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The U.S. launch of Conexxence and Bomyntra follows the FDA’s approval in March 2025.
By: Rachel Klemovitch
Otulfi was approved in September 2024 by the FDA for both subcutaneous and intravenous formulations as a biosimilar to Stelara.
New algorithm increases plasma collection while maintaining donor safety.
By: Charlie Sternberg
Demonstrates its commitment to providing quality, cost-saving treatment options to clinicians and the patients they serve.
Integration of Ori's IRO Platform with Cue and Lovo processing systems aims to enhance efficiency in CGT manufacturing.
By: Kristin Brooks
Aim to integrate Fresenius Kabi’s suite of cell therapy processing technologies within Cellular Origins’ CGT robotic manufacturing platform Constellation.
Aim to provide cost-effective, high-quality biosimilar treatments that address critical unmet needs in oncology care.
Jurgen Van Broeck brings experience and a proven track record in the pharmaceutical and biosimilar industries.
Signals a step in mAbxience's global expansion strategy and advances Teva’s goal to expand its biosimilar pipeline through business development.
Serves as a generic substitute for Cytoxan, for use in treating several forms of cancer.
mAbxience will manufacture the active ingredient Agalsidase Beta, developed by Biosidus as a biosimilar of Fabrazyme for the treatment of Fabry disease.
Invests nearly $1 billion to double U.S. manufacturing capacity and enhance production and distribution network.
Companies are looking to diversify their API suppliers and manufacturers to different locations instead of outsourcing it to just one manufacturer.
By: Grandview Research
Expands global presence and adds significant capacity for sterile liquid manufacturing.
By: Anthony Vecchione
Aims to help lessen the manufacturing barriers for cell and gene therapies by integrating cutting-edge automation tools.
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