- Trials with a EudraCT protocol (79)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
79 result(s) found for: Pegfilgrastim.
Displaying page 1 of 4.
EudraCT Number: 2006-001409-27 | Sponsor Protocol Number: ONC-2006-001 | Start Date*: 2006-06-29 | |||||||||||
Sponsor Name:ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Pegfilgrastim versus filgrastim after high-dose chemotherapy followed by autologous peripheral blood stem cell, in patients with hematologic and solid tumors a randomized phase II study | |||||||||||||
Medical condition: Patients with hematological neoplasia or solid tumors treated with high-dose chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001005-26 | Sponsor Protocol Number: GECP 05-01 | Start Date*: 2005-09-07 |
Sponsor Name:Spanish Lung Cancer Group | ||
Full Title: A single-arm phase II study of dose-dense gemcitabine and carboplatin as neoadyuvant chemotherapy, with pegfilgrastim support for subjects with operable stage IIIA NSCLC | ||
Medical condition: Non-small cell lung cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2006-000891-34 | Sponsor Protocol Number: ERA2006001 | Start Date*: 2006-05-05 |
Sponsor Name:Hôpital Ambroise Paré | ||
Full Title: A randomized, international, open-label, phase II study of peripheral blood progenitor cell (PBPC) mobilization and engraftment with pegfilgrastim or filgrastim for autologous transplantation in su... | ||
Medical condition: Multiple Myeloma . | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004321-95 | Sponsor Protocol Number: AMLSG 07-04 | Start Date*: 2005-05-26 |
Sponsor Name:University of Ulm | ||
Full Title: RANDOMIZED PHASE II-STUDY ON VALPROIC ACID, ALL-TRANS RETINOIC ACID AND THEIR COMBINATION IN INDUCTION AND CONSOLIDATION THERAPY AS WELL AS PEGFILGRASTIM AFTER CONSOLIDATION THERAPY IN YOUNGER PATI... | ||
Medical condition: newly diagnosed acute myeloid leukemia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003469-24 | Sponsor Protocol Number: SPI-GCF-302 | Start Date*: 2017-03-14 | |||||||||||
Sponsor Name:Spectrum Pharmaceuticals, Inc. | |||||||||||||
Full Title: Randomized, OpEn-Label, Active-ContrOl Trial of SPI-2012 (Eflapegrastim) Versus Pegfilgrastim in the Management of Chemotherapy-Induced Neutropenia in Early-Stage BReast Cancer Patients Receiving D... | |||||||||||||
Medical condition: Management of Neutropenia in Patients with Breast Cancer who receiving Chemotherapy with the Docetaxel + Cyclophosphamide | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000266-64 | Sponsor Protocol Number: PEGF/USV/P3/003 | Start Date*: 2015-06-18 | ||||||||||||||||
Sponsor Name:USV Limited | ||||||||||||||||||
Full Title: A Randomised, Multi-Centre, Assessor-Blinded, Active-Controlled, Parallel Group, Equivalence Phase III Study Comparing the Safety and Efficacy of USV Pegfilgrastim and Neulasta® in Breast Cancer Pa... | ||||||||||||||||||
Medical condition: Duration of Sever Neutropenia and incidence of febrile neutropenia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: HU (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002069-22 | Sponsor Protocol Number: ET17-057 | Start Date*: 2018-04-18 | |||||||||||
Sponsor Name:CENTRE LEON BERARD | |||||||||||||
Full Title: BREASTIMMUNE02 - A multicenter, randomized, open-label, Phase II trial aiming to evaluate the impact of pegfilgrastim on trastuzumab anti-tumor effect and antibody-dependent cell-mediated cytotoxic... | |||||||||||||
Medical condition: Operable HER2 positive breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011899-30 | Sponsor Protocol Number: 20080259 | Start Date*: 2009-12-18 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study of Pegfilgrastim Administered to Subjects With Newly Diagnosed, Locally-advanced or Metastatic Colorectal Cancer Treated With Bevacizum... | |||||||||||||
Medical condition: Locally-advanced or Metastatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) CZ (Completed) BE (Completed) IE (Completed) IT (Completed) FR (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006069-34 | Sponsor Protocol Number: 1564 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Clinical efficacy and cell mobilization activity of pegfilgrastim in patients with gynaecological malignancies in therapy with topotecan. | |||||||||||||
Medical condition: ovarian cancer, cervical cancer, endometrial cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001284-23 | Sponsor Protocol Number: XM22-ONC-305 | Start Date*: 2013-12-10 | |||||||||||
Sponsor Name:Merckle GmbH | |||||||||||||
Full Title: A randomized, phase IIIB, open-label, two-arm, multicenter, comparatiVe study on efficacy and safety of lipegfilgrastim (Lonquex, TEVA) in comparison to pegfilgrastim (Neulasta®, Amgen) in elderly ... | |||||||||||||
Medical condition: The study population includes patients with aggressive B cell Non-Hodgkin Lymphoma (NHL) planned to receive systemic anti-cancer therapy with at least 6 cycles of R-CHOP-21, according to local stan... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004792-14 | Sponsor Protocol Number: 0298-21 | Start Date*: 2021-09-08 | |||||||||||
Sponsor Name:Intas Pharmaceuticals Ltd. | |||||||||||||
Full Title: A Randomized, Active-Controlled, Multicenter, Open label, Two Arm Study to Assess Safety, Efficacy, Pharmacodynamics, and Pharmacokinetics with Pegfilgrastim PFS of Intas Pharmaceutical Limited Com... | |||||||||||||
Medical condition: Paediatric Patients Under 6 years of Age with Rhabdomyosarcoma or Wilms’ Tumour on Myelosuppressive Chemotherapy (CmT) Regimen | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002693-20 | Sponsor Protocol Number: GX‐G3_NHL_2/CGX14001 | Start Date*: 2016-01-21 | |||||||||||
Sponsor Name:Ilkogen Ilac San. ve Tic. A.S. | |||||||||||||
Full Title: A randomized, parallel group, multi-centre phase-2 study of GX-G3 compared with pegfilgrastim as an adjunct to chemotherapy in patients with Non-Hodgkin’s Lymphoma | |||||||||||||
Medical condition: Neutropenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001963-52 | Sponsor Protocol Number: GAMEC II | Start Date*: 2006-07-03 |
Sponsor Name:Queen Mary University London | ||
Full Title: GAMEC-SHORT (S) & GAMEC-ANTHRACYCLINE (A) RISK-ADAPTED PROTOCOL FOR RELAPSED GERM CELL TUMOURS (GCT) | ||
Medical condition: Open-labelled, non-randomised clinical trial in patients with relapsed germ cell tumours (GCT.) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-002971-42 | Sponsor Protocol Number: PEG-HSR | Start Date*: 2006-06-19 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Outpatients high-dose chemotherapy supported by autologus peripheral blood stem and single-dose pegfilgrastim in patients with lymphoproliferative malignances. | |||||||||||||
Medical condition: patients affected by linphoproliferative pathologies | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006541-14 | Sponsor Protocol Number: ema3_pegAML | Start Date*: 2007-07-27 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: A phase II pilot trial to evaluate the efficacy of treatment with Pegilate G-CSF in a group of elderly patients AML without chemotherapy indications | |||||||||||||
Medical condition: acute mieloid leukemia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000103-29 | Sponsor Protocol Number: MM-PEG-08 | Start Date*: 2008-02-21 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: A single arm phase 2 study on the efficacy of Pegfilgrastim (Neulasta) after DCEP chemotherapy: a feasibility study in multiple myeloma patients eligible for autologous transplant. | |||||||||||||
Medical condition: multiple myeloma | |||||||||||||
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Population Age: Adults, 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: 2012-002039-28 | Sponsor Protocol Number: LA-EP06-302 | Start Date*: 2012-09-14 |
Sponsor Name:Sandoz GmbH | ||
Full Title: Pivotal study in breast cancer patients investigating efficacy and safety of LA-EP2006 and Neulasta® | ||
Medical condition: Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015999-10 | Sponsor Protocol Number: XM22-03 | Start Date*: 2010-03-02 | |||||||||||||||||||||
Sponsor Name:BioGeneriX AG | |||||||||||||||||||||||
Full Title: Efficacy and Safety of XM22 compared to pegfilgrastim in patients with breast cancer receiving chemotherapy. A multinational, multicentre, randomised, double-blind controlled study | |||||||||||||||||||||||
Medical condition: Breast cancer high risk stage II, III or IV according to AJCC classification | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004539-18 | Sponsor Protocol Number: PGCN-001 | Start Date*: 2018-08-27 | |||||||||||
Sponsor Name:Prolong Pharmaceuticals, LLC | |||||||||||||
Full Title: A Phase 2, Open-Label, Multicenter, Efficacy, Safety, Tolerability, and Pharmacokinetic Study of ANF–Rho™ in Patients with Chronic Neutropenia | |||||||||||||
Medical condition: Chronic neutropenia | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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