An Investigational Immuno-therapy Study of BMS-986205 Combined With Nivolumab, Compared to Nivolumab by Itself, in Patients With Advanced Melanoma

• Status: Completed
• Trial end date: 2020-07-02
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to see if BMS-986205 combined with nivolumab, compared to nivolumab by itself, is more effective in treating Melanoma that has spread or is unable to be removed by surgery, and has not previously been treated

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Bristol-Myers Squibb
• Treatments: Linrodostat; Nivolumab

Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com

Inclusion Criteria:

• 12 years and older unless not permitted by local regulations; in that case 18 years old and older

• Eastern Cooperative Oncology Group (ECOG) performance status of less than or equal to 1

• Histologically confirmed Stage III (unresectable) or Stage IV melanoma, per the American Joint Committee on Cancer (AJCC) Staging Manual (8th edition)

• Treatment-naïve participants (no prior systemic anticancer therapy for unresectable or metastatic melanoma)

• Measurable disease per RECIST v1.1

Exclusion Criteria:

• Active brain metastases or leptomeningeal metastases

• Uveal or ocular melanoma

• Participants with active, known, or suspected autoimmune disease

• Prior malignancy active within the previous 3 years except for locally curable cancers that have been apparently cured

Other protocol defined inclusion/exclusion criteria could apply