mAbxience | News

Boosting biologics and Contract Manufacturing at mAbxience facilities


CDMO and biosimilars maker mAbxience will install a new ABEC 4,000 L CSR Single use bioreactor at one of its site. mAbxience, a leading international biopharmaceutical company, with over a decade of experience in the development, manufacture and commercialization of biopharmaceuticals is set to continue its ambitious growth plans with the installation of a new […]

HK inno.N licenses in mAbxience’s denosumab biosimilar


HK inno.N said it has signed an exclusive license agreement with Spain’s mAbxience to market the latter’s Prolia (ingredient: denosumab) biosimilar, a preventive treatment for osteoporosis and cancer-related skeletal complications, in Korea. Under the contract, HK inno.N will exclusively market two types of denosumab biosimilars – 60 mg and 120 mg — from mAbxience, and […]

mAbxience II Biosimilar Forum


To drive scientific exchange on biopharmaceuticals and high-quality treatment options, more than 180 physicians, pharmacists, and hospital managers from around the world came together in a global conference and over 423 attendees via streaming. On October 21, mAbxience, a leading international biopharmaceutical company of which Fresenius Kabi acquired a majority stake, has celebrated its 2nd […]

Fresenius Kabi completes majority stake acquisition of mAbxience Holding S.L., significantly enhancing presence in high-growth biopharmaceuticals market


A further milestone for Fresenius Kabi’s Vision 2026 growth strategy as the company invests on the core growth vector “Broaden in Biopharma” The combination of both companies positions Fresenius Kabi for accelerated medium- and long-term growth building on a highly complementary product offering in one of the fastest-growing areas of healthcare Enables entry into high-growth […]

FDA Approves Alymsys® (bevacizumab-maly), a Biosimilar of Bevacizumab by Amneal Pharmaceuticals, Inc., developed by mAbxience


Amneal Pharmaceuticals, Inc. (NYSE: AMRX) (“Amneal” or the “Company”) announced that the U.S. Food and Drug Administration (FDA) has approved the Company’s Biologics License Application (BLA) for bevacizumab-maly, a biosimilar referencing Avastin®. The product will be marketed under the proprietary name ALYMSYS® and represents the third bevacizumab biosimilar approved in the U.S. ALYMSYS® was developed […]

Insud Pharma and Fresenius Kabi combine efforts to accelerate the growth of mAbxience


This agreement will bring new business to the biotech company, which is expanding its manufacturing capabilities and maintains its identity, brand, and complete team   The transaction validates mAbxience differentiated core competencies in the development, manufacturing and commercialization of biopharmaceutical products   With this strategic transaction the Spanish group Insud will also have resources to […]

Cipla enters partnership to provide affordable oncology biosimilars to South Africa


Cipla Medpro and the wholly owned subsidiary of Cipla Limited, India have finalised a partnership agreement with the global biotechnology company mAbxience, to get oncology and respiratory-related biosimilars to South Africa. These medicine products for the treatment of cancer are on the WHO Model List of Essential Medicines. The mAbxience partnership will enable Cipla to […]

Insud Pharma donation and assistance – Ukraine war situation


At Insud Pharma we are deeply concerned about the war situation in Ukraine, hoping for a fast, peaceful resolution as soon as possible. Our thoughts are with everyone affected by this war and with the people who are suffering and fearing for their lives and livelihood. From the beginning, we are in continuous contact with […]

mAbxience launches its CDMO platform to third parties


mAbxience, an experienced, specialized global biotechnology company, aims to leverage its capacity, expertise and proven track record in the optimization of biologic development & manufacturing programs for third parties. With a global mission to make biologic medicines accessible and affordable across the globe, mAbxience aims to focus its core expertise to accelerate and transform current […]

mAbxience’s biosimilar approved in Japan


Nichi-Iko Pharmaceutical Co., Ltd. has recently announced that it received approval for a biosimilar of bevacizumab BS intravenous infusion 100 mg/400 mg, whose marketing authorization application was filed based on the clinical pharmacokinetic (PK) study data conducted in Japan in addition to the global Phase 3 study data conducted by mAbxience. Bevacizumab BS is highly […]