- Trials with a EudraCT protocol (35)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (537)
35 result(s) found for: Cyclophosphamid.
Displaying page 1 of 2.
| EudraCT Number: 2005-000490-21 | Sponsor Protocol Number: SUCCESS | Start Date*: 2005-08-24 |
| Sponsor Name:1. Frauenklinik der LMU- Innenstadt | ||
| Full Title: Simultaneous Study of Gemcitabine-Docetaxel Combination adjuvant treatment, as well as Extended Bisphosphonate and Surveillance-Trial SUCCESS-Trial | ||
| Medical condition: This is an open-label, multicenter, 2x2 factorial design, randomized controlled, Phase III study comparing the time to recurrence after randomisation in patients with early primary breast cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003902-27 | Sponsor Protocol Number: 26866138MMY2031 | Start Date*: 2006-02-13 | |||||||||||
| Sponsor Name:ORTHO BIOTECH, Division of JANSSEN-CILAG GmbH | |||||||||||||
| Full Title: Clinical trial on induction of remission with bortezomib (Vel), cyclophosphamide (C) and dexamethasone (D) in patients until the age of 60 with untreated multiple myeloma and planned high dosage ch... | |||||||||||||
| Medical condition: Untreated patients with cytologically and/or histologically established multiple myeloma (Durie and Salmon stage II or III) requiring treatment with measurable myeloma protein in the blood or urine. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001094-29 | Sponsor Protocol Number: SUCCESS-B-Trail | Start Date*: 2008-04-14 |
| Sponsor Name:Klinikum der LMU | ||
| Full Title: Simultaneous Study of Gemcitabine-Docetaxel Combination adjuvant treatment, as well as Biological Targeted Treatment SUCCESS B-Trial | ||
| Medical condition: Patientinnen mit primärem epithelialem invasivem Mammakarzinom | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-002331-89 | Sponsor Protocol Number: MeCyTax | Start Date*: 2007-10-19 |
| Sponsor Name:Universität Magdeburg, Medizinische Fakultät | ||
| Full Title: Randomisierte Phase II Studie zur Therapieoptimierung der Behandlung des hormonrefraktären Prostatakarzinoms mit Docetaxel + Prednison versus Docetaxel + Prednison + low dose Cyclophosphamid | ||
| Medical condition: In dieser randomisierten Phase-II-Studie soll die Wirksamkeit und Toxizität einer 3-wöchentlichen Applikation von Docetaxel-Prednison und metronomisch applizierten Cyclophosphamid bei Patienten mit... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001075-37 | Sponsor Protocol Number: TUD-FHCRCD-010 | Start Date*: 2007-05-18 |
| Sponsor Name:University of Technology Dresden | ||
| Full Title: A Multi-center Phase III Study Comparing Myeloablative to Nonmyeloablative Transplantation in Patients with Myelodysplastic Syndrome or Acute Myelogenous Leukemia. | ||
| Medical condition: MDS and AML are predominantly diseases of older patients. For patients with advanced or chemotherapy refractory disease HCT is currently the only strategy that offers curative therapy. Unfortunat... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000967-24 | Sponsor Protocol Number: HED-324-PAE-0090-I | Start Date*: 2005-12-30 | |||||||||||
| Sponsor Name:Technical University of Munich | |||||||||||||
| Full Title: Evaluation of Response Rate to Pre-operative Docetaxel + Herceptin study part A and Docetaxel study part B In Locally Advanced Breast Cancer Patients, Stratified by HER2-Status, Trial Phase II | |||||||||||||
| Medical condition: therapeutic principles of primary systemic (=neo adjuvant) chemotherapy. In addition to the increased number of breast conserving operations, that could be already achieved by partially remission,... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003829-16 | Sponsor Protocol Number: RV-MM-DSMM-0279 | Start Date*: 2009-09-15 | |||||||||||
| Sponsor Name:GMIHO - Gesellschaft für medizinische Innovation Hämatologie und Onkologie mbH | |||||||||||||
| Full Title: An open, randomized clinical phase I/II trial to investigate maximum tolerated dose, efficacy, and safety of lenalidomide/low-dose dexamethasone in combination with continuous oral cyclophosphamide... | |||||||||||||
| Medical condition: relapsed multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000871-41 | Sponsor Protocol Number: STOPIgAN | Start Date*: 2008-01-24 | |||||||||||
| Sponsor Name:RWTH Aachen | |||||||||||||
| Full Title: Supportive versus Immunosuppressive Therapy for the treatment Of Progressive IgA Nephropathy | |||||||||||||
| Medical condition: IgA nephropathy (IgAN) as the most common type of glomerulonephritis. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003683-54 | Sponsor Protocol Number: OSHO #76 | Start Date*: 2008-06-18 |
| Sponsor Name:GMIHO Gesellschaft für medizinische Innovation/Hämatologie und Onkologie mbH | ||
| Full Title: Prospektive, offene, randomisierte, multizentrische Studie zur Effektivität von Palifermin in der Prophylaxe der Mukositis nach allogener Stammzelltransplantation mit myeloablativer Granzkörperbest... | ||
| Medical condition: Patients suffering from leukemia (acute or chronic), receiving allogenic blood stem cell transplantation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004970-24 | Sponsor Protocol Number: NHL-14 | Start Date*: 2008-01-17 | |||||||||||
| Sponsor Name:AGMT - Arbeitsgemeinschaft Medikamentöse Tumortherapie Gemeinnützige GmbH | |||||||||||||
| Full Title: Multizentrische Studie über die Cardiotoxizität von R-CHOP (Rituximab, Cyclophosphamid, Doxorubicin, Vincristin und Prednisolon) v. R-COMP (Rituximab, Cyclophosphamid, liposomalem Doxorubicin, Vinc... | |||||||||||||
| Medical condition: Diffus großzelliges B-Zell Lymphom | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011113-25 | Sponsor Protocol Number: SA2009 | Start Date*: 2009-05-29 | |||||||||||
| Sponsor Name:Per Honore | |||||||||||||
| Full Title: Populationsbaseret farmakokinetisk og farmakodynamisk doseringsmodel af epirubicin, cyklofosfamid og docetaxel til brystkræft | |||||||||||||
| Medical condition: brystcancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-005244-28 | Sponsor Protocol Number: GPOH-HD 2002 Pilot / VECOPA | Start Date*: 2005-05-19 |
| Sponsor Name:Universität Leipzig | ||
| Full Title: Pilotstudie zur Therapieoptimierungsstudie für den Morbus Hodgkin bei Kindern und Jugendlichen Prüfung der Verträglichkeit der Chemotherapiekombination VECOPA bei Patienten der Therapiegruppen 2 ... | ||
| Medical condition: Pilotstudie zur Therapieoptimierungsstudie für den Morbus Hodgkin bei Kindern und Jugendlichen Prüfung der Verträglichkeit der Chemotherapiekombination VECOPA bei Patienten der Therapiegruppen 2 ... | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-009874-28 | Sponsor Protocol Number: ABCSG-34; GA6182EI | Start Date*: 2009-06-26 |
| Sponsor Name:ABCSG - Austrian Breast & Colorectal Cancer Study Group | ||
| Full Title: Epirubicine plus Cyclophosphamid followed by Docetaxel +/- Sunitinib before surgery for the treatment of patients with HER2neu-negative operable breast cancer | ||
| Medical condition: HER2neu-negative operable breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002546-11 | Sponsor Protocol Number: HAN-HCC-002 | Start Date*: 2006-10-20 | |||||||||||
| Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
| Full Title: Offene Phase IIIb Studie zur Elimination von CD4+CD25+ regulatorischen T-Zellen bei Patienten mit fortgeschrittenem HCC durch die Gabe von Cyclophosphamid | |||||||||||||
| Medical condition: Fortgeschrittenes Leberzellkarzinom | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003920-30 | Sponsor Protocol Number: CHARLY | Start Date*: 2016-09-20 |
| Sponsor Name:University Hospital Heidelberg | ||
| Full Title: Phase-II study on the value of post-transplant Cyclophosphamide after Thiotepa-based haplo-identical stem-cell transplantation for relapsed-refractory lymphoma | ||
| Medical condition: Myeloablative haplo-identical stem cell transplantation for poor risk non-hodgkin lymphoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-003064-19 | Sponsor Protocol Number: NeoTEC | Start Date*: 2008-12-30 | |||||||||||
| Sponsor Name:Universität Leipzig | |||||||||||||
| Full Title: Phase-IIb-Study to Evaluate the Effect of a Neoadjuvant Chemotherapy with Docetaxel, Epirubicine and Cyclphosphamide (TEC) in Patients with primary HER-2 neu Negative Mammacarcinoma | |||||||||||||
| Medical condition: Primary mamma carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005069-60 | Sponsor Protocol Number: P000798 | Start Date*: 2015-05-26 |
| Sponsor Name:Medical Center - University of Freiburg | ||
| Full Title: R-CPOP as first line therapy for elderly patients with DLBCL and for patients with limited cardiac function with DLBCL | ||
| Medical condition: Diffuse-large B cell lymphoma (DLBCL) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-005034-36 | Sponsor Protocol Number: KWI-300-104 | Start Date*: 2008-07-15 | |||||||||||
| Sponsor Name:Apotex Inc. | |||||||||||||
| Full Title: A non comparative, multicentre, repeat dose safety in use study of Neukine® (Filgrastim) in patients receiving chemotherapy known to induce neutropenia | |||||||||||||
| Medical condition: Febrile neutropenia in breast cancer patients undergoing TAC chemotherapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: HU (Completed) AT (Completed) PL (Completed) BG (Completed) GR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005217-38 | Sponsor Protocol Number: DSHNHL2004-2 | Start Date*: 2008-07-25 | |||||||||||
| Sponsor Name:German High Grade Non-Hodgkins Lymphoma group | |||||||||||||
| Full Title: Randomiseret forsøg der sammenligner 4 og 6 kemoterapicykler med CHOP (Cyklofosfamid, Doxorubicin, Vincristin og Prednison) i 21-dages intervaller, begge med 6 cykler immunterapi med monoklonalt an... | |||||||||||||
| Medical condition: Patients with untreated aggressive CD20+ Non-Hodgkins Lymphoma aged 18 to 60 years without major accompanying disorders with no risk factor according to IPI and no bulky disease (<7,5cm) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012758-18 | Sponsor Protocol Number: COALL09-05-04 | Start Date*: 2010-09-09 | |||||||||||
| Sponsor Name:Universitätsklinikum Hamburg-Eppendorf | |||||||||||||
| Full Title: A randomized multi-center treatment study (COALL 08-09) to improve the survival of children with acute lymphoblastic leukemia on behalf of the German Society of Pediatric Hematology and Oncology | |||||||||||||
| Medical condition: acute lymphoblastic leukemia in children and adolescents 1 to ≤ 18 years of age | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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