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Clinical Trial Active — Not Recruiting Phase II / Phase III NCT06295731

INBRX-106 in Combination With Pembrolizumab in First-line PD-L1 CPS≥20 HNSCC

INBRX-106 in Combination With Pembrolizumab in First-line PD-L1 CPS≥20 HNSCC — Active Not Recruiting • Phase II / Phase III • Oncology • NCT06295731.

📅 31 Mar 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase II / Phase III
NCT ID
NCT06295731
Start
2024-05-14
Completion
2029-05
ClinicaliQ Trial Snapshot
  • INBRX-106 in Combination With Pembrolizumab in First-line PD-L1 CPS≥20 HNSCC — Active Not Recruiting • Phase II / Phase III • Oncology • NCT06295731.
  • Review the linked registry entry for study design, population, endpoints, and operational status.

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What This Trial Is Studying

This seamless phase 2/3 randomized controlled study will evaluate the efficacy and safety of the hexavalent OX40 agonist antibody INBRX-106 combined with the anti-PD-1 antibody pembrolizumab versus pembrolizumab (+ placebo in phase 3) as first-line treatment for patients with locally advanced recurrent or metastatic head and neck squamous cell carcinoma (R/M HSNSCC) incurable by local therapies, expressing PD-L1 with a combined proportion score (CPS) ≥20. Conditions: Head and Neck Squamous Cell Carcinoma (HNSCC) Interventions: INBRX-106, Pembrolizumab Lead Sponsor: Inhibrx Biosciences, Inc Planned Enrollment: 410 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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