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First Ascent Biomedical Presents Findings from Clinical Studies in Pediatric and Adult Cancers Using its AI-Enhanced Functional Precision Medicine Platform at ASCO 2024 - Vimarsana News

First Ascent Biomedical Presents Findings from Clinical Studies in Pediatric and Adult Cancers Using its AI-Enhanced Functional Precision Medicine Platform at ASCO 2024

MIAMI--(BUSINESS WIRE)--Jun 1, 2024--

Ocular Therapeutix™ Announces Positive Phase 2 PAXTRAVA™ - Vimarsana News

Ocular Therapeutix™ Announces Positive Phase 2 PAXTRAVA™

Phase 2 data highlight consistent and sustained reductions in Intraocular Pressure (IOP), statistically significant (p<0.0001) through six months, with...

U.S. Food and Drug Administration Approves ZELSUVMI&#x2122; as a First-in-Class Medication for the Treatment of Molluscum Contagiosum - Vimarsana News

U.S. Food and Drug Administration Approves ZELSUVMI&#x2122; as a First-in-Class Medication for the Treatment of Molluscum Contagiosum

ZELSUVMI™ is expected to be commercially available during the second half of 2024 ...

Propanc Biopharma Targets Site of First-In-Human Study for PRP at the Peter Mac Cancer Center, Melbourne, Australia - Vimarsana News

Propanc Biopharma Targets Site of First-In-Human Study for PRP at the Peter Mac Cancer Center, Melbourne, Australia

Initial Discussion Held with Clinical Investigator at Australia’s Biggest Cancer Hospital

SELLAS Announces Confirmatory Top-Line Data Showing Survival and Clinical Benefits Based on the Final Analysis of the Phase 1/2 Clinical Trial of Galinpepimut-S in Combination with Keytruda&#xAE; (pembrolizumab) in Patients with WT1+ Platinum-Resistant Advanced Ovarian Cancer - Vimarsana News

SELLAS Announces Confirmatory Top-Line Data Showing Survival and Clinical Benefits Based on the Final Analysis of the Phase 1/2 Clinical Trial of Galinpepimut-S in Combination with Keytruda&#xAE; (pembrolizumab) in Patients with WT1+ Platinum-Resistant Advanced Ovarian Cancer

- Median Overall Survival for GPS Combination was 18.4 Months Compared to 13.8 months in a Checkpoint Inhibitor Single Agent Study in a Similar Patient Population Treated with Checkpoint Inhibitor... | November 10, 2022