August 16, 2024 16:05 ET ROCKVILLE, Md., Aug. 16, 2024 (GLOBE NEWSWIRE) — Theriva Biologics, Inc. (NYSE American: TOVX), a diversified clinical-stage company developing therapeutics designed to treat diseases in areas of high unmet need, announced today a reverse stock split of its issued and outstanding common stock, par value $0.001 per share, at a […]
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August 13, 2024 08:00 ET – VIRAGE, the Phase 2b clinical trial of VCN-01 in combination with chemotherapy for metastatic Pancreatic Ductal Adenocarcinoma (PDAC), is expected to complete enrollment in the third quarter of 2024- – Received Fast Track Designation (FTD) Granted by the U.S. Food and Drug Administration (FDA) for VCN-01 for the treatment
August 13, 2024 15:09 ET – Se espera que la inscripción a VIRAGE, el ensayo clínico de Fase 2b de VCN-01 en combinación con quimioterapia para el adenocarcinoma pancreático ductal metastásico (PDAC), finalice en el tercer trimestre de 2024 – – Obtención de la designación de vía rápida (FTD) concedida por la Administración de Alimentos
July 31, 2024 08:15 ET ROCKVILLE, Md., July 31, 2024 (GLOBE NEWSWIRE) — Theriva™ Biologics, Inc. (NYSE American: TOVX), a diversified clinical-stage company developing therapeutics designed to treat cancer and related diseases in areas of high unmet need, today announced that the U.S. Food and Drug Administration (FDA) granted Rare Pediatric Drug Designation (RPDD) for
July 31, 2024 17:32 ET ROCKVILLE, Maryland, July 31, 2024 (GLOBE NEWSWIRE) — Theriva™ Biologics, Inc. (NYSE American: TOVX), una empresa diversificada de fase clínica que desarrolla terapias diseñadas para tratar el cáncer y enfermedades relacionadas en áreas de gran carencia, ha anunciado hoy que la Administración de Alimentos y Medicamentos (FDA, por sus siglas
May 23, 2024 21:38 ET ROCKVILLE, Maryland, May 24, 2024 (GLOBE NEWSWIRE) — Theriva™ Biologics (NYSE American: TOVX), una empresa diversificada de fase clínica que desarrolla terapias diseñadas para tratar el cáncer y enfermedades relacionadas en áreas de gran carencia, ha anunciado hoy que la Administración de Alimentos y Medicamentos de los Estados Unidos (FDA)
May 23, 2024 08:15 ET ROCKVILLE, Md., May 23, 2024 (GLOBE NEWSWIRE) — Theriva™ Biologics (NYSE American: TOVX), a diversified clinical-stage company developing therapeutics designed to treat cancer and related diseases in areas of high unmet need, today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track Designation (FTD) to lead
May 08, 2024 06:39 ET – Se han presentado datos de primera línea del ensayo de fase 1 patrocinado por investigadores del VCN-01 por vía intravítrea en pacientes pediátricos con retinoblastoma refractario; el comité de vigilancia del estudio dictaminó que los resultados del ensayo son positivos – – Se han presentado datos preclínicos que demuestran
May 07, 2024 07:00 ET – Reported topline data from the investigator sponsored Phase 1 trial of intravitreal VCN-01 in pediatric patients with refractory retinoblastoma; trial results were determined to be positive by the study Monitoring Committee- -Presented preclinical data demonstrating the potential synergy between VCN-01 and liposomal irinotecan in a human pancreatic mouse xenograft
April 23, 2024 07:00 ET –Phase 1 trial in collaboration with Sant Joan de Déu-Barcelona Children’s Hospital (SJD) determined to have a positive outcome by the study Monitoring Committee– –Safety and clinical outcomes support the therapeutic potential of VCN-01 in retinoblastoma and emphasize VCN-01’s potential for use in diverse cancer indications– ROCKVILLE, Md., April 23,
