Learn languages naturally with fresh, real content!

Popular Topics
Explore By Region
U.S. FDA accepted leniolisib application for children 4–11 with rare immune disorder APDS, with decision due Jan. 31, 2026.
The U.S. FDA has accepted Pharming Group’s supplemental drug application for leniolisib, an oral PI3Kδ inhibitor, for children aged 4 to 11 with activated PI3Kδ syndrome (APDS), a rare immune disorder.
The application received Priority Review, with a decision expected by January 31, 2026.
Data from a Phase III trial showed improved disease markers—reduced lymphadenopathy and increased naïve B cells—within 12 weeks, along with eight months of safety data.
If approved, leniolisib would be the first treatment for children under 12 with APDS globally.
The drug, already approved for those 12 and older, is under review in several other countries.
APDS, caused by genetic mutations, leads to recurrent infections, immune dysfunction, and long-term complications like lymphoma and lung damage, often diagnosed years after symptoms begin.
La FDA de los Estados Unidos aceptó la solicitud de leniolisib para niños de 4 a 11 años con trastorno inmunológico raro APDS, con decisión prevista para el 31 de enero de 2026.