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About
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).
Enrollment
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Inclusion and exclusion criteria
Key Inclusion Criteria:
Safety Run-in Cohort 1 and Phase 2 Cohorts 1
Safety Run-in Cohort 2 and Phase 2 Cohort 3
Key Exclusion Criteria:
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:
Safety Run-in Cohort 2 and Phase 2 Cohort 3
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Primary purpose
Allocation
Interventional model
Masking
193 participants in 8 patient groups
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Central trial contact
Gilead Clinical Study Information Center
Data sourced from clinicaltrials.gov
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