28 January 2026 - Tenpoint Therapeutics today announced that the US FDA approved Yuvezza (carbachol and brimonidine tartrate ophthalmic solution) 2.75%/0.1%, previously known as Brimochol PF, the first and only dual agent eye drop for the treatment of presbyopia in adults.
Yuvezza is expected to be broadly commercially available in the US in Q2, 2026.