MedPath

Theravance Biopharma

Ownership
-
Employees
99
Market Cap
-
Website
Introduction

Theravance Biopharma, Inc. is a biopharmaceutical company, which engages in the discovery, research, development, and commercialization of respiratory medicines. It operates through the U.S. and Europe geographical segments. Its products include telavancin under the VIBATIV brand, revefenacin under the TD 4208 brand, and neprilysin. The company was founded in July 2013 and is headquartered in George Town, Cayman Islands.

Clinical Trials

54

Active:0
Completed:46

Trial Phases

4 Phases

Phase 1:33
Phase 2:15
Phase 3:4
+1 more phases

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (53 trials with phase data)• Click on a phase to view related trials

Phase 1
33 (62.3%)
Phase 2
15 (28.3%)
Phase 3
4 (7.5%)
Phase 4
1 (1.9%)

Phase 3 Efficacy and Durability of Ampreloxetine for the Treatment of Symptomatic NOH in Participants with Multiple System Atrophy

Phase 3
Recruiting
Conditions
MSA - Multiple System Atrophy
Symptomatic Neurogenic Orthostatic Hypotension
Interventions
Drug: Placebo
First Posted Date
2023-01-25
Last Posted Date
2024-12-27
Lead Sponsor
Theravance Biopharma
Target Recruit Count
102
Registration Number
NCT05696717
Locations
🇺🇸

Neurostudies, Inc, Port Charlotte, Florida, United States

🇺🇸

Movement Disorders Center of Arizona, Scottsdale, Arizona, United States

🇺🇸

The Parkinson's and Movement Disorder Institute, Fountain Valley, California, United States

and more 66 locations

Phase 4 COPD and Suboptimal Inspiratory Flow Rate

Phase 4
Completed
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
First Posted Date
2021-12-21
Last Posted Date
2024-12-20
Lead Sponsor
Theravance Biopharma
Target Recruit Count
404
Registration Number
NCT05165485
Locations
🇺🇸

Theravance Biopharma Investigational Site site 2, Clearwater, Florida, United States

🇺🇸

Theravance Biopharma Investigational Site, Cudahy, Wisconsin, United States

🇺🇸

Theravance Biopharma Investigational Site #2, Spartanburg, South Carolina, United States

TD-0903 Pharmacokinetics Study in Healthy Participants With Supplemental Oxygenation

Phase 1
Completed
Conditions
Acute Lung Injury (ALI) Due to Coronavirus Disease-2019 (COVID-19)
Interventions
Drug: Nezulcitinib (TD-0903) Dose A
Drug: Nezulcitinib (TD-0903) Dose B
First Posted Date
2021-10-25
Last Posted Date
2021-12-10
Lead Sponsor
Theravance Biopharma
Target Recruit Count
14
Registration Number
NCT05091723
Locations
🇺🇸

Theravance Biopharma Investigational Site, Cypress, California, United States

Thorough QT Study to Evaluate Ampreloxetine in Healthy Subjects

Phase 1
Completed
Conditions
Symptomatic Neurogenic Orthostatic Hypertension
nOH
Interventions
First Posted Date
2020-12-30
Last Posted Date
2021-04-20
Lead Sponsor
Theravance Biopharma
Target Recruit Count
72
Registration Number
NCT04688632
Locations
🇺🇸

Theravance Biopharma Investigational Site, Tempe, Arizona, United States

Comparison of Viral Particle Dispersion Following Administration of an MDI or Nebulizer in Subjects With COVID-19

First Posted Date
2020-12-23
Last Posted Date
2022-01-28
Lead Sponsor
Theravance Biopharma
Target Recruit Count
14
Registration Number
NCT04681079
Locations
🇺🇸

Theravance Biopharma Investigational Site, Kansas City, Kansas, United States

  • Prev
  • 1
  • 2
  • 3
  • 4
  • 5
  • 11
  • Next

News

China Approves First Once-Daily Nebulized LAMA for COPD, Triggering $7.5M Milestone for Theravance

China's NMPA has approved YUPELRI (revefenacin) as the first once-daily nebulized long-acting muscarinic antagonist for maintenance treatment of chronic obstructive pulmonary disease.

Ampreloxetine Shows Promise for Neurogenic Orthostatic Hypotension in MSA Patients Without Worsening Supine Hypertension

New analyses from Theravance Biopharma's Phase 3 trials demonstrate ampreloxetine's selective mechanism of action and durable target engagement in treating neurogenic orthostatic hypotension (nOH) in multiple system atrophy patients.

JAK Inhibitor Pipeline Shows Promise for Autoimmune and Inflammatory Diseases

• The Janus Kinase (JAK) inhibitor pipeline is actively being developed by multiple companies, showing promise in treating various autoimmune and inflammatory diseases. • Key companies such as Incyte, AbbVie, and Bristol Myers Squibb are advancing JAK inhibitor therapies through clinical trials and regulatory submissions. • Emerging therapies like povorcitinib, upadacitinib, and deucravacitinib have demonstrated efficacy in treating conditions like hidradenitis suppurativa, axial spondyloarthritis, and plaque psoriasis. • The JAK inhibitor market is driven by the rising prevalence of chronic diseases and substantial investments in research and development, offering targeted treatment approaches.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.