RecruitingPHASE1, PHASE2NCT06501625

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

Studying Cholangiocarcinoma

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Key facts

Sponsor
Institut de Recherches Internationales Servier
Intervention
Ivosidenib(drug)
Enrollment
52 target
Eligibility
18 years · All sexes
Timeline
20242027

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06501625 on ClinicalTrials.gov

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