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
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
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.