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Cosmo and Takeda Renew Strategic Manufacturing Agreement for Global Supply of Oral Treatment for Ulcerative Colitis

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Cosmo Pharmaceuticals (OTC:CMOPF) has renewed its strategic manufacturing agreement with Takeda (NYSE:TAK) for the production of Mesalazine MMX 1200 mg, marketed as Lialda in the USA and Mezavant in Europe, for ulcerative colitis treatment.

The multi-year agreement will be executed at Cosmo's 18,000 m² manufacturing facility in Lainate, Italy, which is ISO 13485 certified and approved by multiple regulatory authorities worldwide. The facility has been supporting global pharmaceutical production for over 30 years.

This renewal aligns with Cosmo's Vision 2030 strategy to expand trusted partnerships and strengthen its Contract Development and Manufacturing Organization (CDMO) leadership globally.

Cosmo Pharmaceuticals (OTC:CMOPF) ha rinnovato il suo accordo strategico di produzione con Takeda (NYSE:TAK) per la realizzazione di Mesalazina MMX 1200 mg, commercializzata come Lialda negli USA e Mezavant in Europa, per il trattamento della colite ulcerosa.

Il contratto pluriennale sarà eseguito presso l'impianto produttivo di 18.000 m² di Cosmo a Lainate, Italia, certificato ISO 13485 e approvato da numerose autorità regolatorie a livello globale. Questa struttura supporta la produzione farmaceutica mondiale da oltre 30 anni.

Il rinnovo si inserisce nella strategia Vision 2030 di Cosmo, che punta ad ampliare partnership affidabili e a rafforzare la sua leadership come Contract Development and Manufacturing Organization (CDMO) a livello internazionale.

Cosmo Pharmaceuticals (OTC:CMOPF) ha renovado su acuerdo estratégico de fabricación con Takeda (NYSE:TAK) para la producción de Mesalazina MMX 1200 mg, comercializada como Lialda en EE. UU. y Mezavant en Europa, para el tratamiento de la colitis ulcerosa.

El acuerdo plurianual se llevará a cabo en la planta de fabricación de 18,000 m² de Cosmo en Lainate, Italia, certificada ISO 13485 y aprobada por múltiples autoridades regulatorias a nivel mundial. La instalación ha apoyado la producción farmacéutica global durante más de 30 años.

Esta renovación está alineada con la estrategia Vision 2030 de Cosmo, que busca expandir asociaciones confiables y fortalecer su liderazgo en Contract Development and Manufacturing Organization (CDMO) a nivel global.

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ì´ë²ˆ 계약 ê°±ì‹ ì€ ì‹ ë¢°í•� ìˆ� 있는 파트너십ì� 확대하고 ì � 세계ì ìœ¼ë¡� Contract Development and Manufacturing Organization (CDMO) 리ë”ì‹­ì„ ê°•í™”í•˜ë ¤ëŠ� Cosmoì� Vision 2030 ì „ëžµê³� ì¼ì¹˜í•©ë‹ˆë‹�.

Cosmo Pharmaceuticals (OTC:CMOPF) a renouvelé son accord stratégique de fabrication avec Takeda (NYSE:TAK) pour la production de Mesalazine MMX 1200 mg, commercialisée sous le nom de Lialda aux États-Unis et Mezavant en Europe, pour le traitement de la colite ulcéreuse.

L'accord pluriannuel sera exécuté dans l'installation de fabrication de 18 000 m² de Cosmo à Lainate, en Italie, certifiée ISO 13485 et approuvée par plusieurs autorités réglementaires à travers le monde. Cette installation soutient la production pharmaceutique mondiale depuis plus de 30 ans.

Ce renouvellement s'inscrit dans la stratégie Vision 2030 de Cosmo, visant à étendre des partenariats de confiance et à renforcer son leadership en tant qu'Organisation de Développement et de Fabrication sous Contrat (CDMO) à l'échelle mondiale.

Cosmo Pharmaceuticals (OTC:CMOPF) hat seine strategische Fertigungsvereinbarung mit Takeda (NYSE:TAK) für die Herstellung von Mesalazin MMX 1200 mg erneuert, das in den USA als Lialda und in Europa als Mezavant zur Behandlung von Colitis ulcerosa vermarktet wird.

Die mehrjährige Vereinbarung wird in der 18.000 m² großen Produktionsstätte von Cosmo in Lainate, Italien umgesetzt, die ISO 13485 zertifiziert ist und von mehreren weltweiten Regulierungsbehörden zugelassen wurde. Die Anlage unterstützt seit über 30 Jahren die globale pharmazeutische Produktion.

Diese Erneuerung steht im Einklang mit Cosmos Vision 2030-Strategie, vertrauenswürdige Partnerschaften auszubauen und seine Führungsposition als Contract Development and Manufacturing Organization (CDMO) weltweit zu stärken.

Positive
  • Renewal of strategic manufacturing partnership with major pharmaceutical company Takeda
  • Reinforces Cosmo's position as a trusted global manufacturing partner
  • Alignment with Vision 2030 strategy for CDMO leadership expansion
  • Manufacturing facility has regulatory approvals from multiple global authorities
Negative
  • None.

Dublin, Ireland--(Newsfile Corp. - August 8, 2025) - Cosmo Pharmaceuticals N.V. (SIX: COPN), a global leader in AI-driven healthcare and specialty pharmaceuticals, today announced the renewal of its multi-year manufacturing and supply agreement with Takeda (TSE: 4502) (NYSE: TAK), to produce Mesalazine MMX 1200 mg (marketed as Lialda® in the USA and as Mezavant in Europe) oral, once-daily treatment for ulcerative colitis, reinforcing its position as a trusted partner for global production of key medicines.

“This renewal underscores our long-standing collaboration with Takeda and our best-in-class manufacturing capabilities,” said Giovanni Di Napoli, CEO of Cosmo. “We are proud of the trust our partners place in our R&D expertise and our ability to deliver high-quality pharmaceutical solutions. This agreement further strengthens our commitment to innovation, sustainability, and excellence, and it aligns perfectly with our Vision 2030 strategy to scale trusted partnerships and grow our CDMO leadership globally.”

Cosmo’s advanced manufacturing site in Lainate (Italy) is approved by multiple regulatory authorities worldwide. It continues to play a key role in supporting global pharmaceutical players, thereby ensuring efficient and environmentally responsible production and excellent supply chain for more than 30 years. The quality system of the 18.000 m² site is certified in accordance with the ISO 13485 standards and is focused on continuous improvement and customer satisfaction. 

About Cosmo

Cosmo is a life sciences company focused on MedTech AI, dermatology, gastrointestinal diseases, and contract development and manufacturing (CDMO). We design, develop, and manufacture advanced solutions that address critical medical needs and raise the standard of care. Our technologies are trusted by leading global pharmaceutical and MedTech companies and reach patients and healthcare providers around the world. Guided by our purpose - Building Health Confidence - our mission is to empower patients, healthcare professionals, and partners by innovating at the intersection of science and technology. Founded in 1997, Cosmo is headquartered in Dublin, Ireland, with offices in San Diego (USA), and in Lainate, Rome, and Catania (Italy).
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FAQ

What is the new manufacturing agreement between Cosmo Pharmaceuticals (CMOPF) and Takeda?

Cosmo has renewed its multi-year manufacturing agreement with Takeda to produce Mesalazine MMX 1200 mg, marketed as Lialda in the USA and Mezavant in Europe, for ulcerative colitis treatment.

Where will Cosmo manufacture the ulcerative colitis treatment for Takeda?

The manufacturing will take place at Cosmo's 18,000 m² ISO 13485-certified facility in Lainate, Italy, which has been operating for over 30 years.

How does this agreement align with Cosmo's business strategy?

The agreement aligns with Cosmo's Vision 2030 strategy to scale trusted partnerships and grow their CDMO leadership position globally.

What certifications does Cosmo's manufacturing facility have?

Cosmo's Lainate facility is ISO 13485 certified and approved by multiple regulatory authorities worldwide, focusing on continuous improvement and customer satisfaction.
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