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NCT05876754 · ClinicalTrials.gov record · last posted 2026-07-31

An Early Access Study of Ivosidenib in Patients With a Pretreated Locally Advanced or Metastatic Cholangiocarcinoma

Study acronym: ProvIDHe
StatusActive, Not Recruiting
PhasePhase 3
Started2023-05-03
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from the ClinicalTrials.gov record
A Phase 3b research study to consolidate the data that ivosidenib is safe and effective in adult patients with previously treated, locally advanced, or metastatic cholangiocarcinoma (CCA). All patients who meet inclusion criteria will be enrolled to receive ivosidenib tablets orally once daily for 28 day cycles, continuing as long as clinical benefit and consent for participation is maintained. There will be a minimum of 6 study visits from screening until the final follow-up, if one cycle of treatment is completed and consent is maintained through 18 months of follow-up. Each additional cycle completed will add one study visit, on the first day of each cycle.

Protocol amendment history 2 changes detected by DataLookout

2026-08-01
notable
Enrollment closed, study ongoing
2026-08-01
notable
Enrollment increased: 220 → 299 participants
Trial Details
NCT Number NCT05876754
Lead Sponsor Servier Affaires Médicales
Conditions Cholangiocarcinoma
Enrollment 299 participants
Start Date 2023-05-03
Primary Completion 2027-12-01 (estimated)
Study Completion 2027-12-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-31