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USV, Biogenomics launch INSUQUICK, biosimilar Insulin Aspart for diabetes treatment

Express Pharma

USV and Biogenomics announced the launch of INSUQUICK, biosimilar Insulin Aspart. Insuquick will be available in cartridges, vials, and prefilled disposable pens, offering flexibility tailored to the needs of people with diabetes. It is available in all metros, and Tier I/II cities.”

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Glenmark launches biosimilar of anti-diabetic drug, Liraglutide, in India

Express Pharma

Glenmark Pharmaceuticals has launched a biosimilar of anti-diabetic drug, Liraglutide, in India. It has been approved globally for the management of type 2 diabetes mellitus in adult patients in the US and the EU. Liraglutide has a proven efficacy in improving glycemic control in patients with type 2 diabetes mellitus.

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Opinion: Market share isn’t the only metric for biosimilars’ success

STAT

Market share is often held up as the most relevant metric for the success of a biosimilar class. I believe there are other metrics, like cost savings or signs of greater patient access, that should also be used to define biosimilars’ successes or failures. the first biosimilar was launched in September 2015. In the U.S.,

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Recent Biosimilar Approvals By the FDA

Big Molecule Watch

Approval of Accord’s Trastuzumab Biosimilar : On September 18, 2024, Accord announced that the Food and Drug Administration (FDA) approved a 420 mg dosage of HERCESSI (trastuzumab-strf), a biosimilar to Genentech’s HERCEPTIN (trastuzumab), to treat HER2-overexpressing breast and gastric or gastroesophageal junction adenocarcinoma.

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Biocon Biologics report explores pathways to increase biosimilar adoption in low- and middle-income countries

Express Pharma

Biocon Biologics, a global biosimilars company, has released the findings of a study focused on improving the adoption of biosimilars in low- and middle-income countries (LMICs). ” The study outlines six policy recommendations aimed at increasing access to and usage of quality-assured biosimilars in LMICs.

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Aflibercept Biosimilar Updates in Europe

Big Molecule Watch

On September 19, 2024, the European Medicines Agency (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion for Sandoz’s aflibercept biosimilar AFQLIR. On September 20, 2024, Samsung and Biogen announced that the CHMP also adopted a positive opinion for their aflibercept biosimilar OPUVIZ.

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Lupin completes Phase 3 Trials for Lucentis Biosimilar

Express Pharma

Lupin announced the completion of a global Phase 3 clinical study of LUBT010, its biosimilar candidate to Lucentis. Lupin has been marketing its ranibizumab biosimilar in India under the brand name RaniEyes since 2022. The post Lupin completes Phase 3 Trials for Lucentis Biosimilar appeared first on Express Pharma.