Theravance Shares Presentation on Phase 3 CYPRESS Study of Amppreloxetine
On August 25, 2026, Theravance Biopharma made available a presentation on its Phase 3 CYPRESS Study (0197) evaluating ampreloxetine in patients with symptomatic neurogenic orthostatic hypotension associated with multiple system atrophy. The materials include post hoc analyses of CYPRESS data and information about the company’s interactions with the U.S. Food and Drug Administration regarding ampreloxetine’s clinical development program.