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Nivolumab 240 mg / Relatlimab 80 mg in a fixed dose combination

Phase 2
Bristol-Myers Squibb Company (BMY)

Phase 2

Development Phase

0

Upcoming Catalysts

0

Historical Events

0

Regulatory Approvals

No Catalysts Found

No catalyst events have been recorded for this drug yet.

Competitive Landscape

0 competitors in Cutaneous Squamous Cell Carcinoma

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Drug Information

Target Indication

Cutaneous Squamous Cell Carcinoma

Clinical Trial

NCT06288191

Last updated: 10/2/2026

Patent & Exclusivity

No patent data available. Pre-approval drugs may not have Orange Book listings.

Drug Science
Mechanism of action & safety profile
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