- Trials with a EudraCT protocol (564)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
564 result(s) found for: Pulmonary infection.
Displaying page 1 of 29.
| EudraCT Number: 2007-005045-38 | Sponsor Protocol Number: Colistina | Start Date*: 2007-10-02 | |||||||||||
| Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
| Full Title: Pharmacokinetic and colimicine (ColistinaR) concentrations in broncho alveolar lavage in patients affected by pulmonary infections caused by Gram - bacteria. | |||||||||||||
| Medical condition: pulmonary disease caused by Gram - infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-003725-22 | Sponsor Protocol Number: KKS-306 | Start Date*: 2023-04-20 | |||||||||||||||||||||
| Sponsor Name:Justus-Liebig-University Gießen | |||||||||||||||||||||||
| Full Title: Acute effect of iloprost (Ventavis®) inhalation in patients with exercise-induced pulmonary hypertension after a COVID-19 infection | |||||||||||||||||||||||
| Medical condition: Exercise-induced pulmonary hypertension after a COVID-19 infection | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-001929-40 | Sponsor Protocol Number: AZT_DSTB_BB | Start Date*: 2017-11-21 | |||||||||||
| Sponsor Name:University Medical Center Groningen | |||||||||||||
| Full Title: A prospective, randomized pilot study of the immunomodulatory effects of azithromycin in adults with pulmonary tuberculosis | |||||||||||||
| Medical condition: Pulmonary tuberculosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-003562-42 | Sponsor Protocol Number: AdjuVIT v3 | Start Date*: 2006-09-27 | |||||||||||
| Sponsor Name:Queen Mary, University of London | |||||||||||||
| Full Title: Trial of Adjunctive Vitamin D in Tuberculosis Treatment (AdjuVIT) | |||||||||||||
| Medical condition: Pulmonary tuberculosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001623-13 | Sponsor Protocol Number: T3inj-02/Thy-Support | Start Date*: 2020-05-20 | |||||||||||
| Sponsor Name:Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A. | |||||||||||||
| Full Title: Triiodothyronine for the treatment of critically ill patients with COVID-19 infection (Thy-Support Study) | |||||||||||||
| Medical condition: ICU patients diagnosed with pulmonary infection due to COVID-19 and require mechanical respiratory support or ECMO | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002514-40 | Sponsor Protocol Number: CISTA-TB | Start Date*: 2019-10-31 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
| Full Title: Phase II study on the safety and efficacy of cysteamine in association with standard tuberculosis therapy for the treatment of patients with pulmonary tuberculosis: a new therapy for tuberculosis d... | |||||||||||||
| Medical condition: Pulmonary Mycobacterium tuberculosis infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001585-14 | Sponsor Protocol Number: EPJ-2012 | Start Date*: 2013-01-10 | ||||||||||||||||
| Sponsor Name:FISEVI | ||||||||||||||||||
| Full Title: Effect of the elimination of colonization by Pneumocystis jirovecii on inflammatory response in patients with chronic obstructive pulmonary disease | ||||||||||||||||||
| Medical condition: Chronic obstructive pulmonary disease | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-002982-33 | Sponsor Protocol Number: 2020-PDNO-002 | Start Date*: 2021-03-02 | |||||||||||
| Sponsor Name:Attgeno AB | |||||||||||||
| Full Title: An open-label, multicenter study to evaluate the efficacy, safety and tolerability of PDNO (nitrosooxypropanol) infusion in COVID-19 patients with acute pulmonary hypertension | |||||||||||||
| Medical condition: Acute pulmonary hypertension during COVID-19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004554-32 | Sponsor Protocol Number: PC_ASP_006 | Start Date*: 2022-07-09 | |||||||||||
| Sponsor Name:Pulmocide Ltd | |||||||||||||
| Full Title: A double-blind, randomized, placebo-controlled study to assess the safety and efficacy of nebulized PC945 when added to systemic antifungal therapy for the treatment of refractory invasive pulmonar... | |||||||||||||
| Medical condition: Refractory invasive pulmonary aspergillosis (IPA) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) AT (Trial now transitioned) GR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004971-42 | Sponsor Protocol Number: RVT-1201-2002 | Start Date*: 2021-10-26 | |||||||||||
| Sponsor Name:Altavant Sciences GmbH | |||||||||||||
| Full Title: A Phase 2b, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Rodatristat Ethyl in Patients with Pulmonary Arterial Hypertension | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) FR (Completed) BE (Completed) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) ES (Ongoing) AT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002518-42 | Sponsor Protocol Number: FIBRO-COVID | Start Date*: 2020-07-20 | ||||||||||||||||
| Sponsor Name:IDIBELL | ||||||||||||||||||
| Full Title: A RANDOMIZED PHASE-II CLINICAL TRIAL TO EVALUATE THE EFFECT OF PIRFENIDONE COMPARED WITH PLACEBO IN PULMONARY FIBROSIS POST-COVID 19: | ||||||||||||||||||
| Medical condition: Pulmonary fibrosis induced by SARS-COV2 virus (post-COVID19 pulmonary sequelae) | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-003810-35 | Sponsor Protocol Number: BMX-04-001 | Start Date*: 2023-04-25 | ||||||||||||||||
| Sponsor Name:BiomX Ltd. | ||||||||||||||||||
| Full Title: A Phase 1b/2a, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate Nebulized Bacteriophage Treatment in Outpatient Adult Cystic Fibrosis (CF) Subjects with Chronic Pseudomon... | ||||||||||||||||||
| Medical condition: Cystic fibrosis Chronic Pseudomonas Aeruginosa Infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) NL (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-004295-18 | Sponsor Protocol Number: DRTB-HDT | Start Date*: 2022-11-21 | |||||||||||
| Sponsor Name:The Aurum Institute | |||||||||||||
| Full Title: A randomized controlled trial of two adjunctive host-directed therapies in rifampin-resistant tuberculosis (DRTB-HDT) | |||||||||||||
| Medical condition: Rifampin-resistant pulmonary tuberculosis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-000224-41 | Sponsor Protocol Number: IDANAT2 | Start Date*: 2008-08-26 | |||||||||||
| Sponsor Name:University of Cologne | |||||||||||||
| Full Title: A double-blind, multicentre, parallel group, randomised, controlled trial to evaluate the possible benefit of isoniazid dose adjustment according to the genotype for NAT2 (arylamine N-acetyltransfe... | |||||||||||||
| Medical condition: pulmonary tuberculosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005229-31 | Sponsor Protocol Number: 242-07-204 | Start Date*: 2008-02-14 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development and Commercialization, Inc. | |||||||||||||
| Full Title: A Multi center, Randomized, Double-blind, Placebo-controlled Phase 2 Trial to Evaluate the Safety, Efficacy and Pharmacokinetics of Multiple Doses of OPC-67683 in Patients with Pulmonary Sputum Cu... | |||||||||||||
| Medical condition: Pulmonary Multidrug-resistant Tuberculosis (MDR TB) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002202-30 | Sponsor Protocol Number: R207910BAC2001 | Start Date*: 2004-10-18 |
| Sponsor Name:Tibotec Pharmaceuticals Ltd. | ||
| Full Title: An open label study to evaluate the effects on Mycobacterium tuberculosis, safety, tolerability and pharmacokinetics of single doses of R207910, in treatment naive patients with mycobacterium tuber... | ||
| Medical condition: Tuberculosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-001564-31 | Sponsor Protocol Number: AMB 222 | Start Date*: 2005-10-07 | |||||||||||
| Sponsor Name:Myogen Inc. | |||||||||||||
| Full Title: A phase 2, Open-label, Multicenter Study Evaluating Ambrisentan in Subjects with Pulmonary Arterial Hypertension Who Have Previously Discontinued Endothelin Receptor Antagonist Therapy Due to Serum... | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022271-59 | Sponsor Protocol Number: 242-09-213 | Start Date*: 2011-07-19 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group Trial to Evaluate the Safety and Efficacy of Delamanid (OPC-67683) Administered Orally as 200 mg Total Daily Dos... | |||||||||||||
| Medical condition: Pulmonary Multidrug-resistant Tuberculosis (MDR TB) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) EE (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003633-24 | Sponsor Protocol Number: UITB-Study-29 | Start Date*: 2009-01-08 | |||||||||||
| Sponsor Name:TB Investigation Unit of Barcelona | |||||||||||||
| Full Title: Evaluation of a rifapentine-containing regimen for intensive phase treatment of pulmonary tuberculosis Evaluación de una Pauta con Rifapentina para la Fase Intensiva del tratamiento de la Tub... | |||||||||||||
| Medical condition: To compare two treatments for Pulmonary Tuberculosis Comparar dos tratamientos para la tuberculosis pulmonar | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014944-13 | Sponsor Protocol Number: 242-08-210 | Start Date*: 2009-11-06 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 2, Multi-center, Non-controlled, Open-label Dose Escalation Trial to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Orally Administered OPC-67683 Two Times Daily to Pati... | |||||||||||||
| Medical condition: Pulmonary Multidrug-resistant Tuberculosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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