier as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

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
Lead sponsor
Institut de Recherches Internationales Servier
Phase
Phase 1/2
Overall status
Active, not recruiting
Start date
December 16, 2024
Completion date
September 13, 2027
Enrollment
55 (actual)
Sites
38

Conditions

As the registry lists them; a condition with its own page is linked.

locally advanced, unresectable or metastatic cholangiocarcinoma with an idh1 mutation