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Aravive Announces First Patient Dosed in Phase 3 Registrational Trial Evaluating AVB-500 in Patients with Platinum Resistant Ovarian Cancer

Share: U.S. FDA Granted Fast Track Designation in 2018 Trial Expected to Enroll 300-400 Patients at Approximately 165 Sites in the U.S. and Europe in Simplified Adaptive Trial Design Conference Call and Webcast Today at 8:30 a.m. ET HOUSTON, April 27, 2021 (GLOBE NEWSWIRE) Aravive Inc. (NASDAQ:ARAV), a clinical-stage oncology company developing innovative therapeutics to treat life-threatening diseases, today announced the Company has dosed the first patient in its Phase 3 trial of AVB-500 in platinum resistant ovarian cancer (PROC). The trial is evaluating the efficacy of AVB-500 in combination with paclitaxel (chemotherapy) and the primary endpoint is progression free survival.

Journal of Lower Genital Tract Disease publishes a clinical trial endorsing PAPILOCARE as a proven treatment that prevents and treats lesions caused by HPV

Journal of Lower Genital Tract Disease publishes a clinical trial endorsing PAPILOCARE as a proven treatment that prevents and treats lesions caused by HPV of patients affected by high-risk HPV The Paloma Clinical trial also certifies a clearance of HPV in 63% of patients with high-risk HPV treated with PAPILOCARE compared with 40% in the control group. MADRID, Spain, April 7, 2021 /PRNewswire/ The Journal of Lower Genital Tract Disease (JLGTD), the official journal of the American Society for Colposcopy and Cervical Pathology (ASCCP), have published the final results of the Paloma Clinical Trial, which demonstrated the efficacy of PAPILOCARE in preventing and treating lesions caused by HPV. Its main conclusions include the

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