132 active
/
536 total (since 2015)
25
Phase 1 Active
122 total
57
Phase 2 Active
178 total
37
Phase 3 Active
122 total
26
Phase 4 Active
143 total
Top Sponsors (Industry)
Sorted by active Active Done Failed
AstraZeneca 12 33 3
GSK 5 42 6
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. 5 4 2
Sanofi 4 7 0
Haisco Pharmaceutical Group Co., Ltd. 4 1 0
Roche 3 3 1
Joincare Pharmaceutical Group Industry Co., Ltd 3 1 0
Verona Pharma plc 2 12 0
Mabwell (Shanghai) Bioscience Co., Ltd. 2 2 0
CSPC ZhongQi Pharmaceutical Technology Co., Ltd. 2 0 0
Bambusa Therapeutics 2 0 0
Pulmair Medical, Inc. 2 0 0
Guangdong Hengrui Pharmaceutical Co., Ltd 1 1 0
Pfizer 1 0 1
Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. 1 1 0
NCT06883305 RECRUITING
A Study to Investigate the Efficacy and Safety of Tezepelumab in Adult Participants With Moderate to Very Severe COPD (D5241C00006)
AstraZeneca n=990
NCT06878261 RECRUITING
A Study to Investigate the Efficacy and Safety of Tezepelumab in Adult Participants With Moderate to Very Severe COPD (D5241C00007)
AstraZeneca n=990
NCT06283966 RECRUITING
A Study Evaluating the Efficacy of Budesonide, Glycopyrronium and Formoterol Fumarate Metered Dosed Inhaler on Cardiopulmonary Outcomes in Chronic Obstructive Pulmonary Disease
AstraZeneca n=5,000
NCT07190209 RECRUITING
Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD) Characterized by an Eosinophilic Phenotype
Sanofi n=942
NCT05878769 RECRUITING
A Study to Evaluate the Long-Term Safety of Astegolimab in Participants With Chronic Obstructive Pulmonary Disease (COPD)
Hoffmann-La Roche n=2,000
NCT07190222 RECRUITING
Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD), Characterized by an Eosinophilic Phenotype
Sanofi n=942
NCT05595642 RECRUITING
A Study to Evaluate Astegolimab in Participants With Chronic Obstructive Pulmonary Disease
Hoffmann-La Roche n=1,290
NCT07363694 NOT YET RECRUITING
A Study to Learn About the Study Medicine Called PF-07275315 in People With Moderate to Severe Chronic Obstructive Pulmonary Disease
Pfizer n=1,156
NCT05166889 ACTIVE NOT RECRUITING
Efficacy and Safety of Tozorakimab in Symptomatic Chronic Obstructive Pulmonary Disease With a History of Exacerbations
AstraZeneca n=1,132
NCT05158387 ACTIVE NOT RECRUITING
Efficacy and Safety of Tozorakimab in Symptomatic Chronic Obstructive Pulmonary Disease With a History of Exacerbations.
AstraZeneca n=1,172
NCT05742802 ACTIVE NOT RECRUITING
Long-term Efficacy and Safety of Tozorakimab in Participants With Chronic Obstructive Pulmonary Disease With a History of Exacerbations (PROSPERO).
AstraZeneca n=1,711
NCT07330310 NOT YET RECRUITING
A Phase 3 Trial of JKN2401 Injection in COPD
Joincare Pharmaceutical Group Industry Co., Ltd n=888
NCT05844462 RECRUITING
Tadalafil for Severe Pulmonary Hypertension Due to Chronic Obstructive Pulmonary Disease
Assistance Publique - Hôpitaux de Paris n=200
NCT06067828 ACTIVE NOT RECRUITING
A Study to Evaluate the Effect of Budesonide, Glycopyrronium, Formoterol Fumarate (BGF) Metered Dose Inhaler (MDI), Budesonide and Formoterol Fumarate (BFF) MDI and Placebo MDI on Exercise Parameters in Participants With Chronic Obstructive Pulmonary Disease (COPD).
AstraZeneca n=171
NCT06040086 ACTIVE NOT RECRUITING
Efficacy and Safety of Tozorakimab in Symptomatic Chronic Obstructive Pulmonary Disease With a History of Exacerbations
AstraZeneca n=1,454
NCT04004117 RECRUITING
Effect of Sublingual Fentanyl on Breathlessness in COPD
McGill University Health Centre/Research Institute of the McGill University Health Centre n=40
NCT07177339 RECRUITING
eValuating the Efficacy and Safety of InitiatinG depemokImab earLy therApy iN Chronic Obstructive Pulmonary Disorder (COPD) With Type 2 Inflammation
GlaxoSmithKline n=1,196
NCT07039669 RECRUITING
Evaluation of 611 in Chinese Adults Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease
Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. n=594
NCT06376994 RECRUITING
Multi-Center Clean Air Randomized Controlled Trial in COPD
JHSPH Center for Clinical Trials n=770
NCT06959095 RECRUITING
Depemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA -1)
GlaxoSmithKline n=981
NCT07147946 NOT YET RECRUITING
Evaluation of the Clinical Trial of Inhaled TQC3721 Suspension in Patients With Moderate-to-Severe Chronic Obstructive Pulmonary Disease
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. n=666
NCT06961214 RECRUITING
Depemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA-2)
GlaxoSmithKline n=960
NCT07047092 NOT YET RECRUITING
Non-invasive Ventilation or CPAP in OSA-COPD Following Admission for an Acute Hypercapnic Respiratory Failure
Assistance Publique - Hôpitaux de Paris n=386
NCT06208306 ACTIVE NOT RECRUITING
A Study to Investigate Long-term Safety and Tolerability of Itepekimab in Participants With COPD
Sanofi n=700
NCT06999343 NOT YET RECRUITING
Exploring the Anti-ageing Effects of Metformin in COPD
Fundación Instituto de Investigación Sanitaria de Navarra n=212
NCT06474039 RECRUITING
The Efficacy of Fluticasone Furoate/Vilanterol/Umeclidinium Compared With Vilanterol/Umeclidinium in Reducing Air Trapping and Airway and Blood Cytokine Levels in COPD
Mahidol University n=50
NCT05138250 ACTIVE NOT RECRUITING
A Pilot Study of the Use of 129Xe and 1H MRI to Measure the Modulation of Eosinophil-Related Inflammation by Mepolizumab In COPD
Sheffield Teaching Hospitals NHS Foundation Trust n=32
NCT05265299 RECRUITING
Trial to Determine Effective Aspirin Dose in COPD
Johns Hopkins University n=48
NCT02984124 ACTIVE NOT RECRUITING
Communication During Hospitalization About Resuscitation Trial
University of Vermont n=182
NCT06234345 NOT YET RECRUITING
Study of Fluticasone/Formoterol/Glycopyrronium for the Treatment Chronic Obstructive Pulmonary Disease (TRIPLAR)
Eurofarma Laboratorios S.A. n=1,252
NCT06347536 RECRUITING
Supported Rescue Packs Post-discharge in Chronic Obstructive Pulmonary Disease
Guy's and St Thomas' NHS Foundation Trust n=1,400
NCT06785337 RECRUITING
"The Effect of Inhaled Nitroglycerin for COPD Patients
Beni-Suef University n=40
NCT06643078 RECRUITING
A Study to Evaluate the Safety and Efficacy of HL231 Solution for Inhalation in Patients with COPD
Haisco Pharmaceutical Group Co., Ltd. n=474
NCT06547333 NOT YET RECRUITING
A Study of CM310 in Subjects With Moderate to Severe Chronic Obstructive Pulmonary Disease
CSPC ZhongQi Pharmaceutical Technology Co., Ltd. n=884
NCT06212765 NOT YET RECRUITING
Oral Citrulline Supplementation in COPD Patients With Malnutrition
University Hospital, Grenoble n=60
NCT04018729 RECRUITING
Cell Therapy Associated With Endobronchial Valve
Hospital de Clinicas de Porto Alegre n=34
NCT04636814 TERMINATED
A 52-week, Placebo- and Active- Controlled (Roflumilast, Daliresp® 500µg) Study to Evaluate the Efficacy and Safety of Two Doses of CHF6001 DPI (Tanimilast) as add-on to Maintenance Triple Therapy in Subjects With COPD and Chronic Bronchitis. (PILLAR)
Chiesi Farmaceutici S.p.A. n=3,973
NCT04320342 COMPLETED
A Study Comparing Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination CHF 5993 With the Fixed Dose Dual Combination CHF 1535 in Subjects With COPD
Chiesi Farmaceutici S.p.A. n=3,433
NCT04636801 TERMINATED
A 52-week, Placebo-controlled Study to Evaluate the Efficacy and Safety of 2 Doses of CHF6001 DPI (Tanimilast), as add-on to Maintenance Triple Therapy in Subjects With COPD and Chronic Bronchitis (PILASTER)
Chiesi Farmaceutici S.p.A. n=4,710
NCT03794583 TERMINATED
Inhaled Treprostinil in Participants With Pulmonary Hypertension Due to Chronic Obstructive Pulmonary Disease (PH-COPD)
United Therapeutics n=41
NCT04751487 COMPLETED
Study to Assess the Efficacy, Safety, and Tolerability of SAR440340/REGN3500/Itepekimab in Chronic Obstructive Pulmonary Disease (COPD)
Sanofi n=1,239
NCT04701983 COMPLETED
Study to Assess the Efficacy, Safety, and Tolerability of SAR440340/REGN3500/Itepekimab in Chronic Obstructive Pulmonary Disease (COPD)
Sanofi n=1,127
NCT05573464 COMPLETED
A Study to Assess the Safety of Budesonide/Glycopyrronium/Formoterol Fumarate With a Next-Generation Propellant in Participants With Moderate to Very Severe Chronic Obstructive Pulmonary Disease
AstraZeneca n=559
NCT02683668 COMPLETED
Airway Effects of Tiotropium in Patients With COPD
Imperial College London n=44
NCT06075095 COMPLETED
A Study to Investigate the Effect on Lung Function of an Approved COPD Treatment (BGF, With HFA Propellant) Compared to BGF Formulated With a Next-Generation Propellant in Participants 40 to 80 Years of Age With COPD
AstraZeneca n=297
NCT04053634 COMPLETED
Efficacy and Safety of Benralizumab in Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) With a History of Frequent Exacerbations
AstraZeneca n=689
NCT04133909 COMPLETED
Mepolizumab as Add-on Treatment IN Participants With COPD Characterized by Frequent Exacerbations and Eosinophil Level
GlaxoSmithKline n=806
NCT05743075 COMPLETED
A Study to Evaluate the Efficacy and Safety of Ensifentrine for 24 Weeks in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease
Nuance Pharma (shanghai) Co., Ltd n=526
NCT04456673 COMPLETED
Pivotal Study to Assess the Efficacy, Safety and Tolerability of Dupilumab in Patients With Moderate to Severe COPD With Type 2 Inflammation
Sanofi n=935
NCT03022097 COMPLETED
Study to Assess Efficacy and Safety of Aclidinium Bromide and Aclidinium Bromide/Formoterol Fumarate in Stabile COPD Patients
AstraZeneca n=1,625
NCT03956888 COMPLETED
The Anti-oxidant Effects of N-Acetylcysteine in Chronic Obstructive Pulmonary Disease (COPD)
Siriraj Hospital n=35
NCT02887521 TERMINATED
Pulmonary Rehabilitation Before Lung Cancer Resection
Alliance for Clinical Trials in Oncology n=9
NCT03888131 COMPLETED
Foster® pMDI (CHF 1535) Versus Symbicort® Turbohaler in COPD Patient
Chiesi Farmaceutici S.p.A. n=750
NCT03984188 COMPLETED
Effectiveness of Low-Dose Theophylline for the Management of Biomass-Associated COPD
University of Miami n=100
NCT04517500 COMPLETED
A Home-based Module to Promote Mindful Breathing Awareness for COPD Patients
Mayo Clinic n=99
NCT05046795 COMPLETED
Revefenacin in Chinese Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease(COPD)
Mylan Pharma UK Ltd. n=258
NCT04075331 COMPLETED
Mepolizumab for COPD Hospital Eosinophilic Admissions Pragmatic Trial
University of Leicester n=238
NCT03930732 COMPLETED
Pivotal Study to Assess the Efficacy, Safety and Tolerability of Dupilumab in Patients With Moderate-to-severe COPD With Type 2 Inflammation
Sanofi n=939
NCT05986591 COMPLETED
Bioequivalence Study of Tiotropium 18 μg Inhalation Powder, Hard Capsule With Spiriva®Handihaler® 18 μg Inhalation Powder, Hard Capsule in Patients With Chronic Obstructive Pulmonary Disease (COPD)
Xiromed LLC n=335
NCT03496623 TERMINATED
A Phase 3 Adaptive Study to Evaluate the Safety and Efficacy of Inhaled Treprostinil in Participants With Pulmonary Hypertension (PH) Due to Chronic Obstructive Pulmonary Disease (COPD)
United Therapeutics n=188
NCT04535986 COMPLETED
A Phase 3 Clinical Trial to Evaluate the Safety and Efficacy of Ensifentrine in Patients With COPD
Verona Pharma plc n=763
NCT04542057 COMPLETED
A Phase 3 Trial to Evaluate the Safety and Efficacy of Ensifentrine in Patients With COPD
Verona Pharma plc n=790
NCT05927155 COMPLETED
Effects of Acute Long-acting Bronchodilation on Oxygenation and Peripheral Ventilation in COPD
Erasme University Hospital n=30
NCT02867761 COMPLETED
RETHINC: REdefining THerapy In Early COPD for the Pulmonary Trials Cooperative
University of Michigan n=780
NCT05161156 COMPLETED
Bioequivalence Study of Tiotropium Bromide Inhalation Powder
Phargentis SA n=306
NCT04078126 COMPLETED
Study Comparing Dual Combination of Product (Budesonide and Formoterol) Given Via Two Different Inhalers. To See Which One Results in the Best Effect on Breathing.
AstraZeneca n=35
NCT02512510 COMPLETED
Efficacy Study of Nebulized TD-4208 for Chronic Obstructive Pulmonary Disease (COPD)
Mylan Inc. n=611
NCT02518139 COMPLETED
A 52-Week Parallel Group Safety Study of TD-4208 in Chronic Obstructive Pulmonary Disease (COPD)
Mylan Inc. n=1,060
NCT02459080 COMPLETED
Efficacy Study of Nebulized TD-4208 for Chronic Obstructive Pulmonary Disease (COPD)
Mylan Inc. n=619
NCT03573817 COMPLETED
A 42-day Parallel Group Safety Study of Revefenacin and Formoterol, Administered in Sequence and as a Combination, in Participants With COPD
Mylan Inc. n=122
NCT03674320 WITHDRAWN
Cycled Testosterone Administration During Pulmonary Rehabilitation in Early Stage COPD
The University of Texas Medical Branch, Galveston
NCT03256695 COMPLETED
Evaluate the Relationship Between Use of Albuterol Multidose Dry Powder Inhaler With an eModule (eMDPI) and Exacerbations in Participants With Chronic Obstructive Pulmonary Disease (COPD)
Teva Branded Pharmaceutical Products R&D, Inc. n=405
NCT02579850 COMPLETED
2-arm Parallel Group Study of Fixed Combination of CHF 5993 vs Ultibro® in COPD Patients
Chiesi Farmaceutici S.p.A. n=1,532
NCT02467452 COMPLETED
Non Inferiority of Fixed Combination of Beclomethasone Dipropionate (BDP) + Formoterol Fumarate (FF) + Glycopyrronium Bromide (GB) Versus Combination of Fluticasone Furoate (FlF)/Vilanterol (VI) + Tiotropium Bromide in Chronic Obstructive Pulmonary Disease (COPD)
Chiesi Farmaceutici S.p.A. n=1,479
NCT04446637 WITHDRAWN
Acute Bronchodilator Effects of Ipratropium/Levosalbutamol 20/50 mcg Fixed Dose Combination vs Salbutamol 100 mcg Inhaler Plus Ipratropium 20 mcg Inhalation Aerosol Free Combination in Patients With Stable COPD
Neutec Ar-Ge San ve Tic A.Ş
NCT02722304 TERMINATED
Stage 1 Study of ARALAST NP and GLASSIA in A1PI Deficiency
Baxalta now part of Shire n=7
NCT04879030 COMPLETED
Combination Antibiotic Therapy Compared to Monotherapy in the Treatment of Acute COPD
Haiphong University of Medicine and Pharmacy n=170
NCT03137992 COMPLETED
Clinical Endpoint Bioequivalence Study of Test and Reference Inhalation Products in Patients With COPD With Device Robustness
Lupin, Inc. n=377
NCT03197818 COMPLETED
Active Controlled Trial of CHF5993 Pressurized Metered-dose Inhaler ( pMDI) vs Symbicort®Turbuhaler® in Patients With Chronic Obstructive Pulmonary Disease ( COPD)
Chiesi Farmaceutici S.p.A. n=990
NCT02536508 COMPLETED
Study to Assess the Safety and Tolerability of PT010, PT009 and PT003 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease
Pearl Therapeutics, Inc. n=627
NCT03836677 COMPLETED
A Study to Evaluate the Effects of BGF and GFF on Specific Image Based Airway Volumes and Resistance in Subjects With Moderate to Severe COPD
AstraZeneca n=23
NCT02465567 COMPLETED
Study to Assess the Efficacy and Safety of PT010 Relative to PT003 and PT009 in Subjects With Moderate to Very Severe COPD (Ethos)
Pearl Therapeutics, Inc. n=8,588
NCT02587351 TERMINATED
Beta-Blockers for the Prevention of Acute Exacerbations of Chronic Obstructive Pulmonary Disease
University of Minnesota n=532
NCT03324607 COMPLETED
Effects of Bevespi on Ventilation and Gas Exchange Abnormalities in COPD Assessed by 129Xe MRI
Bastiaan Driehuys n=20
NCT03379233 TERMINATED
A Randomized Study to Evaluate the Effect of Reminder Notifications and Motivational/Adaptive Messaging on Treatment Adherence
Novartis Pharmaceuticals n=7
NCT02497001 COMPLETED
A Randomized, Double-Blind, Parallel-Group, 24-Week, Chronic-Dosing, Multi-Center Study to Assess the Efficacy and Safety of PT010, PT003, and PT009 Compared With Symbicort® Turbuhaler® (Kronos)
Pearl Therapeutics, Inc. n=1,902
NCT02067780 COMPLETED
Short Antibiotic Treatment Versus Duration Guided by Markers of Inflammation in the Treatment of AECOPD
University of Monastir n=310
NCT04479930 COMPLETED
Effects of an mHealth Web-Based Platform (HappyAir) on Adherence to a Maintenance Program After Pulmonary Rehabilitation in Patients With Chronic Obstructive Pulmonary Disease
CEU San Pablo University n=44
NCT02184611 COMPLETED
A 24 Week Efficacy Study of Inhaled Umeclidinium (UMEC) in Patients of Chronic Obstructive Pulmonary Disease (COPD) Using a Novel Dry Powder Inhaler (NDPI)
GlaxoSmithKline n=308
NCT04361552 WITHDRAWN
Tocilizumab for the Treatment of Cytokine Release Syndrome in Patients With COVID-19 (SARS-CoV-2 Infection)
Emory University
NCT03262012 COMPLETED
Study to Assess the Safety and Efficacy of PT010, PT003, and PT009 in Japanese Subjects With COPD Compared With Symbicort® Turbohaler®
Pearl Therapeutics, Inc. n=416
NCT04122547 COMPLETED
Efficacy of Roflumilast on Exacerbations in Patients With Non-cystic Fibrosis Bronchiectasis
Prince of Songkla University n=40
NCT02685293 TERMINATED
Study to Evaluate the Treatment Effect of PT003 on Cardiovascular Hemodynamics in Subjects With Moderate to Severe COPD
Pearl Therapeutics, Inc. n=4
NCT02937584 COMPLETED
A Study to Assess the Effects of PT001 and PT005 MDI on Specific Image Based Parameters in Subjects With Moderate to Severe COPD
Pearl Therapeutics, Inc. n=23
NCT02729051 COMPLETED
Comparative Study of Fluticasone Furoate(FF)/Umeclidinium Bromide (UMEC)/ Vilanterol (VI) Closed Therapy Versus FF/VI Plus UMEC Open Therapy in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
GlaxoSmithKline n=1,055
NCT02629965 COMPLETED
Comparing the Efficacy of Tiotropium + Olodaterol Fixed Dose Combination (FDC) Over Tiotropium in Improvement of Lung Hyperinflation, Exercise Capacity and Physical Activity in Japanese COPD Patients
Boehringer Ingelheim n=184
NCT03162055 COMPLETED
Efficacy and Safety of Glycopyrronium/Formoterol Fumarate Fixed-dose Combination Relative to Umeclidinium/Vilanterol Fixed-dose Combination Over 24 Weeks in Patients With Moderate to Very Severe Chronic Obstructive Pulmonary Disease
AstraZeneca n=1,119
NCT02888444 TERMINATED
Smoking Relapse Prevention Among COPD Ex-smokers
University of Auckland, New Zealand n=8
NCT02643082 COMPLETED
A Study to Assess the Effects of PT003 and Placebo MDI on Specific Image Based Airway Volumes and Resistance in Subjects With Moderate to Severe COPD
Pearl Therapeutics, Inc. n=20
NCT02343458 COMPLETED
Study to Assess the Efficacy and Safety of PT003, PT005, and PT001 in Subjects With Moderate to Very Severe COPD
Pearl Therapeutics, Inc. n=1,756
NCT03081247 WITHDRAWN
To Assess the Efficacy and Safety of PT010 Compared to PT009 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease
Pearl Therapeutics, Inc.
NCT02347085 COMPLETED
24-hour Lung Function in Subjects With Moderate to Very Severe COPD After Treatment With PT003 and Placebo MDI
Pearl Therapeutics, Inc. n=43
NCT02345161 COMPLETED
A Comparison Study Between the Fixed Dose Triple Combination of Fluticasone Furoate/ Umeclidinium/ Vilanterol Trifenatate (FF/UMEC/VI) With Budesonide/Formoterol in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
GlaxoSmithKline n=1,811
NCT02296138 COMPLETED
Comparing the Efficacy of Tiotropium + Olodaterol (5/5 µg) Fixed Dose Combination (FDC) Over Tiotropium 5µg in Reducing Moderate to Severe Exacerbations in Patients With Severe to Very Severe Chronic Obstructive Pulmonary Disease.
Boehringer Ingelheim n=7,903
NCT02487498 COMPLETED
Efficacy and Safety Study of Indacaterol Maleate/Glycopyrronium Bromide in Chronic Obstructive Pulmonary Disease (COPD) Patients.
Novartis Pharmaceuticals n=355
NCT02347761 COMPLETED
Efficacy and Safety Trial of 12 Weeks of Treatment With Nebulized SUN-101 in Patients With COPD
Sunovion Respiratory Development Inc. n=653
NCT02347774 COMPLETED
Efficacy and Safety Trial of 12 Weeks of Treatment With Nebulized SUN-101 in Patients With COPD (GOLDEN-4)
Sunovion Respiratory Development Inc. n=641
NCT02487446 COMPLETED
Efficacy and Safety Study of QVA149 in COPD Patients
Novartis Pharmaceuticals n=357
NCT02347072 COMPLETED
24-hour Lung Function in Subjects With Moderate to Very Severe COPD After Treatment With PT003, Open-Label Spiriva® Respimat® as an Active Control, and Placebo
Pearl Therapeutics, Inc. n=80
NCT02454959 COMPLETED
Crossover Study to Assess the Efficacy of PT003 With and Without a Valved Holding Chamber in Subjects With Moderate to Severe COPD
Pearl Therapeutics, Inc. n=80
NCT02594722 COMPLETED
Metabolism and Oxygen Consumption During Functional Electrical Stimulation Cycling in COPD
University Hospital, Rouen n=25
NCT02731846 WITHDRAWN
A Study Comparing the Closed Triple Therapy, Open Triple Therapy and a Dual Therapy for Effect on Lung Function in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
GlaxoSmithKline
NCT02455362 WITHDRAWN
Opioids for Refractory Breathlessness in Chronic Obstructive Pulmonary Disease
Flinders University
Data: ClinicalTrials.gov