A Study of BGC515 Capsules in Subjects With Advanced Solid Tumors
NCT06452160 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 103
Last updated 2024-08-09
Summary
The goal of this open-label, dose escalation and dose expansion Phase I clinical trial is to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of BGC515 administered once daily in 3 weeks cycles in solid tumor patients.
Conditions
- Mesothelioma
- Epithelioid Hemangioendothelioma(EHE)
- Solid Tumor
Interventions
- DRUG
-
BGC515
Capsules for oral administration
Sponsors & Collaborators
-
BridGene Biosciences Inc.
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-06-27
- Primary Completion
- 2027-06-30
- Completion
- 2027-12-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
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