Biotechnology company BioSenic’s affiliate Medsenic has amended its licence agreement with Australia-based pharmaceutical company Phebra for the oral formulation of arsenic trioxide (OATO).
Mont-Saint-Guibert, Belgium, November 8, 2022, 7am CET – BIOSENIC (Euronext Brussels and Paris: BIOS), the company specialized in serious autoimmune /inflammatory diseases and cell repair, today announces an update on its systemic autoimmune disease platform, originally designed by Medsenic. The update follows the announcement of the merger between Bone Therapeutics and Medsenic, and the listing on Euronext Brussels and Paris.
STRASBOURG, France--(BUSINESS WIRE)--Medsenic, a clinical stage biopharmaceutical company focusing on the discovery and development of new indications and formulations of arsenic salts for the treatment of severe autoimmune diseases, announced today a new publication in Transplantation and Cellular Therapy, - the official Journal of ASTCT (American Society for Transplantation and Cellular Therapy) - that provides insights from its drug Arscimed®, a GMP intravenous formulation of arsenic trioxide, in patients with Chronic Graft Versus Host Disease (cGvHD).
A Phase III clinical trial has found that the combination of all-trans retinoic acid and arsenic trioxide is highly effective in children with standard- and high-risk acute promyelocytic leukaemia (APL).
Eugia Pharma’s Generics Arsenic Trioxide Receives Approvals In US
STRASBOURG, France--(BUSINESS WIRE)--Medsenic, a clinical-stage biopharmaceutical company specializing in the discovery and development of new indications and formulations of arsenic salts for the treatment of severe autoimmune diseases, today announced that it has received from the US Patent and Trademark Office (USPTO) with Arscimed®, a notice allowance for a patent which enhances in the United States the protection of its intravenous formulation of arsenic trioxide, particularly in SLE repair.
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Syros Pharmaceuticals (NASDAQ:SYRS), a leader in the development of medicines that control the expression of genes, today announced that the first patient has been dosed in the dose confirmation study of SY-2101, a novel oral form of arsenic trioxide (ATO). The trial will evaluate the pharmacokinetics (PK), safety, and tolerability of SY-2101 to confirm the optimal dose to advance into a planned Phase 3 clinical trial in newly diagnosed acute promyelocytic leukemia (APL) patients.
medac Gesellschaft für klinische Spezialpräparate mbH Arsenic trioxide medac Receives Approval in Europe
Medac GmbH`s Arsenictrioxide medac (ArsenicTrioxide) Receives Approval In Europe
At its June 2020 meeting, the human medicines committee of the European Medicines Agency (EMA’s CHMP) recommended that 11 new medicines be approved for use in the European Union (EU); one of these, Dapirivine Vaginal Ring, was recommended under EU Medicines for All, a mechanism for medicines that are also to be used outside the EU.