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Tyra Biosciences Initiates SURF301 Phase 1/2 Clinical Study and Doses First Patient with TYRA-300 - Vimarsana News

Tyra Biosciences Initiates SURF301 Phase 1/2 Clinical Study and Doses First Patient with TYRA-300

-TYRA-300 is the first oral, FGFR3-selective agent to be evaluated in the clinic- -Conference call and webcast today, Nov. 29th, at 9:00 am ET- CARLSBAD, Calif., Nov. 29, 2022 /PRNewswire/ -- Tyra...

Enfortumab Vedotin Plus Pembrolizumab 'Promising' for Untreated Advanced Urothelial Carcinoma - Vimarsana News

Enfortumab Vedotin Plus Pembrolizumab 'Promising' for Untreated Advanced Urothelial Carcinoma

Enfortumab vedotin plus pembrolizumab for advanced urothelial carcinoma may provide disease control with manageable safety.

Enfortumab Vedotin Plus Pembrolizumab 'Promising' for Untreated Advanced Urothelial Carcinoma - Vimarsana News

Enfortumab Vedotin Plus Pembrolizumab 'Promising' for Untreated Advanced Urothelial Carcinoma

Enfortumab vedotin plus pembrolizumab for advanced urothelial carcinoma may provide disease control with manageable safety.

Non-Chemo Regimen Led to High Response Rates in Cisplatin-Ineligible Bladder Cancer - Vimarsana News

Non-Chemo Regimen Led to High Response Rates in Cisplatin-Ineligible Bladder Cancer

'Encouraging activity' with enfortumab vedotin-pembrolizumab in patients with high unmet need

Seagen, Astellas and Merck Announce Results of Clinical Trial Investigating PADCEV® (enfortumab vedo - Vimarsana News

Seagen, Astellas and Merck Announce Results of Clinical Trial Investigating PADCEV® (enfortumab vedo

– Results demonstrated a 64.5% confirmed objective response rate in patients treated with investigational combination of enfortumab vedotin and pembrolizumab –– Data highlighted in late-breaking presentation at the European Society for Medical Oncology (ESMO) Congress 2022 –BOTHELL, Wash. & TOKYO & RAHWAY, N.J.--(BU...