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| Therapy Name | PF-07257876 |
| Synonyms | |
| Therapy Description |
PF-07257876 is a bispecific antibody that targets CD47 and PD-L1 (CD274), which may lead to increased phagocytosis and enhanced cytotoxic T-lymphocyte (CTL) response against tumor cells expressing CD47 and PD-L1 (CD274) (NCI Thesaurus). |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| PF-07257876 | PF 07257876|PF07257876 | CD47 Antibody 31 PD-L1 Inhibitor 15 | PF-07257876 is a bispecific antibody that targets CD47 and PD-L1 (CD274), which may lead to increased phagocytosis and enhanced cytotoxic T-lymphocyte (CTL) response against tumor cells expressing CD47 and PD-L1 (CD274) (NCI Thesaurus). |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|---|---|---|---|---|---|---|
| CD274 positive | Advanced Solid Tumor | predicted - sensitive | PF-07257876 | Phase I | Actionable | In a Phase I trial, PF-07257876 treatment was well tolerated in patients with PD-L1 (CD274)-positive advanced solid tumors and resulted in an objective response rate of 5.6% (1/18, 1 partial response in a patient with head and neck squamous cell carcinoma) (J Clin Oncol 41, 2023 (suppl 16; abstr 2529); NCT04881045). | detail... |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
|---|---|---|---|---|---|---|
| NCT04881045 | Phase I | PF-07257876 | Study to Test the Safety and Tolerability of PF-07257876 in Participants With Selected Advanced Tumors. | Completed | USA | ESP | 0 |