- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
21 result(s) found for: Transforming growth factor beta.
Displaying page 1 of 2.
| EudraCT Number: 2005-005482-10 | Sponsor Protocol Number: RN1001-0042 | Start Date*: 2006-03-13 |
| Sponsor Name:Renovo | ||
| Full Title: A double blind, placebo controlled, randomised dose response trial to investigate the efficacy of Juvista in the improvement of scar appearance when applied to approximated wound margins following ... | ||
| Medical condition: Patients undergoing varicose vein removal with ligation and stripping. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) LT (Completed) LV (Completed) BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-004938-24 | Sponsor Protocol Number: RN1001-0098 | Start Date*: 2009-03-24 | |||||||||||
| Sponsor Name:Renovo | |||||||||||||
| Full Title: A within patient, placebo controlled, proof of concept trial to assess the efficacy of Juvista in improving the appearance of existing scars that are 2-6 months old. | |||||||||||||
| Medical condition: Improvement of existing scars | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-004265-42 | Sponsor Protocol Number: RN1001-0041 | Start Date*: 2006-04-06 |
| Sponsor Name:Renovo | ||
| Full Title: A double blind, placebo controlled, randomised trial to investigate the efficacy of Juvista in the improvement of scar appearance in patients undergoing bilateral reduction mammaplasty. | ||
| Medical condition: Severe scarring following breast reduction surgery. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000994-30 | Sponsor Protocol Number: VD1.3 | Start Date*: 2013-02-19 |
| Sponsor Name:Medizinische Universität Graz | ||
| Full Title: A randomized, double‐blind, placebo controlled trial to evaluate the effects of vitamin D supplementation on metabolic and fertility parameters in PCOS women | ||
| Medical condition: Polycystic Ovary Syndrome | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-002124-28 | Sponsor Protocol Number: RN1001-0091 | Start Date*: 2008-11-17 | |||||||||||
| Sponsor Name:Renovo Ltd | |||||||||||||
| Full Title: A double blind, within patient, placebo controlled trial to assess the efficacy of Juvista (avotermin) in conjunction with scar revision surgery for the improvement of disfiguring scars. | |||||||||||||
| Medical condition: Improvement of scar appearance | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) FR (Completed) HU (Completed) ES (Completed) DK (Completed) IT (Completed) DE (Completed) LV (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006637-19 | Sponsor Protocol Number: CARDIOL100-002 | Start Date*: 2022-12-01 | |||||||||||
| Sponsor Name:Cardiol Therapeutics Inc. | |||||||||||||
| Full Title: Impact of CardiolRxTM on Myocardial Recovery in Patients with Acute Myocarditis A double-blind, placebo-controlled trial (ARCHER) | |||||||||||||
| Medical condition: Acute Myocarditis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003575-11 | Sponsor Protocol Number: VitaminD&TT | Start Date*: 2013-03-05 | |||||||||||
| Sponsor Name:Medizinische Universität Graz, Innere Medizin | |||||||||||||
| Full Title: A randomized, double-blind, placebo controlled trial to evaluate the effects of vitamin D supplementation on androgen levels in hypogonadal men | |||||||||||||
| Medical condition: Male hypogonadism (total testosterone <3ng/ml) | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003818-24 | Sponsor Protocol Number: DC2015RED01 | Start Date*: 2015-12-11 |
| Sponsor Name:VU University Medical Center | ||
| Full Title: A phase 4, monocenter, randomized, double-blind, comparator-controlled, parallel-group, mechanistic intervention trial to assess the effect of 12-week treatment with the sodium-glucose linked trans... | ||
| Medical condition: Type 2 Diabetes Mellitus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001280-13 | Sponsor Protocol Number: A536-05 | Start Date*: 2014-09-03 | ||||||||||||||||
| Sponsor Name:Acceleron Pharma Inc. | ||||||||||||||||||
| Full Title: An Open-Label Extension Study to Evaluate the Long-Term Effects of ACE-536 for the Treatment of Anemia in Patients with Low or Intermediate-1 Risk Myelodysplastic Syndromes (MDS) Previously Enrolle... | ||||||||||||||||||
| Medical condition: Myelodysplastic Syndromes (MDS) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-001547-12 | Sponsor Protocol Number: DC2017RACELINES01 | Start Date*: 2017-12-21 |
| Sponsor Name:VU University Medical Center | ||
| Full Title: A phase 4, monocenter, randomized, double-blind, comparator-controlled, 3-armed parallel mechanistic intervention trial to assess the effect of 8-week empagliflozin (SGLT-2 inhibitor) monotherapy, ... | ||
| Medical condition: Type 2 Diabetes Mellitus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003301-26 | Sponsor Protocol Number: IAFIPF001 | Start Date*: 2013-09-20 | |||||||||||
| Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: A randomised placebo-controlled pilot trial of omeprazole in idiopathic pulmonary fibrosis (IPF) | |||||||||||||
| Medical condition: Idiopathic Pulmonary Fibrosis (IPF) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002093-20 | Sponsor Protocol Number: H9H-MC-JBEF | Start Date*: 2017-03-16 |
| Sponsor Name:Eli Lilly and Company | ||
| Full Title: A Phase 1b/2 Dose Escalation and Cohort Expansion Study of the Safety, Tolerability and Efficacy of a Novel Transforming Growth Factor-beta Receptor I Kinase Inhibitor (Galunisertib) Administered i... | ||
| Medical condition: Advanced Refractory Solid Tumours (Phase 1b) and in Recurrent or Refractory Non–Small Cell Lung Cancer or Hepatocellular Carcinoma, (Phase 2) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001626-26 | Sponsor Protocol Number: OMT28-C0201 | Start Date*: 2019-01-23 | |||||||||||
| Sponsor Name:OMEICOS Therapeutics GmbH | |||||||||||||
| Full Title: A Placebo-controlled, double-blind, Randomized, dose finding phase II study on OMT-28 in MaIntenance of Sinus rhythm after Electrical cardioversion in patients with persistent Atrial Fibrillation (... | |||||||||||||
| Medical condition: Persistent atrial fibrillation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) BG (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002530-50 | Sponsor Protocol Number: EspeRare_RIM_001 | Start Date*: 2015-11-04 | |||||||||||
| Sponsor Name:EspeRare | |||||||||||||
| Full Title: A phase Ib, open label study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending oral doses of Rimeporide in patients with Duchenne Muscular Dystrophy. | |||||||||||||
| Medical condition: Duchenne Muscular Dystrophy (DMD) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: ES (Completed) GB (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-005096-27 | Sponsor Protocol Number: MBPS205 | Start Date*: 2017-06-23 | |||||||||||
| Sponsor Name:Mereo BioPharma 3 Ltd. | |||||||||||||
| Full Title: A Phase 2b, Multicentre, Multinational, Double-blind, Dose-finding Study, incorporating an open label substudy, in Adult Patients with Type I, III or IV Osteogenesis Imperfecta Treated with setrusu... | |||||||||||||
| Medical condition: Osteogenesis imperfecta | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005036-26 | Sponsor Protocol Number: FXT-05 | Start Date*: 2011-11-29 | ||||||||||||||||||||||||||
| Sponsor Name:Funxional Therapeutics Ltd | ||||||||||||||||||||||||||||
| Full Title: An Exploratory Phase IIa Study to Investigate the Biological Activity of Oral FX125L in Adult Patients with Chronic Inflammatory Disease | ||||||||||||||||||||||||||||
| Medical condition: Asthma Chronic obstructive pulmonary disease Rheumatoid arthritis Psoriasis | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-001641-24 | Sponsor Protocol Number: PYR-311 | Start Date*: 2014-09-29 | |||||||||||
| Sponsor Name:NephroGenex | |||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the Safety and Efficacy of Pyridorin® (pyridoxamine dihydrochloride) in Subjects With Nephropathy Due to Type ... | |||||||||||||
| Medical condition: Nephropathy Due to Type 2 Diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004941-34 | Sponsor Protocol Number: GFT505B-319-1 | Start Date*: 2020-10-09 | |||||||||||
| Sponsor Name:IPSEN Pharma SAS | |||||||||||||
| Full Title: A Double-blind Randomized, Placebo-Controlled Study and Open-label Long Term Extension to Evaluate the Efficacy and Safety of Elafibranor 80 mg in Patients with Primary Biliary Cholangitis with Ina... | |||||||||||||
| Medical condition: Primary Biliary Cholangitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021994-35 | Sponsor Protocol Number: A4001098 | Start Date*: 2011-06-30 | |||||||||||
| Sponsor Name:ViiV Healthcare UK Limited | |||||||||||||
| Full Title: A Multicenter, Randomized, Blinded, Placebo Controlled Study To Evaluate The Safety Of Maraviroc In Combination With Other Antiretroviral Agents In HIV-1 Infected Subjects Coinfected With Hepatitis... | |||||||||||||
| Medical condition: HIV infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) DE (Completed) GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005983-12 | Sponsor Protocol Number: INT01/12 | Start Date*: 2012-03-21 | ||||||||||||||||||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||||||||||||
| Full Title: Phase II study of the fully human monoclonal antibody against transforming growth factor-beta (TGF-beta) receptor ALK1 (PF-03446962) in relapsed or refractory urothelial cancer (UC) failing first-l... | ||||||||||||||||||||||||||||
| Medical condition: Relapsed or refractory urothelial cancer after failure of 1st line platinum-containing chemotherapy regimen for metastatic disease. | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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