Asitri Dashboard

Search Clinical Trials

The U.S. National Library of Medicine provides a database of clinical trials worldwide. Use the fields below to search the database. Expand your results and select terms or phrases and right-click to search using Google, MalaCards, MedlinePlus, PubMed, or Wikipedia.

Saved Searches

Choose Search
Basic Search
Targeted Search

Clinical Trials Search Results

Search History:
Count: 74
Selected: 0
NCT IDTitle
NCT04681079Comparison of Viral Particle Dispersion Following Administration of an MDI or Nebulizer in Subjects With COVID-19
NCT02820311Thorough QT (TQT) Study of TD-4208 in Healthy Subjects
NCT02657122SAD and MAD Study to Evaluate Safety, Tolerability, and Pharmacokinetics (PK) of TD-1473 in Healthy Subjects
NCT01321879Study to Evaluate the Safety and Efficacy of Telavancin in the Treatment of Gram Positive Bloodstream Infections in Cancer Patients
NCT02392208Effect of Dialysis on the Pharmacokinetics of Telavancin in Patients With Chronic Kidney Disease Stage 5
NCT01040637A Multiple Dose Study of TD-1211 in Healthy Volunteers and Patients With Opioid-Induced Constipation
NCT01644240A Phase 1, Multiple Intravenous Dose Study to Examine Safety, Tolerability, and PK of Intravenous TD-8954, a 5-HT4 Receptor Agonist, in Healthy Subjects
NCT00550225Succinate Salt Version of GSK961081 for Healthy Volunteers
NCT01718938Phase 2 Study of Velusetrag in Diabetic or Idiopathic Gastroparesis
NCT02116543TD-6450 MAD Study in HCV Infected Subjects
NCT02581592Pharmacokinetics of TD-4208 in Patients With Moderate Hepatic Impairment
NCT02040792A 28-Day Parallel Group Study of TD-4208 in Chronic Obstructive Pulmonary Disease (COPD)
NCT03829657Phase 3 Clinical Effect Durability of TD-9855 for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
NCT03573817A 42-day Parallel Group Safety Study of Revefenacin and Formoterol, Administered in Sequence and as a Combination, in Participants With COPD
NCT04200573Effect of Hepatic Impairment on the Pharmacokinetics of a Single Dose of TD-9855
NCT02022306TD-6450 SAD and MAD in Healthy Subjects
NCT04589260TD-1058 First-In-Human Study in Healthy Subjects and Subjects With Idiopathic Pulmonary Fibrosis
NCT04688632Thorough QT Study to Evaluate Ampreloxetine in Healthy Subjects
NCT01458340A Study of TD-9855 in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)
NCT01459926A Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study to Assess the Safety and Efficacy of TD-1211 in Subjects With Opioid-Induced Constipation
NCT02518139A 52-Week Parallel Group Safety Study of TD-4208 in Chronic Obstructive Pulmonary Disease (COPD)
NCT01568411A Fixed-Sequence, Two-Period, Open-Label Drug-Drug Interaction Study to Assess the Effect of an Inhibitor of Cytochrome P450 Isoenzyme 3A4 and Permeability Glycoprotein 1 on the Pharmacokinetics of TD-1211
NCT02109172A 7-Day Cross-over Study of QD (Once Daily) and BID (Twice Daily) TD-4208 in Chronic Obstructive Pulmonary Disease (COPD)
NCT03750565Multiple Dose Ethnobridging PK Study in Healthy Subjects
NCT03103412TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC)
NCT01791049TD-1607 SAD Study in Healthy Subjects
NCT02512510Efficacy Study of Nebulized TD-4208 for Chronic Obstructive Pulmonary Disease (COPD)
NCT05696717Phase 3 Efficacy and Durability of Ampreloxetine for the Treatment of Symptomatic nOH in Participants With Multiple System Atrophy
NCT04402866TD-0903 for ALI Associated With COVID-19
NCT00887406Study of GSK961081 in Healthy Volunteer Subjects
NCT02772159TD-4208 Absorption, Distribution, Metabolism and Excretion (ADME) Study in Healthy Male Subjects
NCT03432793Drug-Drug Interaction (DDI) Study for TD-9855
NCT01924143TD-9855 Mass Balance Study
NCT02954263Multiple Ascending Dose Study of TD-1439 in Healthy Adult and Elderly Subjects
NCT02663089A Phase 1 (Ph1), Single Dose (SD), GSK961081 Absorption, Distribution, Metabolism, and Excretion (ADME) Study in Healthy Subjects
NCT017044047 Days of TD-4208 in Subjects With Chronic Obstructive Pulmonary Disease
NCT03095456Revefenacin Peak Inspiratory Flow Rate (PIFR) Study in COPD
NCT02639078Single Ascending Dose Study of TD-0714 in Healthy Subjects
NCT04587713Single Dose Bioavailability and Ethnobridging PK Study in Healthy Subjects
NCT02903095Single Ascending Dose Study of TD-1439 in Healthy Subjects
NCT04315558Revefenacin in Acute Respiratory Insufficiency in COPD
NCT03750552Clinical Effect of Ampreloxetine (TD-9855) for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
NCT02753855Pharmacokinetics of Telavancin in Normal and Obese Subjects
NCT03920254TD-1473 Long-Term Safety (LTS) Ulcerative Colitis (UC) Study
NCT03408470TD-1473 Absorption, Distribution, Metabolism and Excretion (ADME) Study in Healthy Male Subjects
NCT03652038Single and Multiple Ascending Dose Study of TD-8236 by Inhalation
NCT04095793Phase 3 Open-Label Extension Study of TD-9855 for Treating Symptomatic nOH in Subjects With Primary Autonomic Failure
NCT01949103TD-1607 MAD Study in Healthy Subjects
NCT00687700A Study to Investigate the Pharmacology of a Dual Pharmacophore in Healthy Volunteers
NCT04150341Effect of Inhaled TD-8236 on Allergen-induced Asthmatic Response