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

Last updated: March 28, 2024
Sponsor: NGM Biopharmaceuticals, Inc
Overall Status: Active - Not Recruiting

Phase

1

Condition

Prostate Cancer

Esophageal Cancer

Cancer

Treatment

Pembrolizumab (KEYTRUDA ®)

NGM438

Clinical Study ID

NCT05311618
438-IO-101
MK-3475-E20
KEYNOTE-E20
  • Ages > 18
  • All Genders

Study Summary

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

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Histologically or cytologically documented locally advanced or metastatic solid tumormalignancy.
  • Progressed or was intolerant to all available therapies known to confer clinicalbenefit appropriate for their tumor type for which the patient was eligible andwilling to receive.
  • 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 1except for AEs not constituting a safety risk by Investigator judgement.

Exclusion

Exclusion Criteria:

• Prior treatment targeting LAIR1

Study Design

Total Participants: 71
Treatment Group(s): 2
Primary Treatment: Pembrolizumab (KEYTRUDA ®)
Phase: 1
Study Start date:
May 11, 2022
Estimated Completion Date:
June 30, 2025

Connect with a study center

  • SCRI Denver

    Denver, Colorado 80218
    United States

    Site Not Available

  • Yale Cancer Center

    New Haven, Connecticut 06520
    United States

    Site Not Available

  • Henry Ford Health System

    Detroit, Michigan 48202
    United States

    Site Not Available

  • START Midwest

    Grand Rapids, Michigan 49546
    United States

    Site Not Available

  • Mount Sinai Hospital

    New York, New York 10029
    United States

    Site Not Available

  • MD Anderson

    Houston, Texas 77030
    United States

    Site Not Available

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