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Clinical Trials in the UK / NCT06082167
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 UK tracker
Sponsor
Exelixis
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)

ZanzalintinibZanzalintinib-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)

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 the UK