PROSERA Study Enrollment Success
Gossamer Bio achieved a significant milestone by nearing the completion of enrollment for the PROSERA study with 343 patients. The baseline characteristics of the patients are exactly as targeted, enhancing the likelihood of success.
Strong Financial Position
Gossamer Bio ended the quarter with $257.9 million in cash and cash equivalents, providing sufficient capital until the first half of 2027.
Potential Global Expansion
Seralutinib's potential for regulatory approval in Japan is supported by its orphan drug designation and participation of Japanese patients in the PROSERA study.
Strategic Partnership with Chiesi Group
The collaboration with Chiesi Group enables Seralutinib to immediately enter a global registrational Phase III study for PH-ILD, with a shared cost basis of 50-50.