Theravance Biopharma
Theravance Biopharma sponsors 38 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 31 completed. 5 of these trials are in Phase 3-4 (later-stage) and 32 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Healthy Adults, Elderly Subjects, with 2 trials.
Trial Pipeline
38 total, page 1 of 1
Phase 3 Efficacy and Durability of Ampreloxetine for the Treatment of Symptomatic nOH in Participants With Multiple System Atrophy
NCT05696717
Phase 4 COPD and Suboptimal Inspiratory Flow Rate
NCT05165485
TD-0903 Pharmacokinetics Study in Healthy Participants With Supplemental Oxygenation
NCT05091723
Comparison of Viral Particle Dispersion Following Administration of an MDI or Nebulizer in Subjects With COVID-19
NCT04681079
Thorough QT Study to Evaluate Ampreloxetine in Healthy Subjects
NCT04688632
Single Dose Bioavailability and Ethnobridging PK Study in Healthy Subjects
NCT04587713
TD-1473 Long-Term Safety (LTS) Ulcerative Colitis (UC) Study
NCT03920254
TD-0903 for ALI Associated With COVID-19
NCT04402866
Effect of Hepatic Impairment on the Pharmacokinetics of a Single Dose of TD-9855
NCT04200573
Phase 3 Open-Label Extension Study of TD-9855 for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
NCT04095793
Single and Multiple Ascending Dose, First-in- Human Study in Healthy Subjects
NCT04044339
Efficacy & Safety of TD-1473 in Ulcerative Colitis
NCT03758443
Phase 3 Clinical Effect Durability of TD-9855 for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
NCT03829657
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
Efficacy and Safety of TD-1473 in Crohn's Disease
NCT03635112
Food-effect, Drug-Drug Interaction (DDI), and Formulation Bridging Study
NCT03555617
Drug-Drug Interaction (DDI) Study for TD-9855
NCT03432793
TD-1473 Absorption, Distribution, Metabolism and Excretion (ADME) Study in Healthy Male Subjects
NCT03408470
TD-9855 Phase 2 in Neurogenic Orthostatic Hypotension (nOH)
NCT02705755
TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC)
NCT03103412
Multiple Ascending Dose Study of TD-1439 in Healthy Adult and Elderly Subjects
NCT02954263
TD-1473 for Active Ulcerative Colitis (UC)
NCT02818686
Single Ascending Dose Study of TD-1439 in Healthy Subjects
NCT02903095
Multiple Ascending Dose Study of TD-0714 in Healthy and Elderly Subjects
NCT02709928
SAD and MAD Study to Evaluate Safety, Tolerability, and Pharmacokinetics (PK) of TD-1473 in Healthy Subjects
NCT02657122
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
TD-1607 MAD Study in Healthy Subjects
NCT01949103
TD-1607 SAD Study in Healthy Subjects
NCT01791049
Phase 2 Study of Velusetrag in Diabetic or Idiopathic Gastroparesis
NCT01718938
Phase 2 Study of TD-9855 to Treat Fibromyalgia
NCT01693692
A Phase 1, Multiple Intravenous Dose Study to Examine Safety, Tolerability, and PK of Intravenous TD-8954, a 5-HT4 Receptor Agonist, in Healthy Subjects
NCT01644240
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
What the Pipeline for Theravance Biopharma Shows
According to the ClinicalTrials.gov registry, Theravance Biopharma is linked to 38 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 31 are already marked complete, representing roughly 82% of the total.
The phase mix for Theravance Biopharma reports 5 late-stage studies (Phase 3 and Phase 4 combined) and 32 earlier-phase studies (Phase 1 and Phase 2).
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.
How to read these pipeline numbers
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.
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.
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.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.