PMV Pharmaceuticals
PMVPPhase 1PMV Pharmaceuticals is a clinical-stage biopharmaceutical company focused on developing novel, small molecule therapies that selectively target p53 mutations, which are among the most common genetic drivers of cancer. The company's lead program, PC14586, is a first-in-class p53 Y220C reactivator currently in Phase 1/2 clinical trials. PMV's strategy centers on creating tumor-agnostic treatments that address specific p53 mutations, aiming to transform cancer care by targeting a fundamental oncogenic mechanism across multiple tumor types.
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AI Company Overview
PMV Pharmaceuticals is a clinical-stage biopharmaceutical company focused on developing novel, small molecule therapies that selectively target p53 mutations, which are among the most common genetic drivers of cancer. The company's lead program, PC14586, is a first-in-class p53 Y220C reactivator currently in Phase 1/2 clinical trials. PMV's strategy centers on creating tumor-agnostic treatments that address specific p53 mutations, aiming to transform cancer care by targeting a fundamental oncogenic mechanism across multiple tumor types.
Technology Platform
Proprietary platform for discovering small molecule p53 reactivators that selectively target specific p53 mutations through structural biology, fragment-based screening, and medicinal chemistry optimization.
Pipeline Snapshot
66 drugs in pipeline
| Drug | Indication | Stage |
|---|---|---|
| PC14586 + Itraconazole | Healthy Volunteers | Phase 1 |
| [14C]-PC14586 | Healthy Male Volunteers | Phase 1 |
| Azacitidine + Rezatapopt | Myelodysplastic Syndrome | Phase 1 |
| PC14586 + Rabeprazole + Famotidine | Healthy Volunteers | Phase 1 |
| metformin hydrochloride 500 mg tablet + rosuvastatin 10 mg tablet + repaglinide ... | TP53 Y220C Mutation | Phase 1 |
Funding History
3Total raised: $245M
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Competitive Landscape
PMV competes in the emerging p53-targeted therapy space against approaches like APR-246 (Aprea Therapeutics), MDM2 inhibitors, and gene therapies. The company's differentiation lies in its mutation-specific, structural biology-driven approach targeting precise p53 pockets, potentially offering greater selectivity than broader p53 reactivators.
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