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Active, not recruiting Phase 2/3

Study of Zanzalintinib (XL092) + Pembrolizumab vs Pembrolizumab in Subjects With PD-L1 Positive Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

NCT06082167 · tracked via the Priya Life Science Poland tracker
Sponsor
Phase
Phase 2/3
Started
2024-06-07
Last updated
2025-08-17

Condition(s) studied

Head and Neck Squamous Cell Carcinoma

Investigational drug(s) / intervention(s)

Zanzalintinib →Zanzalintinib-matched PlaceboPembrolizumab →

Zanzalintinib: Specified doses on specified days

Zanzalintinib-matched Placebo: Specified doses on specified days

Pembrolizumab: Specified doses on specified days

Study summary

This is a multicenter, randomized, double-blind, controlled Phase 2/3 trial of zanzalintinib in combination with pembrolizumab versus zanzalintinib-matched placebo in combination with pembrolizumab in subjects with programmed death-ligand 1 (PD-L1) positive recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) incurable by local therapies who have not received prior systemic therapy for recurrent or metastatic disease.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Histologically or cytologically-confirmed R/M HNSCC that is considered incurable by local therapy. * Should not have had prior systemic therapy administered in the recurrent or metastatic setting. Systemic therapy which was completed more than 6 months prior to randomization if given as part of multimodal treatment for locally advanced disease is allowed. * The eligible primary tumor locations are the oropharynx, oral cavity, hypopharynx, and larynx. * PD-L1 expression level Combined Positive Score (CPS) ≥ 1. * Participants with oropharyngeal cancer must have human papillomavirus (HPV) status from tumor tissue. * Measurable disease according to RECIST 1.1 as determined by the Investigator. * Tumor samples (archival or fresh tumor biopsy) are required. If archival tissue is unavailable, must provide fresh tumor tissue biopsy prior to randomization. * Recovery to baseline or ≤ Grade 1 severity (CTCAE v5) from adverse events (AEs) related to any prior treatments, unless AE(s) are clinically nonsignificant and/or stable on supportive therapy. * Age 18 years (or the legal age of consent in your country, if higher than 18) or older on the day of consent. * Eastern Cooperative Oncology Group (ECOG) performance status of 0-1. * Adequate organ and marrow function. Exclusion Criteria: * Nasopharynx, salivary gland or occult primary site (regardless of p16 status). * Has disease that is suitable for local therapy administered with curative intent. * Has received prior therapy with zanzalintinib, any anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (for example, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), OX-40, CD137). * Life expectancy \< 3 months. * Had progressive disease within 6 months of completion of curatively intended systemic treatment for locoregionally advanced HNSCC. * Radiation therapy for bone metastases within 2 weeks, any other radiation therapy within 4 weeks prior to randomization. * Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery (including radiosurgery) and stable for at least 4 weeks prior to randomization. * Positive hepatitis B surface antigen (HBsAg) test. * Positive hepatitis C virus (HCV) antibody test. * Major surgery (eg, GI surgery, removal or biopsy of brain metastasis) within 8 weeks prior to randomization. Complete wound healing from major or minor surgery must have occurred at least prior to randomization. * Corrected QT interval calculated by the Fridericia formula (QTcF) \> 480 ms per electrocardiogram (ECG) within 28 days before randomization. * Pregnant or lactating females. * Administration of a live, attenuated vaccine within 30 days before randomization.

Primary outcome measure(s)

  • Progression-Free Survival (PFS) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) by Blinded Independent Central Review (BICR) — Approximately 33 months after the first subject is randomized
    Defined as the time from randomization to the earlier of either radiographic progressive disease (PD) per RECIST 1.1 as determined by the BICR or death from any cause
  • Overall Survival (OS) — Approximately 50 months after the first subject is randomized
    Defined as the time from randomization to death due to any cause

Trial sites (168)

FacilityCityRegionStatus
Exelixis Clinical Site #2 Fullerton California
Exelixis Clinical Site #1 Orange City Florida
Exelixis Clinical Site #163 Tampa Florida
Exelixis Clinical Site #123 Athens Georgia
Exelixis Clinical Site #82 Atlanta Georgia
Exelixis Clinical Site #19 Chicago Illinois
Exelixis Clinical Site #62 Des Moines Iowa
Exelixis Clinical Site #100 Iowa City Iowa
Exelixis Clinical Site #4 St Louis Missouri
Exelixis Clinical Site #148 Lebanon New Hampshire
Exelixis Clinical Site #158 Camden New Jersey
Exelixis Clinical Site #3 Shirley New York
Exelixis Clinical Site #95 Durham North Carolina
Exelixis Clinical Site #117 Wilson North Carolina
Exelixis Clinical Site #43 Roanoke Virginia
Exelixis Clinical Site #73 Rosario Santa Fe Province
Exelixis Clinical Site #91 Buenos Aires Argentina
Exelixis Clinical Site # 47 Ciudad Autonoma de Buenos Aire Argentina
Exelixis Clinical Site #53 Ciudad Autonoma de Buenos Aire Argentina
Exelixis Clinical Site #93 Córdoba Argentina
Exelixis Clinical Site #64 Córdoba Argentina
Exelixis Clinical Site #157 Pergamino Argentina
Exelixis Clinical Site #92 Santa Fe Argentina
Exelixis Clinical Site #57 Port Macquarie New South Wales
Exelixis Clinical Site # 46 Adelaide Australia
Exelixis Clinical Site #154 Bedford Park Australia
Exelixis Clinical Site #137 Camperdown Australia
Exelixis Clinical Site #39 Murdoch Australia
Exelixis Clinical Site #156 Linz Austria
Exelixis Clinical Site #42 Salzburg Austria
Exelixis Clinical Site #166 Vienna Austria
Exelixis Clinical Site #22 Brussels Belgium
Exelixis Clinical Site #106 Charleroi Belgium
Exelixis Clinical Site #14 Libramont Belgium
Exelixis Clinical Site #37 Sint-Niklaas Belgium
Exelixis Clinical Site #68 Passo Fundo Rio Grande do Sul
Exelixis Clinical Site #90 Porto Alegre Rio Grande do Sul
Exelixis Clinical Site #110 Jaú São Paulo
Exelixis Clinical Site #65 Santo André São Paulo
Exelixis Clinical Site #83 São José do Rio Preto São Paulo

+ 128 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06082167 on ClinicalTrials.gov ↗ ← All trials in Poland