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Evopoint doesn't follow Pfizer into prostate cancer
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The controversial space of EZH2 inhibition recently welcomed one highly prominent pivotal entrant, Pfizer, and it's about to see another. Evopoint Biosciences' EZH2 inhibitor XNW5004 will start its first phase 3 study next month, a new listing on the clinicaltrials.gov registry has revealed. However, this move is rather less contentious than Pfizer's, concerning the somewhat niche setting of peripheral T-cell lymphoma. For its part Pfizer put its EZH2 contender, mevrometostat, on the fast track in the high-profile space of castration-resistant prostate cancer, moving it from phase 1 straight into phase 3, and then started a second pivotal study in the first-line setting. Pfizer's rationale was that EZH2 can be seen in prostate cancer progression, and blocking EZH2 has preclinically been shown to reverse resistance to next-generation hormonal agents, but this has been thrown into doubt clinically by the failures of Novartis's MorphoSys-derived tulmimetostat and CPI-1205, and Ipsen's Tazverik. Evopoint has studied XNW5004 in prostate cancer in phase 2, but it's notable that it hasn't – yet – followed Pfizer by taking the molecule into pivotal development in this setting.
EZH2 inhibitors in phase 3
Project | Company | Phase 3 setting |
---|---|---|
Tazverik | Ipsen (ex Epizyme) | Approved for epithelioid sarcoma & follicular lymphoma |
Mevrometostat | Pfizer | Mevpro-1 in 2L mCRPC, Xtandi combo vs Xtandi/docetaxel; Mevpro-2 in 1L mCRPC, Xtandi combo vs Xtandi |
SHR2554 | Treeline Biosciences/ Jiangsu HengRui | ≥2L peripheral T-cell lymphoma, vs tucidinostat (HDAC inhibitor) |
XNW5004 | Evopoint Biosciences | ≥2L peripheral T-cell lymphoma, vs tucidinostat (HDAC inhibitor) |
Source: OncologyPipeline.
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