Phase Ib Trial of Infigratinib In Combination With Atezolizumab And Bevacizumab for The Second-Line Treatment of Advanced Cholangiocarcinoma With FGFR2 Fusion/Amplification
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT05510427
- Phase
- PHASE1
- Status
- Withdrawn
Conditions
- Cholangiocarcinoma
- Liver Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Infigratinib — DRUGGiven by PO
- Atezolizumab — DRUGGiven by (IV) vein
- Bevacizumab — DRUGGiven by (IV) vein
Study Details
To find the highest tolerable dose of infigratinib that can be given in combination with bevacizumab and atezolizumab to patients with advanced/metastatic CCA with a FGFR2 mutation.
Key Dates
- Start date
- Aug 7, 2023
- Status verified
- Aug 2023
- Primary completion
- Aug 7, 2023
- Completion
- Aug 7, 2023
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Part A (Dose Escalation)The first group of participants will receive the lowest dose level of infigratinib.
- Experimental: Part B (Dose Expansion)Participants will receive infigratinib at the recommended dose that was found in Part A.
Primary Outcome Measure
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0 [ Time Frame: through study completion; an average of 1 year. ]
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