- Trials with a EudraCT protocol (231)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
231 result(s) found for: Cell replacement therapy.
Displaying page 1 of 12.
EudraCT Number: 2008-003654-15 | Sponsor Protocol Number: 080314 | Start Date*: 2008-09-22 | |||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||
Full Title: Oral 1 mg oestradiol (E2) / 2 mg of drosperinone (DRSP) and 1 mg of oestradiol / 0.5 mg of norethisteroneacetate (NETA): effects on mammografic density and breast epithelial proliferation - an expl... | |||||||||||||
Medical condition: The effect of hormonal treatment on mammographic density and breast epithelial proliferation in postmenopausal women. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005491-20 | Sponsor Protocol Number: 20151205 | Start Date*: 2016-08-29 |
Sponsor Name:Actavis Hungary Gyógyszermarketing és Kereskedelmi Korlátolt Felelősségű Társaság | ||
Full Title: The effect of pancreatic enzyme replacement therapy on glucose metabolism, nutritional parameters, incretin response and beta-cell function in patients with diabetes mellitus and exocrine pancreati... | ||
Medical condition: To study the patients with diabetes mellitus (type 1, 2 and 3c) and exocrine pancreatic insufficiency. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003184-65 | Sponsor Protocol Number: TPL107 | Start Date*: 2020-02-24 |
Sponsor Name:Vifor Pharma | ||
Full Title: POREIIL - Postoperative replacement of intraoperative iron losses | ||
Medical condition: perioperative bleeding induced iron losses and anemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000746-22 | Sponsor Protocol Number: 874-2017 | Start Date*: 2017-06-22 |
Sponsor Name:Department of Dermatology, Zealand University Hospital, Roskilde | ||
Full Title: Vascular changes in basal cell carcinoma undergoing either electrochemotherapy or photodynamic therapy - assessed with optical coherence tomography | ||
Medical condition: Basal cell carcinoma in adults | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022072-31 | Sponsor Protocol Number: R5242A789 | Start Date*: 2013-04-15 | |||||||||||
Sponsor Name:RJAH Orthopaedic Hospital | |||||||||||||
Full Title: Autologous Cell Therapy for Osteoarthritis: An evaluation of the safety and efficacy of autologous transplantation of articular chondrocytes and/or bone marrow-derived stromal cells to repair chond... | |||||||||||||
Medical condition: osteochondral defects of the knee (early osteoarthritis) | |||||||||||||
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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: 2015-001452-30 | Sponsor Protocol Number: 010815testis | Start Date*: 2015-12-07 | |||||||||||
Sponsor Name:Copenhagen University Hospital Rigshospitalet | |||||||||||||
Full Title: A Randomized double-blind study of testosterone replacement therapy or placebo in testicular cancer survivors with mild Leydig Cell Insufficiency (Einstein-intervention) | |||||||||||||
Medical condition: Leydig Cell dysfunction | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003560-31 | Sponsor Protocol Number: UKM18_0021 | Start Date*: 2020-01-29 | |||||||||||
Sponsor Name:Universitätsklinikum Münster | |||||||||||||
Full Title: A prospective multicenter phase 2 study of copanlisib in combination with rituximab and CHOP chemotherapy (COPA-R-CHOP) in patients with previously untreated diffuse large B-cell lymphoma (DLBCL) | |||||||||||||
Medical condition: diffuse large B-cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005465-19 | Sponsor Protocol Number: DSC/06/2357/21 | Start Date*: 2007-02-09 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Open label, uncontrolled, pilot, phase II study of histone-deacetylase inhibitor ITF2357 administered orally to subjects with chronic lynphocytic leukemia (CLL) refractory/relapsed after convention... | |||||||||||||
Medical condition: Chronic lynphocytic leukemia (CLL) refractory/relapsed after conventional chemotherapy or relapsed after autologous bone marrow transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004167-22 | Sponsor Protocol Number: PGT307 | Start Date*: 2008-01-23 | |||||||||||||||||||||
Sponsor Name:Cell Therapeutics, Inc. | |||||||||||||||||||||||
Full Title: Paclitaxel poliglumex (CT-2103)/Carboplatin vs Paclitaxel/Carboplatin for the Treatment of Chemotherapy-Naive Advanced Non-Small Cell Lung Cancer (NSCLC) in Women with Estradiol > 30 pg/ml | |||||||||||||||||||||||
Medical condition: Advanced Non-small Cell Lung Cancer (NSCLC) in women. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004944-30 | Sponsor Protocol Number: AFX01-06 | Start Date*: 2006-02-23 | |||||||||||
Sponsor Name:Takeda Development Centre Europe Ltd | |||||||||||||
Full Title: An Open-Label Study to Investigate the Efficacy and Safety of AF37702 Injection in the Treatment of Anemia Caused by Antibody-Mediated Pure Red Cell Aplasia in Patients with Chronic Kidney Disease | |||||||||||||
Medical condition: Anemia caused by Antibody-Mediated Pure Red Cell Aplasia in Patients with Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001947-31 | Sponsor Protocol Number: TUD-CLL-X4-054 | Start Date*: 2013-02-27 | |||||||||||
Sponsor Name:Technische Universität Dresen | |||||||||||||
Full Title: Ofatumumab Induction and Maintenance in Elderly Patients with Poor Risk CLL in the Context of Allogeneic Transplantation: CLLX4 Trial | |||||||||||||
Medical condition: Patients aged >55 years with a diagnosis of CLL according to WHO criteria confirmed by flow cytometry of peripheral blood or bone marrow and a poor-risk disease according to the EBMT CLL Transplan... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002998-11 | Sponsor Protocol Number: ENDO-RCA | Start Date*: 2014-11-14 | |||||||||||
Sponsor Name:Rigshospitalet, Capital Region Bloodbank 2034, Section for Transfusion Medicine | |||||||||||||
Full Title: Safety and efficacy of low-dose Iloprost administration and blood pressure target in addition to standard therapy, as compared to standard therapy alone, in post-cardiac- arrest-syndrome patients... | |||||||||||||
Medical condition: Cardiac Arrest | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003884-12 | Sponsor Protocol Number: EXTRAStudy | Start Date*: 2015-12-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PAPA GIOVANNI XXIII | |||||||||||||
Full Title: A pilot, prospective, randomized, open-label, blinded endpoint (PROBE) histopathology trial to assess the effects of ACE- inhibition therapy on glomerular proliferative lesions in patients with ext... | |||||||||||||
Medical condition: Extracapillary glomerulonephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010571-24 | Sponsor Protocol Number: VEG111109 | Start Date*: 2009-08-03 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||||||||||||||||||
Full Title: An open label, multicenter, Phase I/II study of pazopanib in combination with paclitaxel in first line treatment of subjects with stage IIIBwet/IV non-small cell lung cancer | ||||||||||||||||||
Medical condition: Part I: Subjects with histologically or cytologically confirmed diagnosis of advanced solid tumours for which there is no standard therapy or for whom paclitaxel is standard therapy. Part II: Sta... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002144-42 | Sponsor Protocol Number: VEG111128 | Start Date*: 2009-05-26 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline R&D Limited | ||||||||||||||||||
Full Title: A Phase II, randomised, multicentre study to evaluate the efficacy and safety of pazopanib in combination with pemetrexed versus cisplatin plus pemetrexed, as first-line therapy in subjects with st... | ||||||||||||||||||
Medical condition: Histologically- or cytologically-confirmed diagnosis of non-predominantly squamous cell Stage IIIBwet (with confirmed malignant pleural effusion) or Stage IV NSCLC | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) DK (Completed) IT (Completed) NL (Completed) FR (Completed) ES (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006114-14 | Sponsor Protocol Number: 62326B1658 | Start Date*: 2012-04-17 |
Sponsor Name:Research and Development department | ||
Full Title: “Effects of testosterone on glycaemic control and other Cardiovascular Risk factors in Hypogonadal Men with uncontrolled Type 2 Diabetes: A randomized double – blinded placebo controlled add on tr... | ||
Medical condition: Hypogonadism Type 2 Diabetes Cardiovascular risk | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005602-26 | Sponsor Protocol Number: FL-101-2001 | Start Date*: 2021-08-03 | ||||||||||||||||||||||||||
Sponsor Name:Flame Biosciences | ||||||||||||||||||||||||||||
Full Title: A Two-cohort, Phase 2 Study of FL-101 as Neoadjuvant Therapy in Patients with Surgically Resectable Non-Small Cell Lung Cancer | ||||||||||||||||||||||||||||
Medical condition: Surgically resectable non-small cell lung cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000589-31 | Sponsor Protocol Number: NEMESIS | Start Date*: 2018-02-02 | ||||||||||||||||
Sponsor Name:SOCIETà CAMPANA DI IMMUNOTERAPIA ONCOLOGICA | ||||||||||||||||||
Full Title: multi stage phase II trial of Nivolumab (an anti –PD-1) in patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
Medical condition: patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004117-24 | Sponsor Protocol Number: GETUG-AFU26 | Start Date*: 2015-12-24 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A Phase II Safety Trial of Nivolumab in Patients with Metastatic Renal Cell Carcinoma Who Have Progressed During or After Prior Systemic Anti-Angiogenic Regimen | |||||||||||||
Medical condition: Patients suffering from refractory metastatic Renal Cell Carcinoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005825-12 | Sponsor Protocol Number: PB-06-002 | Start Date*: 2009-06-04 | |||||||||||
Sponsor Name:Protalix Biotherapeutics | |||||||||||||
Full Title: Ensayo clinico de fase 3, multicéntrico, en abierto y con cambio de tratamiento para evaluar la seguridad y eficacia de Glucocerebrosidasa Humana Recombinante expresada en células vegetales (prGCD)... | |||||||||||||
Medical condition: Enfermedad de Gaucher Gaucher Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) IT (Completed) DE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
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