PRESS RELEASE published on 07/26/2024 at 12:00, 1 year 4 months ago Formycon and Fresenius Kabi receive positive CHMP opinion for FYB202 (Ustekinumab), a biosimilar candidate to Stelara® Formycon and Fresenius Kabi receive positive CHMP opinion for FYB202 biosimilar candidate to Stelara. Approval expected in early Q4 2024. Biosimilars boost healthcare access & reduce costs globally Biosimilar Formycon Fresenius Kabi FYB202 CHMP Opinion
BRIEF published on 07/26/2024 at 10:59, 1 year 4 months ago FYB202 Biosimilar to Stelara Receives Positive CHMP Opinion from EMA Biosimilar Formycon FYB202 CHMP EMA
BRIEF published on 07/26/2024 at 10:59, 1 year 4 months ago Le biosimilaire FYB202 de Stelara reçoit un avis positif du CHMP de l'EMA Formycon FYB202 Biosimilaire CHMP EMA
PRESS RELEASE published on 07/26/2024 at 10:54, 1 year 4 months ago EQS-Adhoc: Stelara® Biosimilar Candidate FYB202 (Ustekinumab) receives positive CHMP opinion from EMA Formycon AG's biosimilar candidate FYB202 (Ustekinumab) for Stelara® receives a positive opinion from EMA's CHMP, recommended for EU approval for treating severe inflammatory diseases Formycon AG Biosimilar FYB202 CHMP EMA
BRIEF published on 07/01/2024 at 06:55, 1 year 5 months ago Formycon Receives FDA Approval for Aflibercept Biosimilar FDA Approval Biosimilar Formycon Retinal Diseases Ophthalmic Therapies
BRIEF published on 07/01/2024 at 06:55, 1 year 5 months ago Formycon reçoit l'approbation de la FDA pour le biosimilaire Aflibercept Approbation De La FDA Formycon Biosimilaire Maladies De La Rétine Thérapies Ophtalmiques
PRESS RELEASE published on 07/01/2024 at 06:50, 1 year 5 months ago Formycon receives FDA approval for FYB203/AHZANTIVE®1) (aflibercept-mrbb), a biosimilar to Eylea®2) Formycon receives FDA approval for FYB203/AHZANTIVE(R) (aflibercept-mrbb), a biosimilar to Eylea(R). The approval highlights Formycon's expertise and commitment to providing effective and affordable biosimilar therapies for retinal diseases. FDA Approval Biosimilar Formycon Eylea Retinal Diseases
BRIEF published on 06/28/2024 at 23:55, 1 year 5 months ago FDA Approves Biosimilar FYB203/AHZANTIVE® for Retinal Diseases FDA Approval Biosimilar Eylea Retinal Diseases Treatment Approval
BRIEF published on 06/28/2024 at 23:55, 1 year 5 months ago La FDA approuve le biosimilaire FYB203/AHZANTIVE® pour les maladies rétiniennes Approbation De La FDA Biosimilaire Eylea Maladies De La Rétine Approbation Du Traitement
PRESS RELEASE published on 06/28/2024 at 23:50, 1 year 5 months ago EQS-Adhoc: FDA grants approval for Eylea®1) biosimilar FYB203/AHZANTIVE®2) (aflibercept-mrbb) FDA grants approval for Eylea biosimilar FYB203/AHZANTIVE by Formycon AG and Klinge Biopharma GmbH. Biosimilar approved for nAMD and other retinal diseases FDA Approval Retinal Diseases Eylea Biosimilar FYB203/AHZANTIVE Neovascular Age-Related Macular Degeneration
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