Theravance Biopharma
Trial Pipeline
Phase 3 Efficacy and Durability of Ampreloxetine for the Treatment of Symptomatic nOH in Participants With Multiple System Atrophy
NCT05696717
TD-0903 for ALI Associated With COVID-19
NCT04402866
Clinical Effect of Ampreloxetine (TD-9855) for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
NCT03750552
Multiple Dose Ethnobridging PK Study in Healthy Subjects
NCT03750565
Drug-Drug Interaction (DDI) Study for TD-9855
NCT03432793
Multiple Ascending Dose Study of TD-1439 in Healthy Adult and Elderly Subjects
NCT02954263
Multiple Ascending Dose Study of TD-0714 in Healthy and Elderly Subjects
NCT02709928
Single Ascending Dose Study of TD-0714 in Healthy Subjects
NCT02639078
TD-6450 MAD Study in HCV Infected Subjects
NCT02116543
TD-6450 SAD and MAD in Healthy Subjects
NCT02022306
TD-9855 Mass Balance Study
NCT01924143
A Study of TD-9855 in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)
NCT01458340
A Study of TD-1211 in Subjects With Opioid-Induced Constipation (OIC)
NCT01401985
TD-1792 in Gram-positive Complicated Skin and Skin Structure Infection
NCT00442832
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 8 |
| Phase 2 | 4 |
| Phase 3 | 2 |
Therapeutic Areas
What the Pipeline for Theravance Biopharma Shows
According to the ClinicalTrials.gov registry, Theravance Biopharma is linked to 14 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting — about 0% of the sponsor's indexed portfolio — and 13 are already marked complete, representing roughly 93% of the total. Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
The phase mix for Theravance Biopharma reports 2 late-stage studies (Phase 3 and Phase 4 combined) and 12 earlier-phase studies (Phase 1 and Phase 2). A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work — safety, dosing, and early signal detection — and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
The top therapeutic focus area indexed for Theravance Biopharma is Healthy Adults, Elderly Subjects with 2 linked trials, and 9 other condition areas appear in the top list above. That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice — verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology — how this data is sourced, computed, and verified.