- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Platelet-derived growth factor.
Displaying page 1 of 1.
EudraCT Number: 2014-000973-38 | Sponsor Protocol Number: 14-026 | Start Date*: 2014-05-14 |
Sponsor Name:RWTH Aachen vertreten durch das CTC-A | ||
Full Title: Xenon-inhalation: elimination of xenon and its effect on erythropoetin-levels in blood of healthy volunteers | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-001056-19 | Sponsor Protocol Number: HUPA-EC-02-2012 | Start Date*: 2013-12-01 | |||||||||||
Sponsor Name:FUNDACIÓN PARA LA INVESTIGACIÓN BIOMÉDICA DEL HOSPITAL UNIVERSITARIO PRÍNCIPE DE ASTURIAS | |||||||||||||
Full Title: ROLE OF BIOLOGICAL THERAPY IN ROTATOR CUFF TENDINOPATHY. EFFECTIVENESS OF PLASMA RICH IN GROWTH FACTOR (PRGF-ENDORET)REGARDING TO FUNCTIONAL CAPACITY AND PAIN COMPARED WITH THE CONVENTIONAL TREATME... | |||||||||||||
Medical condition: ROTATOR CUFF TENDINOPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016914-25 | Sponsor Protocol Number: CEDRICStudie | Start Date*: 2011-08-08 |
Sponsor Name:Deutsches Herzzentrum Berlin | ||
Full Title: CEDRIC: Clopidogrel- Effects on Diameter Reduction and Intimal Hyperplasia in Long-term Follow up after Cardiac Transplantation | ||
Medical condition: Transplant vasculopathy after heart transplantation characterized by Stanford type B2 lesions in coronary angiography and by microvasculopathy proven in biopsy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006728-73 | Sponsor Protocol Number: GENOM-008 | Start Date*: 2009-03-09 |
Sponsor Name:GRUPO ESPAÑOL DE NEUROONCOLOGIA MEDICA | ||
Full Title: Ensayo Clínico abierto, fase II, de tratamiento neo-adyuvante de Sunitinib (SU11248) previo al tratamiento con irradiación y concomitante a la misma, en pacientes con Glioblastoma RPA-V-VI y sólo b... | ||
Medical condition: Glioblastoma clase RPA V-VI, no resecable | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001724-35 | Sponsor Protocol Number: AMASCIS-02 | Start Date*: 2020-06-16 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario de La Paz (FIBHULP) | |||||||||||||
Full Title: AMASCIS-02. ALOGENIC ADIPOSE TISSUE-DERIVED MESENCHYMAL STEM CELLS IN ISCHEMIC STROKE. A PHASE IIB MULTICENTER DOUBLE BLIND PLACEBO CONTROLLED CLINICAL TRIAL. | |||||||||||||
Medical condition: Moderate-severe ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000922-12 | Sponsor Protocol Number: TV44400-CNS-40083 | Start Date*: 2016-01-04 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries, Ltd | |||||||||||||
Full Title: A Multinational, Multicenter, Randomized, Parallel Group, Open-Label Study to Assess Medication Satisfaction in Patients with Relapsing Remitting Multiple Sclerosis (RRMS) Treated with Subcutaneous... | |||||||||||||
Medical condition: Relapsing-Remitting Multiple Sclerosis (RRMS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) DE (Completed) IE (Completed) PL (Completed) FI (Completed) ES (Completed) HR (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001747-31 | Sponsor Protocol Number: P160907 | Start Date*: 2019-04-09 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: A Multi-center, Randomised, Double-blind Trial of Nintedanib in Lung Tranplant (LTx) recipients with bronchiolitis obliterans sydrome (BOS) grade 1-2 | |||||||||||||
Medical condition: Bronchiolitis Obliterating Syndrome (SBO) grade 1 or 2 in patients with pulmonary transplantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001157-48 | Sponsor Protocol Number: 20HH5896 | Start Date*: 2020-07-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||||||||||||||||||||||
Full Title: Identifying a safe and tolerated dose of Imatinib for patients with Pulmonary Arterial Hypertension (PAH) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Pulmonary Arterial Hypertension (Idiopathic, heritable, or assosicated with anorexigens) | ||||||||||||||||||||||||||||||||||||||
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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: 2009-017147-33 | Sponsor Protocol Number: AGMT_CMML1 | Start Date*: 2010-02-10 | |||||||||||
Sponsor Name:AGMT gemeinnützige GmbH | |||||||||||||
Full Title: A Phase I/II Study of Lenalidomide in Patients with Chronic Myelomonocytic Leukemia | |||||||||||||
Medical condition: Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009035-30 | Sponsor Protocol Number: CP15-0802 | Start Date*: 2009-10-27 | |||||||||||
Sponsor Name:ImClone LLC | |||||||||||||
Full Title: Randomized Phase 2 Trial Investigating Liposomal Doxorubicin With or Without Anti Platelet Derived Growth Factor Receptor-Alpha (PDGFRα) Monoclonal Antibody IMC-3G3 in Patients With Platinum-Refrac... | |||||||||||||
Medical condition: Platinium-refractory or Platinium-resistant Advanced Ovarian Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001282-40 | Sponsor Protocol Number: MORAb-004-201-Mel | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Morphotek Inc | |||||||||||||
Full Title: A Study of the Efficacy and PK/PD Relationship of Monotherapy MORAb-004 in Subjects with Metastatic Melanoma | |||||||||||||
Medical condition: Metastaic Melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004370-10 | Sponsor Protocol Number: RUXO_LMMC-PRO_1401 | Start Date*: 2014-03-21 | |||||||||||
Sponsor Name:Grupo Español de Sindromes Mielodisplásicos (GESMD) | |||||||||||||
Full Title: A phase II study of ruxolitinib (INCB018424) to evaluate efficacy and safety in Patients with Proliferative Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
Medical condition: Proliferative Chronic Myelomonocytic Leukemia (CMML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023854-35 | Sponsor Protocol Number: CD-ON-MEDI-575-1031 | Start Date*: 2011-11-07 | ||||||||||||||||
Sponsor Name:MedImmune, LLC | ||||||||||||||||||
Full Title: A Phase 1b/2 Randomized Study of MEDI-575 in Combination With Carboplatin Plus Paclitaxel Versus Carboplatin Plus Paclitaxel Alone in Adult Subjects With Previously Untreated, Advanced Non-Small Ce... | ||||||||||||||||||
Medical condition: Previously untreated advanced non-small cell lung cancer in adults | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) HU (Completed) BG (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003874-29 | Sponsor Protocol Number: E-3810-II-02 | Start Date*: 2014-01-20 | |||||||||||
Sponsor Name:EOS S.p.A. | |||||||||||||
Full Title: A single arm, open-label, phase II study to assess the efficacy of the dual VEGFR-FGFR tyrosine kinase inhibitor, lucitanib, given orally as a single agent to patients with FGFR1-driven lung cancer | |||||||||||||
Medical condition: FGFR1-amplified squamous non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
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