- Trials with a EudraCT protocol (2,324)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,324 result(s) found for: Pulmonary Disease.
Displaying page 62 of 117.
EudraCT Number: 2012-003990-24 | Sponsor Protocol Number: VX12-809-104 | Start Date*: 2013-06-25 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 3, Randomized, Double Blind, Placebo Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Lumacaftor in Combination With Ivacaftor in Subjects Aged 12 Years and Older Wit... | |||||||||||||
Medical condition: Cystic fibrosis in patients homozygous for the F508del-CFTR Mutation | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) AT (Completed) GB (Completed) ES (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003531-21 | Sponsor Protocol Number: Debio 0614-202 | Start Date*: 2009-05-05 | |||||||||||
Sponsor Name:DEBIOPHARM S.A. | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled parallel-group phase IIb study of the safety and efficacy of istaroxime over 24 hours at three doses in acute decompensated heart failure... | |||||||||||||
Medical condition: acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) LT (Prematurely Ended) PL (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005059-35 | Sponsor Protocol Number: TMP-2204-2021-47 | Start Date*: 2022-01-25 | ||||||||||||||||
Sponsor Name:F4-Pharma GmbH i.G. | ||||||||||||||||||
Full Title: Potential of FX06 to improve disease severity in Acute Respiratory Distress Syndrome patients (Ixion 2.0) | ||||||||||||||||||
Medical condition: Acute Respiratory Distress Syndrome (ARDS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) LT (Trial now transitioned) PT (Prematurely Ended) IT (Prematurely Ended) NL (Completed) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003685-32 | Sponsor Protocol Number: PB-06-007 | Start Date*: 2012-01-27 | |||||||||||
Sponsor Name:Protalix Biotherapeutics | |||||||||||||
Full Title: A Multicenter Extension Study of Taliglucerase alfa in Adult Subjects with Gaucher Disease | |||||||||||||
Medical condition: Gaucher disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004800-23 | Sponsor Protocol Number: RG-17-241 | Start Date*: 2018-06-12 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: A comparison of reduced dose total body irradiation (TBI) and cyclophosphamide with fludarabine and melphalan reduced intensity conditioning in adults with acute lymphoblastic leukaemia (ALL) in co... | |||||||||||||
Medical condition: Acute Lymphoblastic Leukaemia (ALL) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000046-21 | Sponsor Protocol Number: C0524T03 | Start Date*: 2004-11-22 |
Sponsor Name:Centocor BV | ||
Full Title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Dose-ranging Study Evaluating the Efficacy and Safety of CNTO 148 Administered Subcutaneously in Symptomatic Su... | ||
Medical condition: Severe persistent asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) CZ (Prematurely Ended) SE (Prematurely Ended) GB (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-005624-26 | Sponsor Protocol Number: 03-CL-1401 | Start Date*: 2016-05-30 | |||||||||||||||||||||
Sponsor Name:Windtree Therapeutics, Inc. (formerly Discovery Laboratories, Inc.) | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Open-Label, Controlled Trial to Assess the Safety and Tolerability of Lucinactant for Inhalation in Preterm Neonates 26 to 28 Weeks PMA. | |||||||||||||||||||||||
Medical condition: Respiratory Distress Syndrome (RDS) | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001743-12 | Sponsor Protocol Number: INCB24360-208 | Start Date*: 2018-07-04 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2, Open-Label, Dose-Escalation, Safety, Tolerability, and Efficacy Study of Epacadostat and Nivolumab in Combination With Immune Therapies in Subjects With Advanced or Metastatic Maligna... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Phase 1 (Dose Escalation): Advanced or metastatic solid tumors. Phase 2 (Dose Expansion): Advanced or metastatic non–small cell lung cancer (NSCLC), unresectable or metastatic melanoma (MEL) and r... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023090-19 | Sponsor Protocol Number: SMR 2375 | Start Date*: 2011-03-29 | |||||||||||
Sponsor Name:AlgiPharma AS | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, cross-over study to evaluate the safety, tolerability and preliminary efficacy of alginate oligosaccharide (OligoG) administered for 28 days in subje... | |||||||||||||
Medical condition: Cystic Fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004355-40 | Sponsor Protocol Number: rhLAMAN-04 | Start Date*: 2012-01-17 |
Sponsor Name:Zymenex A/S | ||
Full Title: A multi-center, open-label trial of the long-term efficacy and safety of Lamazym for the treatment of patients with alpha-Mannosidosis. | ||
Medical condition: Treatement of Alpha-Mannosidosis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011289-27 | Sponsor Protocol Number: CF001 | Start Date*: 2009-04-22 | |||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
Full Title: Probiotics in Cystic Fibrosis | |||||||||||||
Medical condition: Cystic Fibrosis Patients | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001393-16 | Sponsor Protocol Number: SHP607-202 | Start Date*: 2019-06-21 | |||||||||||
Sponsor Name:Premacure AB | |||||||||||||
Full Title: A Phase 2b, Multicenter, Randomized, Open-label, Controlled, 3-Arm Study to Evaluate the Clinical Efficacy and Safety of SHP607 in Preventing Chronic Lung Disease Through 12 Months Corrected Age Co... | |||||||||||||
Medical condition: Chronic Lung Disease | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Trial now transitioned) SE (Prematurely Ended) FR (Completed) DE (Trial now transitioned) PT (Trial now transitioned) ES (Temporarily Halted) FI (Trial now transitioned) NL (Trial now transitioned) PL (Prematurely Ended) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001977-82 | Sponsor Protocol Number: RA4104917 | Start Date*: 2005-09-09 |
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
Full Title: A randomised, double-blind, placebo-controlled, parallel group study to investigate the safety, tolerability, pharmacokinetics and effect on synovial thickness and vascularity of 28 days repeat dos... | ||
Medical condition: Rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-008209-22 | Sponsor Protocol Number: AMC002 | Start Date*: 2009-02-25 |
Sponsor Name:Academic Medical Center | ||
Full Title: Chemoradiation combined with panitumumab followed by surgery for patients with operable esophageal cancer | ||
Medical condition: Surgical resectable: T2-3, N0-1, M0 adenocarcinomas, undifferentiated or squamous cell carcinomas of the esophagus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001413-42 | Sponsor Protocol Number: MPD-RC 101 | Start Date*: 2007-06-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Study of Fludarabine based conditioning for Allogeneic Stem cell Transplantation for Myelofibrosis | |||||||||||||
Medical condition: MYELOFIBROSIS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000978-68 | Sponsor Protocol Number: | Start Date*: 2006-12-18 |
Sponsor Name:AstraZeneca | ||
Full Title: Treatment of systemic effects in patients with COPD | ||
Medical condition: Chronic obstructive pulmonary disease (COPD) is a preventable and treatable disease state characterized by airflow limitation that is not fully reverible. The airflow limitation is usually progress... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004864-24 | Sponsor Protocol Number: COPD-1 | Start Date*: 2013-07-09 |
Sponsor Name:Bionorica SE | ||
Full Title: Randomized, placebo-controlled, double-blind, cross-over trial with Bronchipret and Sinupret to evaluate acceleration of mucociliary clearance (MCC) | ||
Medical condition: PR1: Acceleration of mucociliary clearance as a therapeutic effect when treating inflammation of the nasal sinuses PR2: Acceleration of mucociliary clearance as a therapeutic effect when treating ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001696-16 | Sponsor Protocol Number: SOLUCOM | Start Date*: 2021-10-28 | ||||||||||||||||||||||||||
Sponsor Name:Vestre Viken Health Trust | ||||||||||||||||||||||||||||
Full Title: Sotorasib in advanced KRASG12C-mutated non-small cell lung cancer patients with comorbidities | ||||||||||||||||||||||||||||
Medical condition: Advanced KRASG12C-mutated non-small cell lung cancer patients with comorbidities | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NO (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023777-19 | Sponsor Protocol Number: SToP-BPD | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Systemic Hydrocortisone To Prevent Bronchopulmonary Dysplasia in preterm infants: the SToP-BPD study | |||||||||||||
Medical condition: bronchopulmonary dysplasia | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000381-29 | Sponsor Protocol Number: SCY-078-301 | Start Date*: 2017-07-17 |
Sponsor Name:SCYNEXIS, Inc. | ||
Full Title: Open-Label Study to Evaluate the Efficacy and Safety of Ibrexafungerp in Patients with Fungal Diseases that are Refractory to, Resistant to or Intolerant of Standard Antifungal Treatment (FURI) | ||
Medical condition: Patients > 18 years of age with a documented invasive and/or severe fungal disease that has been intolerant, resistant or refractory (rIFI) to Standard of Care (SoC) antifungal treatment. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
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