Teva expands European biosimilars push with AHZANTIVE launch for eye disease treatment
Teva said the launch strengthens its biosimilars strategy and expands access to biologic medicines across Europe
Teva said the launch strengthens its biosimilars strategy and expands access to biologic medicines across Europe
The JADE trial enrolled 164 U.S. patients who initially received three monthly doses of OLN324 or faricimab, followed by 12 weeks off treatment with retreatment allowed only if disease recurred
The trial, dubbed MALBEC, marks the first in a broader late-phase development push for MK-8748, with a second NVAMD study expected to begin later this year
Eylea 2mg (intravitreal aflibercept injection) is an anti-VEGF therapy that blocks a protein responsible for abnormal blood vessel growth and leakage in the retina
The biotechnology company will tap into Catalent’s expertise in induced pluripotent stem cells and advanced cell-therapy manufacturing
ANYRA is India’s first indigenously developed Aflibercept 2 mg biosimilar
The company is rolling out ARTEMIS, a next-generation AI platform for capsid design
DME is among the most challenging retinal diseases to treat and has long served as a proving ground for therapies that ultimately become first-line standard of care in retinal diseases
Under the agreement, AVT06 is licensed to enter the US market in the fourth quarter of 2026
Yesafili, available in vial and prefilled syringe presentations (2 mg/0.05 mL), was the first biosimilar to Eylea approved by Health Canada
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