Meiji Seika Pharma said on July 14 that its biosimilar version of Stelara (ustekinumab) being jointly developed with South Korean partner Dong-A ST has been accepted for European regulatory review. The Stelara biosimilar, DMB-3115, was filed with the European Medicines…
To read the full story
Related Article
- US FDA Accepts Stelara Biosimilar for Review: Meiji
January 9, 2024
- Meiji’s Stelara Biosimilar Shows Therapeutic Equivalence; Filing Eyed in 2023
January 23, 2023
- Meiji Kicks Off Japanese PI Study of Stelara Biosimilar
May 12, 2022
BUSINESS
- Sanofi Bets on Immunotherapy to Delay Onset of Type 1 Diabetes
December 19, 2025
- Japan’s 1st Eylea Biosimilar to Reach Market on January 7
December 19, 2025
- Padcev-Keytruda Pair Makes Mark in Cisplatin-Eligible MIBC: Astellas
December 19, 2025
- Daiichi Sets February Launch for Japan’s 1st OTC Morning-After Pill
December 19, 2025
- Takeda’s TYK2 Inhibitor Scores PIII Win in Psoriasis Trials, Tops Otezla on Key Metrics
December 19, 2025
Let’s be real: even with the best intentions, AI systems can reflect our own unconscious biases. As Daniel Kahneman and Amos Tversky famously demonstrated in their groundbreaking work on Prospect Theory, humans are prone to cognitive biases that influence our…





