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