CASTELVECCHIO PASCOLI, Italy, July 1, 2024 /PRNewswire/ -- Kedrion Biopharma Inc. announced today that it has established the framework for a long-term agreement with Biotest AG for the full commercialization and distribution of the immunoglobulin therapy Yimmugo® in the U.S., following its Biologic License Application (BLA) approval by the U.S. Food and Drug Administration (FDA) on June 13, 2024.
FORT LEE, N.J., April 29, 2024 /PRNewswire/ -- Kedrion Biopharma Inc., an international biopharmaceutical company specializing in the research and development, production, and commercialization of plasma-derived therapeutic products used in treating rare and serious diseases, announced today that plasminogen deficiency type 1 (PLGD-1) patients in the U.S. now have access to RYPLAZIM® (plasminogen, human-tvmh).
CASTELVECCHIO PASCOLI, Italy, Dec. 7, 2023 /PRNewswire/ -- Kedrion Biopharma, a leading global biopharmaceutical company that develops, manufactures and commercializes therapeutic products derived from blood plasma, announces the execution of a binding memorandum of understanding with Kamada Ltd. (NASDAQ: KMDA; TASE: KMDA.TA), an Israeli commercial stage global biopharmaceutical company and leader in the specialty plasma-derived field, for the amendment and the 8-year extension of the KEDRAB® US distribution agreement between the two companies.
FORT LEE, N.J., July 25, 2023 /PRNewswire/ -- Kedrion Biopharma, an international biopharmaceutical company specializing in the production and distribution of plasma-derived therapeutic products used in treating rare and serious diseases recently announced its support of the Immune Deficiency Foundation (IDF) Research Grant Program for the second year in a row. Bioproducts Laboratory (BPL), a UK-based company with over 60 years of experience in the supply of high-quality plasma-derived medicines for the treatment of rare diseases, first provided the grant in 2022. That same year, Kedrion joined forces with BPL to form the new Kedrion.
FORT LEE, N.J., July 12, 2023 /PRNewswire/ -- Kedrion Biopharma, an international biopharmaceutical company specializing in the production and distribution of plasma-derived therapeutic products used in treating rare and serious diseases, has announced that China's National Institutes for Food and Drug Control (NIFDC) has approved BPL's human Albumin product for release to the Chinese market. In 2022, Kedrion joined forces with BPL, a UK-based company with over 60 years of experience in the supply of high-quality plasma-derived medicines for the treatment of rare diseases.
Kedrion strengthens its network of plasma collection centers
(Castelvecchio Pascoli, Lucca) April 29, 2022 – Kedrion Biopharma, the Italian biopharmaceuticals group, has redeemed €200m euros of its notes that...
The Board of Directors of Kedrion S.p.A., a biopharmaceutical company that specializes in the development, production and distribution of...
LES ULIS, France and LUCCA, Italy, Jan. 31, 2022 /PRNewswire/ -- Two leading European pharmaceutical companies, LFB and Kedrion, are joining forces in an industrial cooperation agreement to increase the availability of immunoglobulin, a plasma-derived medicine, for patients in France.
FORT LEE, N.J., Oct. 20, 2021 /PRNewswire/ -- Kedrion Biopharma, an international biopharmaceutical company specialized in the manufacture and distribution of plasma-derived therapeutic products used in treating rare and serious diseases, is now gearing up to commercialize and distribute RYPLAZIM® (plasminogen human-tvmh) in the United States. RYPLAZIM is indicated to treat plasminogen deficiency type 1, also known as C-PLGD, an ultra-rare condition affecting less than 2,000 people in the U.S.