Neovii Pharmaceuticals AG
5 News & Press Releases found

Neovii Pharmaceuticals AG news

Neovii Pharmaceuticals AG (“Neovii”), a Swiss based global specialty-care biopharmaceutical company, and Shanghai Fosun Pharmaceutical Industry Development Co. Ltd (“Fosun Pharma Industry”), a subsidiary of Shanghai Fosun Pharmaceutical (Group) Co., Ltd. (“Fosun Pharma”, Stock Code: 600196.SH, 02196.HK), a global pharmaceutical and healthcare industry group deep-rooted in China, have entered into an exclusive agreement (the “Agreement”), under w

Sep. 7, 2022

Dr. Christian Loss (57), former managing director of Neovii Biotech GmbH, Gräfelfing, is moving to the Swiss headquarters of Neovii Pharmaceuticals AG in Rapperswil as chief executive officer (CEO). As the new CEO in Germany, he will be succeeded by the former Neovii Head of Production, Sebastian Hofmann (40). With the change in management, two long-serving and experienced employees remain with the company: each have been with the company for more than ten years. Their joint mission is t

Oct. 26, 2021

RamotTel Aviv University’s technology transfer company, and Neovii, a Swiss-based biopharmaceutical company and a member of Israel-based Neopharm Group, announced today that they have signed a research and license agreement to develop a novel and potentially life-saving COVID-19 vaccine. Neovii will work in close collaboration with a team of scientists led by Prof. Jonathan Gershoni of 

May. 12, 2020

At the request of Neovii Biotech GmbH, the European Commission withdrew the marketing authorisation for Removab® (catumaxomab) in the European Union (EU).

Removab® was granted marketing authorisation in the EU on 20 April 2009 for treatment of malignant ascites in adults with EpCAM-positive carcinomas where standard therapy is not available or no longer feasible.

Since 2014, Removab could not be marketed due to the insolvency of the manufacturer of the drug substance.

Jul. 25, 2017

Neovii is pleased to announce the publication of the long-term outcomes of a multicenter parallel-group randomized trial conducted in Europe and Israel. The study looked at patients after standard GvHD prophylaxis with cyclosporine A and methotrexate with or without Grafalon® (anti-human-T-lymphocyte immunoglobulin- ATLG) (60 mg/kg total dose) in adult patients receiving myeloablative conditioning prior to hematopoietic stem cell transplantation from matched unrelated donors. Published in

Jun. 7, 2017