Study of NGM707 in Combination With Pembrolizumab in Advanced or Metastatic Solid Tumor Malignancies
- Sponsor
- NGM Biopharmaceuticals, Inc
- Study ID
- NCT07511972
- Phase
- PHASE2
- Status
- Withdrawn
Conditions
- CRC
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- NGM707 plus pembrolizumab — DRUGDrug: NGM707 NGM707 will be administered intravenously (IV) every 3 weeks in a 21 day cycle. Drug: pembrolizumab Pembrolizumab will be administered intravenously (IV) every 3 weeks in a 21 day cycle.
Study Details
Study of NGM707 in Combination With Pembrolizumab in Advanced or Metastatic Solid Tumor Malignancies
Key Dates
- Start date
- Nov 14, 2023
- Status verified
- Mar 2026
- Primary completion
- Dec 31, 2024
- Completion
- Sep 30, 2025
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: NGM707 Combination Cohort ANGM707 with pembrolizumab in MSS CRC
Primary Outcome Measure
Objective response rate (ORR) as per RECIST v1.1 [ Time Frame: Baseline up to approximately 24 months ]
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