Tiotropium
Regulatory milestones approvals, filings & regulatory actions · 4 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Approved | EU (EMA) | Trimbow | — | 2017-07-17 | europa.eu ↗ |
| Label expansion | US (FDA) | SPIRIVA RESPIMAT | — | 2017-02-15 | fda.gov ↗ |
| Label expansion | US (FDA) | SPIRIVA | — | 2009-12-17 | fda.gov ↗ |
| Approved | US (FDA) | SPIRIVA | — | 2004-01-30 | fda.gov ↗ |
Trials 193 · started per year
Also used as a comparator or background therapy in 134 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 19 trials | ||||||
| Phase 1 | NCT06254664 Background | Oct 2022 → Jul 2023 | chronic obstructive pulmonary disease | Xiromed LLC | Completed | No outcome recorded |
| Phase 1 | NCT04850144 Comparator | Apr → Oct 2021 | — | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 1 | NCT03400241 Comparator | Feb → Apr 2018 | — | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 1 | NCT03097380 Comparator | Apr → Dec 2017 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT02059434 Comparator | Sep 2013 → Oct 2014 | asthma, chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT01355991 Comparator | Aug 2011 → Mar 2016 | spinal cord injury | James J. Peters Veterans Affairs Medical Center | Unknown | No outcome recorded |
| Phase 1 | NCT02231177 Comparator | Jun → Nov 2008 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1 | NCT00568503 Comparator | Oct 2007 → Feb 2008 | chronic obstructive pulmonary disease | Novartis | Completed | No outcome recorded |
| Phase 1 | NCT00532350 Comparator | Jul 2007 → Jan 2008 | chronic obstructive pulmonary disease | Novartis | Completed | No outcome recorded |
| Phase 1/22 trials | ||||||
| Phase 1/2 | NCT01176903 Comparator | Aug → Nov 2010 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 1/2 | NCT00871182 Comparator | Mar → Sep 2009 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 225 trials | ||||||
| Phase 2 | NCT05838703 Comparator | May 2023 → May 2024 | chronic obstructive pulmonary disease | Duke University | Withdrawn | No outcome recorded |
| Phase 2 | NCT03937479 Background | May → Nov 2019 | chronic obstructive pulmonary disease | Verona Pharma, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT03673670 Background | Jul → Nov 2018 | chronic obstructive pulmonary disease | Verona Pharma, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT03084796 Comparator | Jul 2017 → May 2018 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT03118765 Comparator | Mar → Jul 2017 | chronic obstructive pulmonary disease | Glenmark Specialty S.A. | Completed | No outcome recorded |
| Phase 2 | NCT03028142 Background | Jan → Aug 2017 | chronic obstructive pulmonary disease | Verona Pharma, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT02382510 Comparator | Apr 2015 → Mar 2016 | asthma | Theron Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01708057 Comparator | Oct → Dec 2012 | chronic obstructive pulmonary disease | AstraZeneca | Terminated | No outcome recorded |
| Phase 2 | NCT01543919 Background | Apr 2012 → Sep 2013 | chronic obstructive pulmonary disease | Pfizer | Completed | No outcome recorded |
| Phase 2 | NCT01587079 Comparator | Apr → Sep 2012 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01566773 Comparator | Mar → Aug 2012 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01498081 Comparator | Mar → Oct 2012 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT01426009 Comparator | Aug → Dec 2011 | chronic obstructive pulmonary disease | Sunovion Respiratory Development Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01372410 Comparator | Jul → Oct 2011 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT01085045 Comparator | Mar → Nov 2010 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01068613 Comparator | Jan → Aug 2010 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT00950807 Comparator | Sep 2009 → Mar 2010 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT00939211 Comparator | Jun → Nov 2009 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT00868231 Comparator | Mar → Jul 2009 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT00720499 Background | Jul 2008 → Feb 2009 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2 | NCT00535366 Background | Oct 2007 → Sep 2008 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2 | NCT00501852 Comparator | Jul → Dec 2007 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT00515502 Comparator | Jun → Nov 2007 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT02242279 Comparator | Jun → Dec 2004 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2 | NCT02242240 Background | Mar → Dec 2001 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2/31 trial | ||||||
| Phase 2/3 | NCT00463567 Comparator | Apr 2007 → Aug 2008 | chronic obstructive pulmonary disease | Novartis | Completed | No outcome recorded |
| Phase 351 trials | ||||||
| Phase 3 | NCT04208581 Background | Oct 2019 → Dec 2021 | chronic obstructive pulmonary disease, respiratory failure | Peking University People's Hospital | Unknown | No outcome recorded |
| Phase 3 | NCT03976713 Background | Jun 2019 → Jun 2020 | chronic obstructive pulmonary disease | Henan University of Traditional Chinese Medicine | Unknown | No outcome recorded |
| Phase 3 | NCT03376932 Comparator | Jan 2019 → Feb 2021 | asthma | GlaxoSmithKline | Withdrawn | No outcome recorded |
| Phase 3 | NCT03745261 Background | Jun 2018 → Dec 2019 | chronic obstructive pulmonary disease | Henan University of Traditional Chinese Medicine | Unknown | No outcome recorded |
| Phase 3 | NCT03158311 Comparator | Feb 2018 → Jul 2019 | asthma | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT02676089 Comparator | Apr 2016 → May 2018 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 3 | NCT02629965 Comparator | Feb 2016 → Mar 2017 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02518139 Comparator | Sep 2015 → Jun 2017 | chronic obstructive pulmonary disease | Mylan Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02467452 Comparator | May 2015 → Jan 2017 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 3 | NCT02347072 Comparator | Feb → Aug 2015 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02296138 Comparator | Jan 2015 → Mar 2017 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02257385 Comparator | Oct 2014 → May 2015 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02276222 Comparator | Oct 2014 → Feb 2016 | chronic obstructive pulmonary disease | Sunovion Respiratory Development Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01899742 Comparator | Sep 2014 → Jul 2015 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02207829 Comparator | Sep 2014 → May 2015 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02165826 Background | May 2014 → Sep 2015 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT01837927 Comparator | Apr 2014 → Apr 2016 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Withdrawn | No outcome recorded |
| Phase 3 | NCT01911364 Comparator | Jan 2014 → Mar 2016 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 3 | NCT01970878 Comparator | Nov 2013 → Mar 2015 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01964352 Comparator | Nov 2013 → Oct 2014 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT01854645 Comparator | May 2013 → Feb 2015 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01777334 Comparator | Jan → Sep 2013 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01610037 Comparator | Oct 2012 → Feb 2015 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01694771 Background | Sep 2012 → Aug 2013 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT01696058 Background | Sep 2012 → Oct 2013 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT01613326 Comparator | Jun 2012 → Jan 2013 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01574651 Comparator | May 2012 → Apr 2013 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01627327 Comparator | Apr → Dec 2012 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01513460 Comparator | Apr 2012 → Dec 2013 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01533922 Comparator | Mar 2012 → Nov 2013 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT01462929 Comparator | Nov 2011 → Mar 2012 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT01490125 Comparator | Oct 2011 → Aug 2012 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01395888 Comparator | Jun 2011 → Aug 2012 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01316900 Comparator | Mar 2011 → Apr 2012 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01316913 Comparator | Mar 2011 → Apr 2012 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01294787 Comparator | Feb → Nov 2011 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01285492 Comparator | Jan 2011 → Sep 2012 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01202188 Comparator | Sep 2010 → Feb 2012 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01126437 Comparator | May 2010 → May 2013 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT01120691 Comparator | Apr 2010 → Jul 2012 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01040689 Comparator | Jan 2010 → Jan 2011 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT01040728 Comparator | Jan 2010 → Jan 2011 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00929110 Comparator | Jun 2009 → Apr 2011 | chronic obstructive pulmonary disease | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00900731 Comparator | Jun 2009 → Mar 2010 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT00877383 Background | Apr 2009 → Feb 2010 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT00845728 Comparator | Mar 2009 → Jul 2012 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT00846586 Background | Mar 2009 → Mar 2010 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT00662740 Comparator | Apr → Nov 2008 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Terminated | No outcome recorded |
| Phase 3 | NCT00435760 Comparator | Feb → Aug 2007 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00308191 Background | Apr → May 2006 | chronic obstructive pulmonary disease | Dey | Completed | No outcome recorded |
| Phase 3 | NCT00274066 Background | Oct 2002 → Sep 2003 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 437 trials | ||||||
| Phase 4 | NCT06282861 Comparator | Feb 2024 → Jan 2025 | chronic obstructive pulmonary disease | Fundacio Privada Mon Clinic Barcelona | Terminated | No outcome recorded |
| Phase 4 | NCT05113615 Comparator | Dec 2021 → May 2022 | asthma | University of Saskatchewan | Completed | No outcome recorded |
| Phase 4 | NCT04061161 Comparator | Aug 2019 → Dec 2023 | chronic obstructive pulmonary disease | University Medical Center Groningen | Completed | No outcome recorded |
| Phase 4 | NCT03395002 Comparator | Mar 2018 → Apr 2020 | chronic obstructive pulmonary disease | Neutec Ar-Ge San ve Tic A.Ş | Completed | No outcome recorded |
| Phase 4 | NCT02546297 Comparator | Sep 2017 → Sep 2020 | bronchiectasis | Shanghai Pulmonary Hospital, Shanghai, China | Unknown | No outcome recorded |
| Phase 4 | NCT03275116 Comparator | Jul 2017 → Apr 2020 | chronic obstructive pulmonary disease | Maastricht University Medical Center | Unknown | No outcome recorded |
| Phase 4 | NCT03152149 Comparator | Jun 2017 → Nov 2019 | chronic obstructive pulmonary disease | University of Dundee | Completed | No outcome recorded |
| Phase 4 | NCT02853123 Comparator | Sep 2016 → Jul 2017 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT02988869 Comparator | Aug 2016 → Aug 2017 | chronic obstructive pulmonary disease | Neutec Ar-Ge San ve Tic A.Ş | Completed | No outcome recorded |
| Phase 4 | NCT02683109 Comparator | Mar 2016 → Jan 2017 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT02603393 Comparator | Nov 2015 → Jul 2017 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT02275481 Comparator | Nov 2014 → Sep 2016 | chronic obstructive pulmonary disease | Sumitomo Pharma America, Inc. | Terminated | No outcome recorded |
| Phase 4 | NCT02039050 Comparator | Feb 2014 → Jul 2015 | chronic obstructive pulmonary disease | University of Dundee | Completed | No outcome recorded |
| Phase 4 | NCT02473237 Comparator | Apr 2013 → Jun 2015 | chronic obstructive pulmonary disease | National Institute of Respiratory Diseases, Mexico | Completed | No outcome recorded |
| Phase 4 | NCT01727024 Comparator | Apr 2013 → Nov 2015 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT02566031 Comparator | Mar 2013 → Jun 2018 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT01751113 Comparator | Feb → Nov 2013 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT01715311 Comparator | Nov 2012 → Sep 2013 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Withdrawn | No outcome recorded |
| Phase 4 | NCT05506865 Comparator | Sep 2012 → Jan 2016 | chronic obstructive pulmonary disease | National Institute of Respiratory Diseases, Mexico | Completed | No outcome recorded |
| Phase 4 | NCT01663987 Comparator | Aug 2012 → May 2014 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT01662986 Comparator | Aug 2012 → Apr 2014 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT01455129 Comparator | Nov 2011 → Aug 2016 | chronic obstructive pulmonary disease | The First Affiliated Hospital of Guangzhou Medical University | Completed | No outcome recorded |
| Phase 4 | NCT01466712 Background | Nov 2011 → Dec 2014 | pulmonary emphysema | KU Leuven | Unknown | No outcome recorded |
| Phase 4 | NCT01437748 Comparator | Aug 2011 → Sep 2014 | chronic obstructive pulmonary disease | University of Milan | Completed | No outcome recorded |
| Phase 4 | NCT01124422 Background | Jul 2010 → May 2011 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT01072396 Comparator | Feb 2010 → Nov 2011 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00864812 Comparator | Mar 2009 → Mar 2010 | chronic obstructive pulmonary disease | The Korean Academy of Tuberculosis and Respiratory Diseases | Completed | No outcome recorded |
| Phase 4 | NCT00975195 Background | Feb 2009 → Jul 2013 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00784550 Comparator | Dec 2008 → Dec 2009 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT00563381 Comparator | Jan 2008 → Apr 2010 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00546234 Comparator | Nov 2007 → Jan 2014 | asthma | University of Alberta | Withdrawn | No outcome recorded |
| Phase 4 | NCT00496470 Comparator | May 2007 → Jun 2008 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT00424528 Comparator | Dec 2006 → Oct 2007 | bronchitis, pulmonary emphysema | Sumitomo Pharma America, Inc. | Completed | No outcome recorded |
| Phase 4 | NCT00996697 Comparator | Oct 2006 → Sep 2008 | chronic obstructive pulmonary disease | Brian J Lipworth | Completed | No outcome recorded |
| Phase 4 | NCT00412204 Comparator | Jun 2006 → Apr 2009 | chronic obstructive pulmonary disease | McMaster University | Completed | No outcome recorded |
| Phase 4 | NCT00394485 Background | May 2006 → Apr 2008 | chronic obstructive pulmonary disease | Otsuka Pharmaceutical Co., Ltd. | Terminated | No outcome recorded |
| Phase 4 | NCT01307189 Comparator | Apr 2005 → Aug 2010 | chronic obstructive pulmonary disease | Laval University | Completed | No outcome recorded |
| Phase not applicable9 trials | ||||||
| — | NCT07058259 Background | Nov 2024 → Jun 2025 overdue | chronic obstructive pulmonary disease | Istanbul Medeniyet University | Active not recruiting | No outcome recorded |
| — | NCT06609941 Background | Jun 2024 → Jan 2025 overdue | asthma | Foundation University Islamabad | Recruiting | No outcome recorded |
| — | NCT05295355 Background | Jan 2021 → Sep 2024 | chronic obstructive pulmonary disease | Guangzhou Institute of Respiratory Disease | Unknown | No outcome recorded |
| — | NCT03504527 Comparator | May → Nov 2018 | bronchial disorder | Huashan Hospital | Unknown | No outcome recorded |
| — | NCT03083067 Background | Mar 2017 → Mar 2022 | chronic obstructive pulmonary disease | Peking University First Hospital | Completed | No outcome recorded |
| — | NCT02790047 Background | Oct 2016 → Jan 2018 | chronic obstructive pulmonary disease | Khon Kaen University | Unknown | No outcome recorded |
| — | NCT02257463 Comparator | Oct 2011 → Apr 2014 | chronic obstructive pulmonary disease | Mansoura University | Completed | No outcome recorded |
| — | NCT02331940 Comparator | Mar 2010 → Dec 2013 | chronic obstructive pulmonary disease | University of Crete | Completed | No outcome recorded |
| — | NCT00981851 Comparator | Sep 2009 → May 2011 | cardiovascular disorder, chronic obstructive pulmonary disease | Radboud University Medical Center | Completed | No outcome recorded |
Evidence & citations 24 cited values
Every value below carries the sentence it was read from. 341 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Tiotropium | “This pilot study was designed to evaluate the pharmacokinetic characteristics of fluticasone, salmeterol, and tiotropium after co-administration of HCP 0910 (Seretide 250...” NCT02441114 ↗278“The investigators will compare the reduction in Borg dyspnea score during the 3-min constant rate shuttle walking test after 3 weeks of indacaterol 110 µg/Glycopyrronium 50 µg...” NCT02567214 ↗ “The primary objective of this study is to evaluate the efficacy and safety of orally inhaled tiotropium and olodaterol as both a fixed dose combination and a free combination...” NCT02030535 ↗ “Assessment In a Real World Setting of the Effect of Inhaled Steroid-based Triple Therapy Versus the Combination of Tiotropium and Olodaterol on Reducing Chronic Obstructive...” NCT03265145 ↗ “Tiotropium, a once-daily long-acting anticholinergic agent, has been shown to be an efficacious and safe add-on treatment for adults with symptomatic asthma, despite treatment...” PMID 25081651 ↗ Jul 2014 “patients were randomized to receive either tiotropium 5 μg or a fixed-dose combination of tiotropium 5 μg with olodaterol 2 μg, 5 μg, or 10 μg, delivered once daily via the...” PMID 30843141 ↗ Mar 2019 “Each actuation from the RESPIMAT inhaler delivers 3.124 mcg tiotropium bromide monohydrate (equivalent to 2.5 mcg tiotropium) and 2.736 mcg olodaterol hydrochloride (equivalent...” NCT02799784 ↗ “Examples of LABA containing products are: Formoterol, Salmeterol, Indacaterol, Formoterol/Budesonide, Salmeterol/Fluticasone, Treatment including lon-acting anticholinergics:...” NCT02165826 ↗ “An Open-label Positron Emission Tomography Phase I Study to Determine Muscarinic Receptor Occupancy in the Lungs in Healthy Volunteers After Inhalation of Single Dose of...” NCT03097380 ↗ “Tiotropium Bromide Powder for Inhalation (Spiriva®, Boehringer Ingelheim International GmbH), 18 μg/capsule, 10 capsule, 18 μg each time, once daily for 12 weeks.” NCT03169504 ↗ “Inhalation of 4 puffs of 2,5 µg of a long-acting muscarinic antagonist (LAMA-tiotropium) administered via a spacer device” NCT05927155 ↗ “Spiriva Handihaler® contains Spiriva (also known as Tiotropium) and is administered via HandiHaler® device.” NCT03095456 ↗ “Inhaled Fenotereol,Ipratroium Plus Beclomethasone Versus Salmeterol,Tiotropium Plus Fluticasone” NCT05748977 ↗ “Taken as 1 capsule containing 18 µg of Tiotropium via the Handihaler DPI for 7 days” NCT01587079 ↗ “inhaled budesonide(160ug,bid),formotero(4.5ug,bid) and tiotropium bromide(18μg,qd)” NCT03504527 ↗ “Tiotropium is a once-daily, long-acting anticholinergic bronchodilator” PMID 25188297 ↗ Sep 2014 “Effect of Tiotropium (Spiriva) on Exercise Tolerance in COPD Patients” NCT00274508 ↗ “Spiriva (tiotropium) 18 mcg once daily (QD) via Handihaler” NCT02276222 ↗ “Spiriva® (tiotropium) 18 mcg, one inhalation once daily” NCT00496470 ↗ “18 μg Tiotropium [Spiriva® HandiHaler®]” NCT02254174 ↗ “Tiotropium 18 µg inhalation capsule” NCT02172807 ↗ “Tiotropium (Anticholinergic)” NCT06609941 ↗ “Tiotropium(inhaler)” NCT02790047 ↗ “Tiotropium” NCT04179461 ↗ “Tiotropium” NCT03662711 ↗ |
| Known as | Ba 79 BR | “The objective of this study is to investigate the long-term safety of Ba 79 BR (tiotropium) powder inhalation” NCT02172430 ↗ |
| Known as | Ba679BR | “A Multiple Dose Comparison of 18 µg, 36 µg of Ba679BR (Tiotropium) Inhalation Capsules and Oxitropium Metered Dose Inhaler (2 Puffs of 100µg) in a 4-week, Double-Blind,...” NCT02172807 ↗ |
| Known as | Bromuro de Tiotropio | “The objective of this study is to determine if tiotropium (Spiriva, Bromuro de Tiotropio) 18 mcg once daily by oral inhalation compared to placebo increases the magnitude of...” NCT00144326 ↗2“daily treatment with tiotropium (Spiriva®, Bromuro de Tiotropio®) inhalation capsule via HandiHaler® reduces the rate of decline in lung function over time in patients with COPD.” NCT00144339 ↗ “tiotropium inhalation capsules (Spiriva, Bromuro de Tiotropio)” NCT00157235 ↗ |
| Known as | GSP304 | “GSP304 (tiotropium bromide) Inhalation Solution” NCT03118765 ↗ |
| Known as | Neng Beile | “Tiotropium Bromide Spray (Si Lihua ® Neng Beile ®)” NCT05295355 ↗ |
| Known as | Si Lihua | “Tiotropium Bromide Spray (Si Lihua ® Neng Beile ®)” NCT05295355 ↗ |
| Known as | Spiriva | “The purpose of the study is to determine the efficacy and safety of the combination of ADVAIR DISKUS® 250/50mcg (FLUTICASONE PROPIONATE/SALMETEROL COMBINATION PRODUCT) plus...” NCT00784550 ↗42“The investigators will compare the reduction in Borg dyspnea score during the 3-min constant rate shuttle walking test after 3 weeks of indacaterol 110 µg/Glycopyrronium 50 µg...” NCT02567214 ↗ “The objective of this study is to determine if tiotropium (Spiriva, Bromuro de Tiotropio) 18 mcg once daily by oral inhalation compared to placebo increases the magnitude of...” NCT00144326 ↗ “The purpose of this study is to investigate the effect of a 9-month treatment of tiotropium (SPIRIVA®) 18 mcg once daily on Health Related Quality of Life and lung function in...” NCT00274053 ↗ “To evaluate acute effect of single dose of ipratropium (Atrovent) or fenoterol (Berotec) in comparison to placebo when given to COPD patients on pharmacodynamic steady state of...” NCT00274066 ↗ “Tiotropium Bromide Powder for Inhalation will be used to Group B and Group C patients: Tiotropium Bromide Powder for Inhalation(Spiriva®, Boehringer Ingelheim), 18μg/ capsule,...” NCT03745261 ↗ “daily treatment with tiotropium (Spiriva®, Bromuro de Tiotropio®) inhalation capsule via HandiHaler® reduces the rate of decline in lung function over time in patients with COPD.” NCT00144339 ↗ “tiotropium 18 μg, formulated as inhalation powder in the hard gelatine capsule and delivered via the HandiHaler® (Spiriva®) following single dose inhalation” NCT02242266 ↗ “Fixed Combination Of Fluticasone Furoate Plus Vilanterol Administered Via Dry Powder Inhaler (DPI) (Relvar®) Plus Tiotropium Bromide (Spiriva®)” NCT02467452 ↗ “Efficacy and Safety Comparison of Tiotropium Inhalation Solution (Respimat Inhaler) and Spiriva HandiHaler in COPD” NCT00239447 ↗ “a Free Combined Single Dose of 18 μg Tiotropium [Spiriva® HandiHaler®] and 50 μg Salmeterol [Serevent® Diskus®]” NCT02254174 ↗ “Spiriva Handihaler® contains Spiriva (also known as Tiotropium) and is administered via HandiHaler® device.” NCT03095456 ↗ “Tiotropium (Spiriva, Boehringer Ingelheim), a long-acting inhaled anticholinergic bronchodilator” NCT02683668 ↗ “Tiotropium (Spiriva®) is a once-daily inhaled anticholinergic for the treatment of COPD.” NCT00239421 ↗ “long acting bronchodilators "foradil/spiriva" or combined LABD and inhaled steroids” NCT02257463 ↗ “A Double-blind, Randomised Study to Assess the Influence of Tiotropium (Spiriva®)” NCT00257452 ↗ “tiotropium Handihaler® (Spiriva®) 18μg once daily for a duration of 4 weeks” NCT03964207 ↗ “Tiotropium Inhalation Solution (Respimat Inhaler) and Spiriva HandiHaler” NCT00281567 ↗ “Effect of Tiotropium (Spiriva) on Exercise Tolerance in COPD Patients” NCT00274508 ↗ “Tiotropium Bromide Inhalation Solution; Spiriva® Respimat® (Spiriva)” NCT02347072 ↗ “tiotropium inhalation capsule 18 ug (Spiriva inhalation capsule)” NCT00292448 ↗ “Tiotropium Inhalation Powder, hard gelatine capsule (Spiriva®)” NCT00668772 ↗ “tiotropium inhalation capsules (Spiriva, Bromuro de Tiotropio)” NCT00157235 ↗ “plus Spiriva HandiHaler (tiotropium 18 mcg) once daily” NCT03478683 ↗ “following treatment with tiotropium bromide (Spiriva)” NCT00274027 ↗ “Tiotropium (Spiriva) + Salbutamol (Ventolin)” NCT00981851 ↗ “Tiotropium (Spiriva) Rehabilitation Study” NCT00274521 ↗ “18 μg of tiotropium bromide \[Spiriva®\]” NCT01112241 ↗ “Spiriva capsules inhaled via HandiHaler” NCT04850144 ↗ “Spiriva HandiHaler (tiotropium 18 mcg)” NCT03478696 ↗ “tiotropium (Spiriva, 18 µg q.d.)” NCT00239499 ↗ “Tiotropium (Spiriva®)” NCT06679465 ↗ “Tiotropium (Spiriva®)” NCT00277264 ↗ “Tiotropium, Spiriva®” NCT00662740 ↗ “tiotropium (Spiriva)” NCT00144196 ↗ |
| Known as | Spiriva Handihaler | “a Free Combined Single Dose of 18 μg Tiotropium [Spiriva® HandiHaler®] and 50 μg Salmeterol [Serevent® Diskus®]” NCT02254174 ↗8“Inhaled tiotropium bromide 18 μg (Spiriva Handihaler®) administered QD for 7 days” NCT01085045 ↗ “open-label tiotropium bromide inhalation powder (Spiriva® Handihaler®)” NCT01854645 ↗ “Open-label tiotropium bromide inhalation powder (Spiriva® Handihaler®)” NCT01970878 ↗ “tiotropium (delivered by the Handihaler® as Spiriva Handihaler®)” NCT01696058 ↗ “Tiotropium (Spiriva® HandiHaler®, 18 µg Once Daily)” NCT01072396 ↗ “Open-label drug also known as Spiriva HandiHaler” NCT01124422 ↗ “18 mcg tiotropium (Spiriva HandiHaler) daily” NCT00525512 ↗ |
| Known as | Spiriva Respimat | “Tiotropium (Spiriva® Respimat®, Boehringer Ingelheim International) is approved as a once-daily maintenance treatment of asthma” NCT04990167 ↗4“tiotropium Respimat® (Spiriva® Respimat®) 5 microgram (μg) once daily for a duration of 4 weeks” NCT03964207 ↗ “Tiotropium Bromide Inhalation Solution; Spiriva® Respimat® (Spiriva)” NCT02347072 ↗ “tiotropium bromide monohydrate (Spiriva Respimat)” NCT04648813 ↗ |
| Known as | SpirivaTM | “Tiotropium (SpirivaTM) 18 μg/inhalation, 1 inhalation once daily” NCT01397890 ↗ |
| Known as | T18GEL | “18 µg Tiotropium (T18GEL) inhalation powder plus 50 µg Salmeterol MDPI (S\_DPI) twice daily (BID)” NCT00662792 ↗ |
| Known as | TIO | “The long-acting muscarinic antagonists umeclidinium (UMEC) and tiotropium (TIO) are approved once-daily maintenance therapies for COPD.” PMID 27103795 ↗ Apr 20165“with tiotropium bromide (TIO), 18 μg, on aPWV.” PMID 25058845 ↗ Dec 2014 “compared with tiotropium (TIO) 18 mcg/day” PMID 27796912 ↗ Oct 2016 “antimuscarinic tiotropium bromide (TIO)” PMID 20580216 ↗ Jun 2010 “once-daily tiotropium (TIO) 18 µg” PMID 25841237 ↗ Apr 2015 “Tiotropium 18 μg (TIO 18 μg)” NCT02796677 ↗ |
| Known as | Tio18GEL | “18 µg Tiotropium (Tio18GEL) inhalation powder” NCT00662792 ↗1“tiotropium (Tio18GEL)” NCT00668772 ↗ |
| Known as | Tiotropium Bromide | “A 12-week, Randomised, Placebo-controlled, Double-blind, Parallel Group, Multi-center Trial to Assess the Efficacy and Safety of Tiotropium Bromide (18 µg) Delivered Via the...” NCT01483625 ↗72“Dual Therapy (LABA + LAMA): Patients receive a long-acting beta-agonist (LABA) such as Formoterol, Salmeterol, Olodaterol, Vilanterol, or Indacaterol, in combination with a...” NCT07058259 ↗ “The objective of this trial is to evaluate whether the effect of one year (48 weeks) treatment with inhaled tiotropium bromide (Spiriva® - 18 µg once daily) on the change in...” NCT00277264 ↗ “The objectives of this study were to evaluate the effect of a one-year treatment with inhaled tiotropium bromide 18 mcg once daily on lung function, incidence and severity of...” NCT00274014 ↗ “A total of 839 patients with COPD who satisfied the eligibility criteria were randomly assigned (1:1) to receive a once daily inhaled capsule of either tiotropium bromide (18...” PMID 24549160 ↗ Feb 2014 “Open-label tiotropium bromide 18 μg capsules for inhalation once daily delivered via HandiHaler® device for at least 64 weeks of double blind treatment period (study duration...” NCT01120691 ↗ “Proof of Concept Evaluation of Drug-Device Interaction With Aclidinium Bromide Via Genuair® and Tiotropium Bromide Via HandiHaler® in COPD Using Impulse Oscillometry” NCT02039050 ↗ “Tiotropium bromide, long-acting muscarinic antagonist (LAMA). Administered as 2.5 μg per actuation, 2 inhalations once daily via Respimat inhaler for 28 days.” NCT07541378 ↗ “Fixed Combination Of Fluticasone Furoate Plus Vilanterol Administered Via Dry Powder Inhaler (DPI) (Relvar®) Plus Tiotropium Bromide (Spiriva®)” NCT02467452 ↗ “single inhaled doses of GSK573719 (250, 500 and 1000 μg) and Tiotropium Bromide (18 μg) Via DPI in COPD Patients.” NCT00515502 ↗ “1 time inhalation of 5 mcg of Tiotropium bromide by Respimat and 400 mcg of Salbutamol by Volume Spacer.” NCT00981851 ↗ “The objective of this study is to evaluate the effect of inhaled tiotropium bromide on trough FEV1” NCT00239460 ↗ “Orally Inhaled Tiotropium Bromide (2.5 and 5 µg Once Daily ) Delivered by the Respimat® Inhaler” NCT01257230 ↗ “Tiotropium Bromide Powder for Inhalation will be used once daily (18 μg each time) for 52 weeks” NCT04208581 ↗ “inhaled budesonide(160ug,bid),formotero(4.5ug,bid) and tiotropium bromide(18μg,qd)” NCT03504527 ↗ “Inhaled tiotropium bromide 18 μg (Spiriva Handihaler®) administered QD for 7 days” NCT01085045 ↗ “0.25 mg oral tablet plus tiotropium bromide 18 microgram once daily for 12 weeks” NCT01543919 ↗ “Tiotropium Bromide 18µg (Oral Inhalation, Delivered by the HandiHaler®)” NCT01040689 ↗ “Open-label tiotropium bromide inhalation powder (Spiriva® Handihaler®)” NCT01970878 ↗ “open-label tiotropium bromide inhalation powder (Spiriva® Handihaler®)” NCT01854645 ↗ “Tiotropium bromide (Spiriva) capsule 18μg once daily inhaled.” NCT03842839 ↗ “once-daily tiotropium bromide (18 μg) versus placebo” PMID 25289942 ↗ Nov 2014 “Tiotropium Bromide Spray (Si Lihua ® Neng Beile ®)” NCT05295355 ↗ “GSP304 (tiotropium bromide) Inhalation Solution” NCT03118765 ↗ “with tiotropium bromide (TIO), 18 μg, on aPWV.” PMID 25058845 ↗ Dec 2014 “Spiriva® Handihaler® (Tiotropium Bromide)” NCT01566773 ↗ “with tiotropium bromide 18 μg once daily” PMID 24124358 ↗ Oct 2013 “18 μg of tiotropium bromide \[Spiriva®\]” NCT01112241 ↗ “antimuscarinic tiotropium bromide (TIO)” PMID 20580216 ↗ Jun 2010 “tiotropium bromide 2.5µg once daily” NCT01233284 ↗ “inhaled tiotropium bromide” NCT02172378 ↗ “Drug: Tiotropium Bromide” NCT04990167 ↗ “Drug: Tiotropium bromide” NCT01437748 ↗ “Drug: Tiotropium Bromide” NCT04061161 ↗ “Drug: Tiotropium bromide” NCT00563381 ↗ “Drug: tiotropium bromide” NCT00412204 ↗ |
| Known as | Tiotropium Bromide Monohydrate | “Each actuation from the RESPIMAT inhaler delivers 3.124 mcg tiotropium bromide monohydrate (equivalent to 2.5 mcg tiotropium) and 2.736 mcg olodaterol hydrochloride (equivalent...” NCT02799784 ↗4“Micronized Tiotropium Bromide Monohydrate 22.5 mcg” NCT02441114 ↗ “tiotropium bromide monohydrate (Spiriva Respimat)” NCT04648813 ↗ |
| Known as | Tiotropium Bromide Powder for Inhalation (Spiriva) | “Tiotropium Bromide Powder for Inhalation (Spiriva®)” NCT03169504 ↗ |
| Known as | Tiotropium BromideInhalation Aerosol Suspension | “Tiotropium BromideInhalation Aerosol Suspension” NCT05295355 ↗ |
| Known as | Tiotropium Respimat | “Tiotropium Respimat® in asthma: a double-blind, randomised, dose-ranging study” PMID 24890738 ↗ Jun 2014 |
| Known as | tiotropium: Spiriva | “tiotropium: Spiriva” NCT00864812 ↗ |
| Known as | Trimbow | ClinicalTrials.gov intervention name — accepted as the source's own label NCT05495698 ↗ |
| Action | Inhibit | “the long-acting anticholinergic tiotropium” PMID 21807250 ↗ Aug 2011 |
| Modality | Other / unclassified | “once-daily long-acting anticholinergic” PMID 27812637 ↗ Sep 2016 |
| Route | Inhaled | “Tiotropium Bromide Inhalation Powder” NCT00106821 ↗ |