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Search / Trial NCT03743766

Nivolumab, BMS-936558 in Combination with Relatlimab, BMS-986016 in Patients with Metastatic Melanoma Naïve to Prior Immunotherapy in the Metastatic Setting

Launched by JOHN KIRKWOOD · Nov 15, 2018

Trial Information

Current as of May 20, 2025

Completed

Keywords

Stage Iiib Stage Iiic Stage Iiid Stage Iv Immune Checkpoint Blockade (Icb) Lymphocyte Activation Gene 3 (Lag3; Cd223) Immunotherapy

ClinConnect Summary

This study will evaluate the antitumor activity of anti-LAG3 monoclonal antibody relatlimab and the anti-PD1 monoclonal antibody nivolumab in combination in subjects with unresectable or metastatic melanoma who have not received prior treatment with immunotherapy. The trial is designed with a lead-in phase of 2 cycles (4 week) treatment of either nivolumab, relatlimab, or the combination of nivolumab/relatlimab, followed by a combination phase of nivolumab/relatlimab treatment in all subjects. This lead-in design with accompanying tumor biopsies and peripheral blood analyses will enable mec...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • • Men or women 18 years of age or older meeting AJCC 8th edition criteria for unresectable stage IIIB, stage IIIC, stage IIID, or stage IV melanoma who have not received treatment with immunotherapy in the metastatic setting
  • Exclusion Criteria:
  • * Known or suspected CNS metastases, with the following exceptions:
  • Subjects with controlled brain metastases will be allowed to enroll. Controlled brain metastases are defined as no radiographic progression for at least 4 weeks following radiation and/or surgical treatment at the time of consent. Subjects must be off steroids for at least 2 weeks prior to randomization.
  • Subjects with signs or symptoms of brain metastases are not eligible unless brain metastases are ruled out by computed tomography or magnetic resonance imaging.
  • Active autoimmune disease requiring treatment, with the exception of type 1 diabetes mellitus, vitiligo, resolved childhood asthma/atopy, controlled hyper/hypothyroidism, hypoadrenalism or hypopituitarism.
  • Prior systemic treatment in the metastatic setting, including anti-PD1, anti-PDL1, anti-PDL2, anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell costimulation or immune checkpoint pathways; or chemotherapy.
  • Prior adjuvant treatment with anti-PD1, anti-PDL1, and/or anti-LAG3 antibody. Note that prior adjuvant treatment with targeted therapy (e.g. BRAF/MEK inhibition), anti-CTLA4, or treatment not otherwise specified above would be permitted.
  • Ocular melanoma

About John Kirkwood

John Kirkwood is a distinguished clinical trial sponsor renowned for its commitment to advancing medical research and improving patient care. With a focus on innovative therapies and rigorous scientific methodologies, the organization plays a pivotal role in the development of new treatments across various therapeutic areas. Leveraging a robust network of clinical investigators and state-of-the-art facilities, John Kirkwood emphasizes collaboration and integrity in its clinical trials, ensuring adherence to the highest ethical standards and regulatory compliance. Through its dedication to excellence, the organization strives to contribute significantly to the future of healthcare.

Locations

Pittsburgh, Pennsylvania, United States

Patients applied

0 patients applied

Trial Officials

John Kirkwood, MD

Principal Investigator

University of Pittsburgh

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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