PRESS RELEASE published on 02/17/2025 at 08:05, 1 year 1 month ago EQS-Adhoc: Formycon announces decision on Phase III trial with FYB206 and provides update on potential need to adjust the valuation of FYB202 and FYB201 Formycon terminates Phase III trial for FYB206 after FDA feedback, anticipates valuation adjustments for FYB202 & FYB201 due to price discounts FDA Feedback Valuation Adjustments Formycon FYB206 Price Discounts
BRIEF published on 02/05/2025 at 06:35, 1 year 1 month ago Lotus Pharmaceutical Partners with Formycon to Commercialize Eylea® Biosimilar in Asia-Pacific Lotus Pharmaceutical Eylea® Biosimilar Asia-Pacific Commercialization FDA And EU Approval Retinal Disease Treatment
BRIEF published on 02/05/2025 at 06:35, 1 year 1 month ago Lotus Pharmaceutical s'associe à Formycon pour commercialiser le biosimilaire Eylea® en Asie-Pacifique Lotus Pharmaceutique Biosimilaire Eylea® Commercialisation En Asie-Pacifique Approbation De La FDA Et De L'UE Traitement Des Maladies De La Rétine
PRESS RELEASE published on 02/05/2025 at 06:30, 1 year 1 month ago Lotus Pharmaceutical becomes strategic partner for the commercialization of Formycon’s Eylea® biosimilar FYB203/AHZANTIVE® in the Asia-Pacific Region Formycon AG announces strategic partnership with Lotus Pharmaceutical for commercialization of Eylea biosimilar FYB203/AHZANTIVE in Asia-Pacific region Formycon AG Asia-Pacific Eylea Biosimilar FYB203/AHZANTIVE Lotus Pharmaceutical
BRIEF published on 01/20/2025 at 06:35, 1 year 2 months ago Formycon Secures EU Approval for Biosimilar FYB203 Formycon AG EU Approval Teva Pharmaceuticals Aflibercept Biosimilar FYB203
BRIEF published on 01/20/2025 at 06:35, 1 year 2 months ago Formycon obtient l'approbation de l'UE pour le biosimilaire FYB203 Formycon AG Teva Pharmaceuticals Aflibercept Homologation UE Biosimilaire FYB203
PRESS RELEASE published on 01/20/2025 at 06:30, 1 year 2 months ago Formycon receives EU approval for FYB203 (aflibercept), a biosimilar to Eylea®, under the brand names AHZANTIVE® and Baiama® Formycon receives EU approval for biosimilar FYB203 (aflibercept) to Eylea®, brands AHZANTIVE® and Baiama® for nAMD and retinal diseases. Teva to market AHZANTIVE® in Europe Biosimilar Formycon EU Approval AHZANTIVE Baiama
BRIEF published on 01/15/2025 at 06:35, 1 year 2 months ago MHRA Grants Approval for Formycon and Fresenius Kabi's Otulfi® Formycon Fresenius Kabi Ustekinumab Biosimilar Approval Otulfi® Launch
BRIEF published on 01/15/2025 at 06:35, 1 year 2 months ago La MHRA accorde son approbation à Formycon et à Otulfi® de Fresenius Kabi Formycon Fresenius Kabi Ustekinumab Approbation Des Biosimilaires Lancement D'Otulfi®
PRESS RELEASE published on 01/15/2025 at 06:30, 1 year 2 months ago Formycon and Fresenius Kabi announce MHRA approval for FYB202/Otulfi® (ustekinumab), a biosimilar to Stelara® Formycon and Fresenius Kabi announce MHRA approval for FYB202/Otulfi®, a biosimilar to Stelara®, for various inflammatory diseases. Global biosimilar approval news Biosimilar Formycon Fresenius Kabi FYB202 MHRA Approval
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