Monoclonal antibodies lead biosimilar approvals because of their large market size, well-defined regulatory pathways, and ...

Tendering emerged as the most effective strategy for reducing costs and increasing biosimilar uptake in the retail setting, ...

Patients with diabetic macular edema previously treated with a ranibizumab biosimilar in India experience comparable safety ...

The introduction of biosimilars in the treatment of age-related macular degeneration (AMD) is raising concerns among ...

Biocon’s ustekinumab biosimilar matched reference ustekinumab in efficacy and safety, while an adalimumab biosimilar proved ...

Global biosimilar regulatory harmonization will be needed to reduce development costs and improve patient access, despite ...

Although more research is needed in pediatric patients, biosimilars could improve treatment access and reduce costs.

Number 3: The denosumab biosimilar market is poised for disruption with 3 FDA-approved biosimilars, at least 5 awaiting approval, and launches anticipated to start in May 2025, while ongoing patent ...

Celltrion and Formycon with Fresenius Kabi launched their respective ustekinumab biosimilars (Steqeyma and Otulfi), joining 4 ...

The denosumab biosimilar market is poised for disruption with 3 FDA-approved biosimilars, at least 5 awaiting approval, and ...