- 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 2 of 6.
EudraCT Number: 2004-004545-18 | Sponsor Protocol Number: NA | Start Date*: 2005-04-26 |
Sponsor Name:CHU Sart Tilman | ||
Full Title: Cell therapy for cardiac repair through mobilization of hematopoietic stem cells and endothelial progenitors in patients with chronic ischemic cardiomyopathy. | ||
Medical condition: Chronic ischemic cardiac disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-003784-68 | Sponsor Protocol Number: 4 | Start Date*: 2005-04-05 |
Sponsor Name:University Hospital Bern | ||
Full Title: Subcutanoeus Delivery of Filgrastim (rG-CSF) for the Promotion of Collateral Growth in Patients with Coroanry Artery Disease (FILCAD) | ||
Medical condition: Coronary Artery Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004646-13 | Sponsor Protocol Number: 670/05 | Start Date*: 2005-11-17 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: PEG-Filgrastim versus Filgrastim as an adjunct to therapy CHOP-14 Rituximab in elderly patients 60-75 years old with B cell non-Hodgkin s High/intermediate grade lymphoma. A randomized, prospe... | |||||||||||||
Medical condition: Maintenance of dose-intensity | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002136-10 | Sponsor Protocol Number: GRIFO-A | Start Date*: 2005-07-08 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Comparison between once-per-cycle peg-Filgrastim and daily injection r-Hu-G-CSF in chemotherapy-induced neutropenia treatment and peripheral blood progenitor cells mobilization in childhood. | |||||||||||||
Medical condition: chemotherapy-induced neutropenia treatment peripheral blood progenitor cells mobilization | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001741-14 | Sponsor Protocol Number: TEM-MM-101 | Start Date*: 2018-12-13 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: A phase I/II dose escalation study evaluating safety and activity of autologous CD34+-enriched hematopoietic progenitor cells genetically modified with a lentiviral vector encoding for the human in... | |||||||||||||
Medical condition: Multiple myeloma in early relapse after intensive front line therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002228-28 | Sponsor Protocol Number: STEMALS-II | Start Date*: 2014-09-01 |
Sponsor Name:Università degli Studi di Torino e Azienda Ospedaliera Città della Salute e della Scienza di Torino | ||
Full Title: A double blind, placebo controlled, parallel groups, multicenter study on filgrastim in amyotrophic lateral sclerosis | ||
Medical condition: Amyotrophic lateral sclerosis (ALS) is a severe progressive neurological disorder characterized by a selective degeneration of spinal, bulbar, and cortical motor neurons. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002429-37 | Sponsor Protocol Number: NSGO-EC-9501 Amendment 2 | Start Date*: 2004-11-17 |
Sponsor Name:Nordic Society for Gynecologic Oncology | ||
Full Title: A randomized trial of adjuvant treatment with radiation plus chemotherapy versus radiation alone in high-risk endometrial carcinoma NSGO-EC-9501 Amendment 2. | ||
Medical condition: Endometrial cancer stage I-III radically operated with high-risk factors (high-grade and deep myometrial infiltration, or serous or clear cell histology) that will receive adjuvant treatment with r... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001113-18 | Sponsor Protocol Number: GCSFEPO_01 | Start Date*: 2006-02-14 |
Sponsor Name:Universitätsklinikum Münster | ||
Full Title: Beeinflussung assoziativen Lernens und motorischer Fähigkeiten durch G-CSF und EPO | ||
Medical condition: Amyotrophische Lateralsklerose Chronischer Schlaganfall | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-014721-16 | Sponsor Protocol Number: IRRB/19/09 | Start Date*: 2009-11-18 |
Sponsor Name:ISTITUTO MEDITERRANEO PER I TRAPIANTI E TERAPIE AD ALTA SPECIALIZZAZIONE | ||
Full Title: Controlled randomized pilot study for characterization and identification of CD34+ stem cells in the splancnic distrect after GCSF stimolation in cirrhotic patients | ||
Medical condition: Liver cirrhosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-001152-39 | Sponsor Protocol Number: SSG XX | Start Date*: 2024-05-21 |
Sponsor Name:Scandinavian Sarcoma Group | ||
Full Title: SSGXX A Scandinavian Sarcoma Group treatment protocol for adult patients with non-metastatic high-risk soft tissue sarcoma of the extremities and trunk wall | ||
Medical condition: SSG XX is a phase II trial for high-risk soft tissue sarcoma(STS) of the extremities and trunk wall. Prognostic markers are used to identify high-risk tumors. SSG XX will evaluate chemo-and radioth... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003096-20 | Sponsor Protocol Number: CDF711 | Start Date*: 2005-09-06 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Use of peg-filgrastim in severe chronic neutropenia | |||||||||||||
Medical condition: severe chronic neutropenia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001051-39 | Sponsor Protocol Number: FMG-MM-02 | Start Date*: 2012-11-15 | |||||||||||
Sponsor Name:Kuopio University Hospital, Clinic of Internal Medicine/Center of Medicine | |||||||||||||
Full Title: A prospective phase II study to assess immunophenotypic remission after three-drug in-duction followed by randomized stem cell mobilization, autologous stem cell transplantation and lenalidomide ma... | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004498-29 | Sponsor Protocol Number: 20190360 | Start Date*: 2022-01-13 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: Phase 3 Randomized, Controlled Study of Blinatumomab Alternating With Low-intensity Chemotherapy Versus Standard of Care for Older Adults With Newly Diagnosed Philadelphia-negative B-cell Precursor... | |||||||||||||
Medical condition: Newly Diagnosed Philadelphia (Ph)-negative B-cell Precursor Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PT (Trial now transitioned) SE (Trial now transitioned) AT (Trial now transitioned) FI (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) DK (Trial now transitioned) IT (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) NL (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024481-22 | Sponsor Protocol Number: EP06-302 | Start Date*: 2012-01-17 | |||||||||||
Sponsor Name:Sandoz GmbH | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, multi-center Phase III study comparing the efficacy and safety of EP2006 and Neupogen® in breast cancer patients treated with myelosuppressive chemothe... | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) SK (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002697-45 | Sponsor Protocol Number: ACT15378 | Start Date*: 2019-03-04 | ||||||||||||||||
Sponsor Name:Sanofi-aventis recherche & developpement | ||||||||||||||||||
Full Title: Open-label, Single-arm Trial to Evaluate Antitumor Activity, Safety, and Pharmacokinetics of Isatuximab Used in Combination With Chemotherapy in Pediatric Patients From 28 Days to Less Than 18 Year... | ||||||||||||||||||
Medical condition: Open-label, Single-arm Trial to Evaluate Antitumor Activity, Safety, and Pharmacokinetics of Isatuximab Used in Combination with Chemotherapy in Pediatric Patients from 28 Days to Less than 18 Year... | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) NO (Completed) FI (Completed) DK (Completed) FR (Completed) NL (Completed) PT (Completed) BE (Completed) DE (Completed) CZ (Completed) GR (Completed) Outside EU/EEA IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003544-83 | Sponsor Protocol Number: 69HCL19_0375 | Start Date*: 2021-03-16 | ||||||||||||||||
Sponsor Name:Hospices Civils de Lyon - Direction de la Recherche Clinique | ||||||||||||||||||
Full Title: Evaluation de l’efficacité thérapeutique du filgrastim dans les allergies sévères bulleuses aux médicaments s’exprimant sous forme de Lyell et Stevens-Johnson Etude GNET | ||||||||||||||||||
Medical condition: Syndrome de Stevens Johnson (SJS) Syndrome de Lyell (NET) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002545-30 | Sponsor Protocol Number: IRAS220495 | Start Date*: 2017-11-06 | |||||||||||
Sponsor Name:Barts Health NHS Trust | |||||||||||||
Full Title: Autologous Stem cell Transplantation In refractory Crohn's disease - Low Intensity Therapy Evaluation | |||||||||||||
Medical condition: Refractory Crohn's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007161-20 | Sponsor Protocol Number: BK0023-02C | Start Date*: 2009-01-08 | |||||||||||
Sponsor Name:BIO-KER S.R.L | |||||||||||||
Full Title: Comparable efficacy and safety profiles of daily injection of BK0023 and filgrastim (Neupogen®) in chemotherapy-induced neutropenia: a multinational, multicenter, investigator blind, randomised, pa... | |||||||||||||
Medical condition: Chemotherapy induced Neutropenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003399-36 | Sponsor Protocol Number: MK-4214-008 | Start Date*: 2011-10-28 | |||||||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||||||||||||
Full Title: A Phase III Randomized, Double-Blind, Active-Controlled Clinical Trial to Study the Efficacy and Safety of MK-4214 (filgrastim) and Neupogen™ as an Adjunct to Combination Chemotherapy with Doxorubi... | |||||||||||||||||||||||
Medical condition: Breast Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000700-14 | Sponsor Protocol Number: R-HDS 0305 | Start Date*: 2005-04-12 |
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALI RIUNITI DI BERGAMO A.O. DI RILIEVO NAZIONALE | ||
Full Title: MULTI-CENTRE, RANDOMISED, PHASE III TRIAL COMPARING HIGH DOSE SEQUENTIAL CHEMOTHERAPY hds WITH RITUXIMAB AND AUTOLOGOUS PERIPHERAL BLOOD PROGENITUR ALL TRANSPLANTION VERSUS 2- WEEKLY CHOP WITH RI... | ||
Medical condition: ADULT PATIENTS WITH DIFFUSE LARGE B- CELL NON HODGKIN LYMPHOMA | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
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