Theravance Biopharma (TBPH) released a presentation on August 25 covering its Phase 3 CYPRESS study (0197) of ampreloxetine, an experimental drug for symptomatic neurogenic orthostatic hypotension (nOH) — the blood pressure drops experienced by patients with multiple system atrophy (MSA). The deck includes post hoc (after-the-fact) analyses of the study data, plus details on the company's interactions with the U.S. FDA regarding the drug's development program. Keep in mind, though, that the 8-K text itself only states the presentation was "made available" — the actual data and FDA talking points sit in the attached exhibit, so the filing doesn't spell out any conclusions.
View Full Filing (SEC EDGAR)