Sandoz’s CIMERLI comes in two concentrations, 6mg/mL and 10mg/mL. Credit: megaflopp / Shutterstock.com.
Sandoz has concluded the acquisition of the US biosimilar CIMERLI from Coherus BioSciences, marking a significant expansion of its ophthalmology and biosimilar expertise in the US market.
The transaction, valued at $170m in upfront cash, encompasses the full CIMERLI business, including a biologics licence application, product inventory, specialised commercial software, ophthalmology sales and field reimbursement talent.
Approved by the FDA in August 2022 and launched two months later, CIMERLI met the regulator’s standards of biosimilarities, including safety, efficacy and quality.
It is the first and only FDA-approved biosimilar interchangeable with LUCENTIS for all its indications.
Sandoz North America president Keren Haruvi stated: “Today, we further expand the SandozSandoz biosimilar portfolio while advancing our mission in the US of pioneering patient access to more affordable and much-needed medicines.
“With the addition of CIMERLI to our existing ophthalmology franchise, we can now offer even more treatment options for US patients with vision impairment and loss.”
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