- Trials with a EudraCT protocol (41)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
41 result(s) found for: Sexual differentiation.
Displaying page 1 of 3.
EudraCT Number: 2009-012807-25 | Sponsor Protocol Number: IIL-MCL0208 | Start Date*: 2010-01-28 | ||||||||||||||||||||||||||
Sponsor Name:IIL INTERGRUPPO ITALIANO LINFOMI ONLUS | ||||||||||||||||||||||||||||
Full Title: A PHASE III MULTICENTER, RANDOMIZED STUDY WITH LENALIDOMIDE (Revlimid) MAINTENANCE VERSUS OBSERVATION AFTER INTENSIFIED INDUCTION REGIMEN CONTAINING RITUXIMAB FOLLOWED BY HIGH DOSE CHEMOTHERAPY A... | ||||||||||||||||||||||||||||
Medical condition: Mantel cell lymphoma | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) PT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005439-41 | Sponsor Protocol Number: PLRG-10/ML29157 | Start Date*: 2017-08-13 | |||||||||||
Sponsor Name:Polish Lymphoma Research Group (PLRG) | |||||||||||||
Full Title: EVALUATION OF EFFICACY AND SAFETY OF OBINUTUZUMAB PREEMPTIVE TREATMENT AT THE TIME OF THE MOLECULAR RELAPSE AFTER FIRST LINE IMMUNOCHEMOTHERAPY WITH AUTOLOGOUS STEM CELL TRANSPLANTATION IN MANTLE C... | |||||||||||||
Medical condition: Molecular relapse after the first line immunochemotherapy with autologous stem cell transplantation in mantle cell lymphoma (MCL) patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000044-14 | Sponsor Protocol Number: LEN DEX MCL 07 | Start Date*: 2008-10-22 | |||||||||||
Sponsor Name:IIL INTERGRUPPO ITALIANO LINFOMI ONLUS | |||||||||||||
Full Title: SALVAGE TREATMENT WITH LENALIDOMIDE AND DEXAMETHASONE (LEN-DEX) IN PATIENTS WITH RELAPSED/REFRACTORY MANTLE CELL LYMPHOMA (MCL) | |||||||||||||
Medical condition: Treatment of patients with MCL relapsed or refractory to at least one line of chemotherapy, not eligible for or relapsed after more intensive treatments. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001430-16 | Sponsor Protocol Number: 3066K1-305-WW | Start Date*: 2005-04-20 |
Sponsor Name:Wyeth Research, Division of Wyeth Pharmaceuticals, Inc. Clinical Research and Development | ||
Full Title: An Open-label, Randomized, Phase 3 Trial of intravenous Temsirolimus (CCI-779) at two Dose Levels Compared to Investigator's Choice Therapy in relapsed, Refractory Subjects with Mantle Cell lymphom... | ||
Medical condition: Mantle Cell Lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) SE (Completed) GB (Completed) DE (Completed) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-007756-34 | Sponsor Protocol Number: CC-5013-MCL-001 | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Phase 2, multicenter, single-arm, open-label study to determine the efficacy and safety of single-agent lenalidomide (Revlimid ®) in patients with mantle cell NHL who have relapsed or progressed ... | |||||||||||||
Medical condition: Mantle cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) AT (Completed) HU (Completed) FR (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006177-32 | Sponsor Protocol Number: CC-5013-MCL-003 | Start Date*: 2010-01-06 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE 3 MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, FIRST LINE MAINTENANCE STUDY OF LENALIDOMIDE (REVLIMID®) IN PATIENTS WITH MANTLE-CELL LYMPHOMA | |||||||||||||
Medical condition: Mantle-Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) FR (Completed) DE (Completed) ES (Completed) PT (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002542-20 | Sponsor Protocol Number: MCLR2elderly | Start Date*: 2013-05-21 | |||||||||||
Sponsor Name:LYSARC | |||||||||||||
Full Title: Efficacy of alternating immunochemotherapy consisting of R-CHOP + R-HAD versus R-CHOP alone, followed by maintenance therapy consisting of additional lenalidomide with rituximab versus rituximab al... | |||||||||||||
Medical condition: Mantle Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) DE (Ongoing) NL (Completed) PT (Completed) ES (Ongoing) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005299-26 | Sponsor Protocol Number: 54767414LYM2001 | Start Date*: 2015-06-08 | |||||||||||||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||||||||||||
Full Title: An Open Label, Phase 2 Study to Evaluate Efficacy and Safety of Daratumumab in Relapsed or Refractory Mantle Cell Lymphoma, Diffuse Large B-Cell Lymphoma, and Follicular Lymphoma | |||||||||||||||||||||||
Medical condition: Relapsed or Refractory Mantle Cell Lymphoma, Diffuse Large B-Cell Lymphoma, and Follicular Lymphoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001060-38 | Sponsor Protocol Number: NLG-MCL7 | Start Date*: 2018-02-21 | |||||||||||
Sponsor Name:Nordic Lymphoma Group | |||||||||||||
Full Title: Venetoclax, lenalidomide and rituximab in patients with relapsed/refractory mantle cell lymphoma. | |||||||||||||
Medical condition: Relapsed/refractory mantle cell lymphoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) NO (Completed) DK (Ongoing) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011513-24 | Sponsor Protocol Number: CC-5013-MDS-005 | Start Date*: 2009-12-14 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO COMPARE THE EFFICACY AND SAFETY OF LENALIDOMIDE (REVLIMID®) VERSUS PLACEBO IN SUBJECTS WITH TRANSFUSION... | |||||||||||||
Medical condition: TRANSFUSION-DEPENDENT ANEMIA DUE TO IPSS LOW OR INTERMEDIATE-1 RISK MYELODYSPLASTIC SYNDROMES WITHOUT DELETION 5Q [31] AND UNRESPONSIVE OR REFRACTORY TO ERYTHROPOIESIS-STIMULATING AGENT | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) FR (Completed) CZ (Completed) AT (Completed) IT (Completed) PT (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001574-28 | Sponsor Protocol Number: AT13387-04 | Start Date*: 2012-10-09 | |||||||||||
Sponsor Name:Astex Pharmaceuticals Inc | |||||||||||||
Full Title: A Phase 2 Study of Hsp90 Inhibitor AT13387 Alone or in Combination with Abiraterone Acetate in the Treatment of Castration-Resistant Prostate Cancer (CRPC) no Longer Responding to Abiraterone | |||||||||||||
Medical condition: Castration-Resistant Prostate Cancer (CRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004223-36 | Sponsor Protocol Number: RI-01-006 | Start Date*: 2019-09-23 | |||||||||||
Sponsor Name:Dr. Reddy’s Laboratories S.A. | |||||||||||||
Full Title: A Randomised, Double-blind, Parallel-group, Phase III Study to Compare the Efficacy, Safety, and Immunogenicity of Proposed Rituximab Biosimilar (DRL_RI) with MabThera® in Subjects with Previously ... | |||||||||||||
Medical condition: Follicular Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) ES (Ongoing) CZ (Completed) BG (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
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: 2013-004711-50 | Sponsor Protocol Number: 9785-MA-1001 | Start Date*: 2014-11-24 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase IIIb Study of the Efficacy and Safety of Continuing Enzalutamide in Chemotherapy Naïve Metastatic Castration Resistant Prostate Cancer Patients... | |||||||||||||
Medical condition: Metastatic Castrate Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) IT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) SE (Prematurely Ended) ES (Prematurely Ended) GR (Completed) BE (Completed) FR (Completed) AT (Ongoing) PL (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002154-23 | Sponsor Protocol Number: UKM_04_12_TCP_ATRA_AML | Start Date*: 2014-08-28 | |||||||||||
Sponsor Name:Martin-Luther-University Halle-Wittenberg | |||||||||||||
Full Title: Phase I/II pilot trial of ATRA (Tretinoin) and TCP (Tranylcypromine) in patients with relapsed or refractory acute myeloid leukemia (AML) when no intensive treatment is possible | |||||||||||||
Medical condition: relapse or refractory AML in patients unfit for an intensive treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023382-22 | Sponsor Protocol Number: 9521-CL-0002 | Start Date*: 2011-02-21 | ||||||||||||||||
Sponsor Name:Astellas Pharma Europe B.V. (APEB) | ||||||||||||||||||
Full Title: Phase I/II, multi-center, open label study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics and anti-tumor activity of ASP9521 in patients with metastatic castrate-resistant p... | ||||||||||||||||||
Medical condition: metastatic castrate-resistant prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003597-10 | Sponsor Protocol Number: MK-8591A-028 | Start Date*: 2020-07-15 | |||||||||||
Sponsor Name:MERCK SHARP & DOHME CORP. UNA SUSSIDIARIA DI MERCK & CO. INC. | |||||||||||||
Full Title: A Phase 2 Clinical Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Doravirine/Islatravir in Adolescents with HIV-1 Infection who are Virologically Suppressed, are >=12 to <18 Years ... | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001725-26 | Sponsor Protocol Number: X-CGD-Version2 | Start Date*: 2013-03-12 | |||||||||||
Sponsor Name:Johann Wolfgang Goethe-University | |||||||||||||
Full Title: A Phase I/II Gene Therapy trial for X-CGD with a SIN gamma retroviral vector | |||||||||||||
Medical condition: Chronic granulomatous disease (CGD) is a congenital immunodeficiency, in which neutrophil granulocytes and monocytes are not capable of producing reactive oxygen species and therefore are unable to... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000590-23 | Sponsor Protocol Number: MK-8591A-020 | Start Date*: 2020-03-31 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck &Co.,Inc | |||||||||||||
Full Title: A Phase 3 Randomized, Active-Controlled, Double-Blind Clinical Study to Evaluate the Antiretroviral Activity, Safety, and Tolerability of Doravirine/Islatravir Once-Daily in HIV-1 Infected Treatm... | |||||||||||||
Medical condition: HIV-1 infection and naïve to antiretroviral therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002932-18 | Sponsor Protocol Number: 42756493-BLC3001 | Start Date*: 2018-02-08 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 3 Study of Erdafitinib Compared with Vinflunine or Docetaxel or Pembrolizumab in Subjects with Advanced Urothelial Cancer and Selected FGFR Gene Aberrations | |||||||||||||
Medical condition: Advanced Urothelial Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Trial now transitioned) HU (Completed) ES (Ongoing) AT (Completed) FR (Trial now transitioned) DE (Ongoing) NL (Ongoing) PT (Completed) GR (Completed) PL (Completed) IT (Completed) DK (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
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