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A Phase 3, 22-week, Multi-center, Randomized Withdrawal Study of TD-9855 in Treating Symptomatic Neurogenic Orthostatic Hypotension in Subjects With Primary Autonomic Failure

Trial Profile

A Phase 3, 22-week, Multi-center, Randomized Withdrawal Study of TD-9855 in Treating Symptomatic Neurogenic Orthostatic Hypotension in Subjects With Primary Autonomic Failure

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 09 Apr 2025

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At a glance

  • Drugs Ampreloxetine (Primary)
  • Indications Orthostatic hypotension
  • Focus Registrational; Therapeutic Use
  • Acronyms REDWOOD
  • Sponsors Theravance Biopharma

Most Recent Events

  • 07 Apr 2025 According to a Theravance Biopharma media release, results form these studies supported registrational study in patients with nOH and MSA, CYPRESS currently ongoing.
  • 07 Apr 2025 According to a Theravance Biopharma media release, new analysis form Study 0169 and Study 170 were presented at the 77th Annual Meeting of the American Academy of Neurology (AAN) Meeting.
  • 07 Apr 2025 Results presented in the Theravance Biopharma Media Release.

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