Education and Training
Study of Magrolimab Combination Therapy in Patients With Head and Neck Squamous Cell Carcinoma
The goals of this clinical study are to learn about the safety, tolerability, dosing and effectiveness of the study drug, magrolimab in combination with other anticancer therapies in patients with head and neck squamous cell carcinoma (HNSCC).
Stanford is currently not accepting patients for this trial.
Stanford Investigator(s):
Intervention(s):
- drug: Magrolimab
- drug: Pembrolizumab
- drug: Docetaxel
- drug: 5-FU
- drug: Cisplatin
- drug: Carboplatin
- drug: Zimberelimab
Eligibility
Key Inclusion Criteria:
- Histologically or cytologically confirmed metastatic or locally recurrent HNSCC that
is considered incurable by local therapies.
Safety Run-in Cohort 1 and Phase 2 Cohorts 1
- Should not have had prior systemic therapy administered in the recurrent or metastatic
setting.
- Eligible primary tumor locations include oropharynx, oral cavity, hypopharynx, and
larynx. Nasopharynx is not included.
- HNSCC per protocol specified inclusion criteria regardless of PD-L1 status.
Safety Run-in Cohort 2 and Phase 2 Cohort 3
- Histologically or cytologically confirmed locally advanced/mHNSCC regardless of PD-L1
status with at least 1 and no more than 2 lines of prior systemic anticancer therapy
in the locally advanced/metastatic setting.
Key Exclusion Criteria:
- Active central nervous system (CNS) disease (individuals with asymptomatic and stable,
treated CNS lesions who have been off corticosteroids, radiation, or other
CNS-directed therapy for at least 4 weeks are not considered active).
- History of (noninfectious) pneumonitis that required steroids or current pneumonitis.
- Progressive disease within 6 months of completion of curatively intended treatment for
locally advanced/mHNSCC.
Safety Run-in Cohort 1, Pre-expansion Safety Run-in Cohort for Magrolimab + Pembrolizumab
(if Applicable), and Phase 2 Cohorts 1 and 2
- Prior treatment with any of the following:
- Anti-programmed cell death protein 1 or anti-PD-L1 checkpoint inhibitors.
- Anti-cytotoxic T-lymphocyte-associated protein 4 checkpoint inhibitors.
Safety Run-in Cohort 2 and Phase 2 Cohort 3
- Prior treatment with a taxane.
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Ages Eligible for Study
18 Years - N/A
Genders Eligible for Study
All
Not currently accepting new patients for this trial
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Elizabeth Winters
650-721-6509
Not Recruiting