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A Phase 1/2 Dose Escalation/Expansion Study of NGM707 As Monotherapy and in Combination with Pembrolizumab in Advanced or Metastatic Solid Tumor Malignancies
Study of NGM707 as Monotherapy and in Combination with Pembrolizumab in Advanced or Metastatic Solid Tumor Malignancies
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
NGM Clinical Study Site
Los Angeles, California, United States
NGM Clinical Study Site
Newport Beach, California, United States
NGM Clinical Study Site
Santa Monica, California, United States
NGM Clinical Study Site
Santa Rosa, California, United States
NGM Clinical Study Site
Lone Tree, Colorado, United States
NGM Clinical Study Site
Washington D.C., District of Columbia, United States
NGM Clinical Study Site
Sarasota, Florida, United States
NGM Clinical Study Site
Baltimore, Maryland, United States
NGM Clinical Study Site
Boston, Massachusetts, United States
NGM Clinical Study Site
Grand Rapids, Michigan, United States
Start Date
June 9, 2021
Primary Completion Date
February 1, 2025
Completion Date
July 1, 2025
Last Updated
October 2, 2024
179
ESTIMATED participants
NGM707
DRUG
NGM707 plus pembrolizumab (KEYTRUDA®)
DRUG
NGM707 plus pembrolizumab (KEYTRUDA®)
DRUG
NGM707 plus pembrolizumab (KEYTRUDA®)
DRUG
NGM707 plus pembrolizumab (KEYTRUDA®)
DRUG
NGM707
DRUG
NGM707
DRUG
NGM707
DRUG
Lead Sponsor
NGM Biopharmaceuticals, Inc
Collaborators
NCT07485114
NCT00083512
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05839379