- Trials with a EudraCT protocol (104)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
104 result(s) found for: Filgrastim.
Displaying page 4 of 6.
EudraCT Number: 2010-020772-38 | Sponsor Protocol Number: IRST 174.05 | Start Date*: 2010-09-13 | |||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
Full Title: A Phase II Study of Dose Density Regimen with Fluorouracil, Epirubicin and Cyclophosphamide at Days 1, 4 Every 14 Days with Filgrastim Support followed by Weekly Paclitaxel in Women with Primary Br... | |||||||||||||
Medical condition: Patients with primary breast cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001641-33 | Sponsor Protocol Number: PETAL-Studie | Start Date*: 2007-07-25 |
Sponsor Name:Universitätsklinikum Essen | ||
Full Title: Positronen-Emissionstomographie-gesteuerte Therapie aggressiver Non-Hodgkin-Lymphome (Positron emission tomography guided therapy of aggressive non-Hodgkin's lymphomas) | ||
Medical condition: Aggressive non-Hodgkin's lymphomas (first line therapy) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000563-25 | Sponsor Protocol Number: 2011/119/HP | Start Date*: 2012-07-27 | |||||||||||
Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||
Full Title: Randomized phase III study of gemcitabine and cisplatin (GC) versus high dose intensity methotrexate, vinblastine, doxorubicin and cisplatin (HD-MVAC) in the perioperative setting for patients with... | |||||||||||||
Medical condition: locally advanced transitional cell cancer of the bladder | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004540-29 | Sponsor Protocol Number: Pona-CELL | Start Date*: 2020-10-06 | |||||||||||
Sponsor Name:Ústav hematologie a krevní transfuze | |||||||||||||
Full Title: Ponatinib plus reduced-intensity chemotherapy in the first-line treatment of adult patients with Ph-positive acute lymphoblastic leukemia | |||||||||||||
Medical condition: NEWLY DIAGNOSED PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002654-95 | Sponsor Protocol Number: NET-MS | Start Date*: 2023-04-17 | ||||||||||||||||
Sponsor Name:FONDAZIONE ITALIANA SCLEROSI MULTIPLA ONLUS | ||||||||||||||||||
Full Title: No Evidence Of Disease Activity After Autologous Haematopoietic Stem Cell Transplantation In Aggressive Multiple Sclerosis | ||||||||||||||||||
Medical condition: Relapsing Remitting Multiple Sclerosis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000971-15 | Sponsor Protocol Number: PLERIFLAG | Start Date*: 2011-09-23 | |||||||||||
Sponsor Name:PETHEMA | |||||||||||||
Full Title: Multicentric, prospective, open-label, of one group and phase I-II clinical trial to analyze induction treatment with a combination of fludarabine, idarubicin, cytarabine, G-CSF and plerixafor for ... | |||||||||||||
Medical condition: Relapsed or resistant acute myeloid leukemia (AML). | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001549-42 | Sponsor Protocol Number: STH19379 | Start Date*: 2020-03-27 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals | |||||||||||||
Full Title: A multicentre, randomised controlled trial to evaluate the efficacy of autologous haematopoietic stem cell transplantation versus alemtuzumab or ocrelizumab in relapsing remitting multiple sclerosis. | |||||||||||||
Medical condition: Highly active relapsing remitting multiple sclerosis | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004718-32 | Sponsor Protocol Number: NL72607.041.20 | Start Date*: 2020-10-09 |
Sponsor Name:UMC Utrecht | ||
Full Title: Upfront autologous hematopoietic stem cell transplantation versus immunosuppressive medication in early diffuse cutaneous systemic sclerosis: an international multicentre, open-label, randomized co... | ||
Medical condition: Diffuse cutaneous systemic sclerosis according to the ACR/EULAR criteria | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003337-40 | Sponsor Protocol Number: final version 2.0 | Start Date*: 2006-02-13 |
Sponsor Name:European Group for Blood and Marrow Transplantation (EMBT) | ||
Full Title: Autologous Stem Cell Transplantation for Crohn's Disease ('ASTIC'-Trial: Autologous Stem Cell Transplantation International Crohn's Disease Trial) | ||
Medical condition: Patients with Crohn's disease who have not responded to immunosupressant medication | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) IT (Ongoing) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012950-19 | Sponsor Protocol Number: GMALL-B-ALL/NHL 2002, NILG 2009 | Start Date*: 2009-10-30 | |||||||||||
Sponsor Name:NILG (Northern Italy Leukemia Group) | |||||||||||||
Full Title: Multicentre study to optimize therapy of B-ALL and high grade non-Hodgkin Lymphoma in Adults | |||||||||||||
Medical condition: Burkitt`s Lymphoma Burkitt`s Leukemia | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004885-18 | Sponsor Protocol Number: 1805/2004 | Start Date*: 2004-12-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Evaluation of febrile event during emopoietic progenitor cells aferesi post chemotherapy treatment in patients affected by multiple myeloma. | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021885-31 | Sponsor Protocol Number: N10TIL | Start Date*: 2011-03-24 | |||||||||||
Sponsor Name:NKI-AVL | |||||||||||||
Full Title: Randomized Phase II Study Using a Non-myeloablative Lymphocyte Depleting Regimen of Chemotherapy Followed by Infusion of Tumor Infiltrating Lymphocytes and Interleukin-2 in Metastatic Melanoma’ | |||||||||||||
Medical condition: Patients with metastatic (stage IV) melanoma will be randomized to either treatment arm A (dacarbazine) or treatment arm B (TIL) after metastasectomy and feasibility of culturing of TIL. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004398-41 | Sponsor Protocol Number: IJB-BC-TDM1BM-2016 | Start Date*: 2018-01-26 | ||||||||||||||||
Sponsor Name:Institut Jules Bordet | ||||||||||||||||||
Full Title: Multicentre, non-randomised, open-label, single agent phase II study to determine the clinical benefit of trastuzumab emtansine (T-DM1) in HER2-positive metastatic breast cancer patients with brain... | ||||||||||||||||||
Medical condition: Metastatic HER2-positive breast cancer with brain metastasis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) AT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-003599-39 | Sponsor Protocol Number: AMD3100-3102-DE | Start Date*: 2005-12-02 | |||||||||||
Sponsor Name:AnorMED Corp. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, comparative trial of AMD3100 (240 mcg/kg) plus G-CSF (10 mcg/kg) versus G-CSF (10 mcg/kg) plus placebo to mobilize and collect greater than or equal ... | |||||||||||||
Medical condition: Mobilization of stem cells prior to autologous stem cell transplantation in patients with multiple myeloma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001772-38 | Sponsor Protocol Number: G112 | Start Date*: 2013-06-29 | |||||||||||
Sponsor Name:A.N.M.C.O.-Fondazione Italiana lotta Malattie Cardiovasc | |||||||||||||
Full Title: STEM-AMI OUTCOME TRIAL STem cElls Mobilization in Acute Myocardial Infarction Outcome Trial | |||||||||||||
Medical condition: Patients with left ventricular systolic disfunction after revascularization for acute myocardial infarction | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000664-16 | Sponsor Protocol Number: FLATauto | Start Date*: 2008-02-26 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Clinical phase II trial to evaluate the safety and efficacy of treosulfan combined with cytarabine and fludarabine prior to autologous haematopoietic stem cell transplantation in elderly patients w... | |||||||||||||
Medical condition: elderly patients with Acute Myeloid Leukemia or Myelodysplastic Syndrome | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006390-37 | Sponsor Protocol Number: VX21-CTX001-161 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | ||||||||||||||||||
Full Title: A Phase 3b Study to Evaluate Efficacy and Safety of a Single Dose of Autologous CRISPR Cas9 Modified CD34+ Human Hematopoietic Stem and Progenitor Cells (CTX001) in Subjects with Transfusion-Depend... | ||||||||||||||||||
Medical condition: Transfusion-dependent β-thalassemia (TDT) and severe sickle cell disease (SCD) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002288-84 | Sponsor Protocol Number: RR3 | Start Date*: 2019-08-12 |
Sponsor Name:RenovoRx, Inc. | ||
Full Title: Targeted Intra-arterial Gemcitabine vs. Continuation of IV Gemcitabine plus Nab-Paclitaxel following Induction with sequential IV Gemcitabine plus Nab-Paclitaxel and Radiotherapy for Unresectable L... | ||
Medical condition: Locally advanced pancreatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001308-31 | Sponsor Protocol Number: PALG-AML1/2016 | Start Date*: 2017-06-27 |
Sponsor Name:Polish Adult Leukaemia Group (PALG) | ||
Full Title: A Polish Adult Leukemia Group (PALG) prospective, multicenter clinical trial to compare the efficacy of two standard induction therapies (DA-90 vs DAC) and two standard salvage regimens (FLAG-IDA ... | ||
Medical condition: The study will include newly diagnosed AML patients (other than acute promyelocytic leukemia); age 18-60 years, who are eligible for standard induction chemotherapy. The patients will be randomized... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005923-42 | Sponsor Protocol Number: TACL2008-002/ITCC033 | Start Date*: 2013-04-09 | ||||||||||||||||
Sponsor Name:TACL | ||||||||||||||||||
Full Title: A Phase I Trial of NECTAR (Nelarabine, Etoposide and Cyclophosphamide in T-ALL Relapse): A Joint Study of TACL, POETIC and ITCC | ||||||||||||||||||
Medical condition: relapsed T-ALL, T-NHL | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) AT (Prematurely Ended) GB (Completed) IT (Prematurely Ended) FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
