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A Phase 1 Dose Escalation/Dose Finding Study of NGM831 as Monotherapy and in Combination With Pembrolizumab or Pembrolizumab and NGM438 in Advanced or Metastatic Solid Tumors


Description

Study of NGM831 as Monotherapy and in Combination with Pembrolizumab or Pembrolizumab and NGM438 in Advanced or Metastatic Solid Tumors

Trial Eligibility

Inclusion Criteria: * Histologically or cytologically documented locally advanced or metastatic solid tumor malignancy. * Adequate bone marrow, kidney and liver function * Performance status of 0 or 1. * Resolved acute effects of any prior therapy to baseline severity or CTCAE Grade 1 except for AEs not constituting a safety risk by Investigator judgement. Exclusion Criteria: * Prior treatment targeting ILT3. * Prior treatment targeting LAIR1.

Study Info

Organization

NGM Biopharmaceuticals, Inc


Primary Outcome

Number of Patients with Dose-limiting Toxicities


Outcome Timeframe Baseline up to 21 Days

NCTID NCT05215574

Phases PHASE1

Primary Purpose TREATMENT

Start Date 2022-03-31

Completion Date 2025-07

Enrollment Target 130

Interventions

DRUG NGM831

DRUG NGM831 plus pembrolizumab (KEYTRUDA®)

DRUG NGM831 and NGM438 plus pembrolizumab (KEYTRUDA®)

Locations Recruiting

NGM Clinical Study Site

United States, Arizona, Gilbert


NGM Clinical Study Site

United States, California, Los Angeles


NGM Clinical Study Site

United States, Florida, Sarasota


NGM Clinical Study Site

United States, Florida, Tampa


NGM Clinical Study Site

United States, Michigan, Grand Rapids


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