Theravance Biopharma
75
1
2
66
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
Moderate Risk
Score: 35/100
9.3%
7 terminated/withdrawn out of 75 trials
90.4%
+3.9% vs industry average
16%
12 trials in Phase 3/4
39%
26 of 66 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (75)
Phase 3 Efficacy and Durability of Ampreloxetine for the Treatment of Symptomatic nOH in Participants With Multiple System Atrophy
Role: lead
Compare the Effects of Nebulizer Versus Inhaler Based Therapy for COPD Using Long-acting Bronchodilators
Role: collaborator
Revefenacin in Acute Respiratory Insufficiency in COPD
Role: collaborator
Evaluate the Safety and Efficacy of a 5-HT4 Agonist in Chronic Constipation (ACCORD Trial)
Role: collaborator
Safety, Pharmacokinetics and Pharmacodynamics of Velusetrag in Healthy Elderly Subjects
Role: collaborator
Phase 4 COPD and Suboptimal Inspiratory Flow Rate
Role: lead
Efficacy and Safety of TD-1473 in Crohn's Disease
Role: lead
Phase 3 Clinical Effect Durability of TD-9855 for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
Role: lead
Phase 3 Open-Label Extension Study of TD-9855 for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
Role: lead
Efficacy & Safety of TD-1473 in Ulcerative Colitis
Role: lead
TD-1473 Long-Term Safety (LTS) Ulcerative Colitis (UC) Study
Role: lead
TD-9855 Phase 2 in Neurogenic Orthostatic Hypotension (nOH)
Role: lead
Clinical Effect of Ampreloxetine (TD-9855) for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
Role: lead
A Study of TD-9855 in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)
Role: lead
Effect of Inhaled TD-8236 on Allergen-induced Asthmatic Response
Role: lead
TD-0903 for ALI Associated With COVID-19
Role: lead
Phase 2 Study of TD-9855 to Treat Fibromyalgia
Role: lead
A 42-day Parallel Group Safety Study of Revefenacin and Formoterol, Administered in Sequence and as a Combination, in Participants With COPD
Role: collaborator
Revefenacin Peak Inspiratory Flow Rate (PIFR) Study in COPD
Role: collaborator
A 28-Day Parallel Group Study of TD-4208 in Chronic Obstructive Pulmonary Disease (COPD)
Role: collaborator