Opevesostat
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Other names | MK-5684, ODM-208 |
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Formula | C21H26N2O5S |
Molar mass | 418.51 g·mol−1 |
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Opevesostat is an investigational new drug being developed for the treatment of metastatic castration-resistant prostate cancer (mCRPC).[1] It is a non-steroidal, selective inhibitor of CYP11A1 (cholesterol side-chain cleavage enzyme)[2] discovered by Orion Corporation and currently undergoing clinical development by Merck & Co., Inc. Opevesostat's mechanism of action involves suppressing the production of steroid hormones and their precursors that may activate the androgen receptor signaling pathway, which is crucial in prostate cancer progression. As of 2024, opevesostat is being evaluated in two Phase 3 clinical trials, OMAHA1 and OMAHA2a, which are assessing its efficacy and safety in combination with hormone replacement therapy for patients with mCRPC who have failed prior treatments.[3][4][5]
References
[edit]- ^ "Opevesostat - Orion". AdisInsight.
- ^ Kim C, Jeong E, Lee YB, Kim D (July 2024). "Steroidogenic cytochrome P450 enzymes as drug target". Toxicological Research. 40 (3): 325–333. doi:10.1007/s43188-024-00237-0. PMID 38911541.
- ^ "Merck and Orion Announce Mutual Exercise of Option Providing Merck Global Exclusive Rights to Opevesostat". StockTitan. Retrieved 2024-11-23.
- ^ "Inside Information: Orion and MSD Announce Mutual Exercise of Option Providing MSD Global Exclusive Rights to Opevesostat". Orion. Retrieved 2024-11-23.
- ^ "Merck and Orion Announce Mutual Exercise of Option Providing Merck Global Exclusive Rights to Opevesostat". Merck. Retrieved 2024-11-23.