- Trials with a EudraCT protocol (179)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
179 result(s) found for: Pegylated interferon.
Displaying page 3 of 9.
EudraCT Number: 2004-002093-30 | Sponsor Protocol Number: NO17754 | Start Date*: 2005-12-22 |
Sponsor Name:F. Hoffmann-La Roche Ltd | ||
Full Title: Extension protocol for patients with Chronic Myelogenous Leukemia (CML), Malignant Melanoma (MM) or Renal Cell Carcinoma (RCC) that have responded to treatment with Pegylated-interferon α-2a (PEG-I... | ||
Medical condition: Treatment of CML, MM or RCC. | ||
Disease: | ||
Population Age: | Gender: | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021963-34 | Sponsor Protocol Number: 2125-202 | Start Date*: 2010-11-03 | |||||||||||
Sponsor Name:Idera Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Comparator-Controlled, 12-week Trial of IMO-2125 plus Ribavirin in Patients Infected with Hepatitis C Virus who were Nonresponders to Pegylated-Interferon plus ... | |||||||||||||
Medical condition: This is a Phase 2, randomized, double-blind, comparator-controlled study of IMO-2125 in hepatitis C-infected patients who were previously nonresponders to standard treatment (pegylated-interferon p... | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002703-13 | Sponsor Protocol Number: HGS1008-C1060 | Start Date*: 2007-03-20 | |||||||||||
Sponsor Name:Human Genome Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Multi-Center Study to Evaluate the Efficacy and Safety of Albumin Interferon Alfa-2b (alb-IFN) in Combination with Ribavirin Compared with Peginterferon Alfa-2a (PEGASYS or P... | |||||||||||||
Medical condition: Chronic hepatitis C (CHC) genotype 1. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) FR (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000523-40 | Sponsor Protocol Number: HAI115879 | Start Date*: 2012-09-11 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Devlopment Ltd | |||||||||||||
Full Title: A Phase II Multicenter, Parallel-Group, Randomized, Dose-Ranging Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Following 12 Weeks of Oral Administration of G... | |||||||||||||
Medical condition: Hepatitis C virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000773-71 | Sponsor Protocol Number: vem+IL-2v1.0 | Start Date*: 2013-07-12 | |||||||||||
Sponsor Name:Department of Oncology, Aarhus University Hospital | |||||||||||||
Full Title: A multicenter phase II study evaluating the efficacy and tolerability of vemurafenib in combination with Pegylated Interferon and Interleukin-2 in patients with BRAF-mutated metastatic melanoma | |||||||||||||
Medical condition: Metastatic melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002704-34 | Sponsor Protocol Number: HGS1008-C1067 | Start Date*: 2007-04-27 | |||||||||||
Sponsor Name:Human Genome Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Multi-Center Study to Evaluate the Efficacy and Safety of Albumin Interferon Alfa-2b (alb-IFN) in Combination with Ribavirin Compared with Peginterferon Alfa-2a (PEGASYS or P... | |||||||||||||
Medical condition: Chronic Hepatitis C (CHC) genotype 2/3. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) SE (Completed) GB (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003463-22 | Sponsor Protocol Number: AI452-030 | Start Date*: 2013-03-13 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: MAGNITUDE - A Phase 3 Evaluation of the Safety and Efficacy of Lambda/RBV/DCV in Treatment Naïve Subjects with Chronic HCV Infection, who have Underlying Mild or Moderate Hemophilia or Patients who... | |||||||||||||
Medical condition: Chronic Hepatitis C Virus Infection (Genotype 1b, 2, 3, 4) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Temporarily Halted) IT (Prematurely Ended) NL (Completed) FR (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004321-25 | Sponsor Protocol Number: NordDutchCML009 | Start Date*: 2013-04-03 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: A phase II, single arm, multicenter study of nilotinib in combination with pegylated interferon α2b in patients with suboptimal molecular response or stable detectable molecular residual disease af... | |||||||||||||
Medical condition: Chronic myeloid leukemia in chronic phase and ≥ 2 years on Imatinib treatment with suboptimal molecular response (BCR-ABL level above 0.01% IS). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) SE (Completed) NO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022067-35 | Sponsor Protocol Number: PP25213 | Start Date*: 2011-02-17 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: INFORM-SVR: A Randomized, Multi-Center Study of Interferon-Free Treatment with a Combination of a Polymerase Inhibitor (RO5024048) and a Ritonavir boosted HCV Protease Inhibitor (RO5190591/r, DNV/... | |||||||||||||
Medical condition: Chronic Hepatitis C (CHC) Genotype 1 (Arms A and B) and Genotypes 1b and 4 (Arm C) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002777-56 | Sponsor Protocol Number: ML28470 | Start Date*: 2012-08-20 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Cross-sectional multicenter study evaluating the IL28B polymorphism in patients with HBeAg-negative chronic hepatitis B treated with pegylated interferon alfa-2a in the course of Peg.Be.Liver study | |||||||||||||
Medical condition: HBeAg-negative chronic hepatitis B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004695-11 | Sponsor Protocol Number: AI452-020 | Start Date*: 2013-06-11 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3 Blinded Randomized Study of Peginterferon Lambda-1a and Ribavirin Compared to Peginterferon Alfa-2a and Ribavirin, Each Administered with Telaprevir in Subjects with Genotype-1 Chronic He... | |||||||||||||
Medical condition: Chronic Hepatitis C Virus (HCV) Infection (Genotype-1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) CZ (Completed) GB (Completed) PL (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000516-22 | Sponsor Protocol Number: 800MS301 | Start Date*: 2019-07-08 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, 3- Arm, Parallel-Group Study in Pediatric Subjects Aged 10 Through 17 Years to Evaluate the Efficacy and Safety of BG00012 and BIIB017 ... | ||||||||||||||||||
Medical condition: Relapsing Remitting Multiple Sclerosis (RRMS) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Not Authorised) EE (Prematurely Ended) HU (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024262-22 | Sponsor Protocol Number: CML-V | Start Date*: 2012-08-24 | |||||||||||
Sponsor Name:Friedrich-Schiller-Universität Jena | |||||||||||||
Full Title: Treatment optimization of newly diagnosed Ph/BCR-ABL positive patients with chronic myeloid leukemia (CML) in chronic phase with nilotinib vs. nilotinib plus interferon alpha induction and nilotini... | |||||||||||||
Medical condition: chronic phase CML | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002022-10 | Sponsor Protocol Number: NV21928 | Start Date*: 2008-09-23 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: Protocolo multicéntrico abierto en el que se proporciona interferón pegilado alfa-2a (PEGASYS®) en monoterapia o en combinación con ribavirina (COPEGUS®) a pacientes con hepatitis C crónica que han... | |||||||||||||
Medical condition: Chronic hepatitis C Hepatitis C crónica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Completed) FR (Completed) IT (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007075-16 | Sponsor Protocol Number: GE07-12 | Start Date*: 2008-12-01 | |||||||||||
Sponsor Name:VU university medical center | |||||||||||||
Full Title: The effect of peroxisome proliferator activator receptor γ agonist pre-treatment on pegylated interferon-α2a and ribavirin efficacy in hepatitis C patients, previously resistant to treatment with p... | |||||||||||||
Medical condition: Chronic hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001469-16 | Sponsor Protocol Number: TPL102357 | Start Date*: 2005-10-20 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: A double-blind, randomized, placebo-controlled, multi-centre, dose-ranging, parallel group, phase II study to assess efficacy, safety/tolerability, and pharmacokinetics of a thrombopoietin receptor... | ||
Medical condition: Thrombocytopenia caused by hepatitis-C | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001030-94 | Sponsor Protocol Number: KKS-227 | Start Date*: 2017-03-29 | |||||||||||
Sponsor Name:Philipps University Marburg | |||||||||||||
Full Title: Efficacy and safety of pegylated-proline-interferon alpha 2B (AOP2014) in maintaining deep molecular remissions in patients with chronic myeloid leukemia (CML) who discontinue ABL-kinase inhibitory... | |||||||||||||
Medical condition: Chronic myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005636-26 | Sponsor Protocol Number: HCV12-01 | Start Date*: 2012-04-13 |
Sponsor Name:Foundation for Liver Research | ||
Full Title: Effect of Telaprevir in triple therapy for chronic hepatitis C patients on Intrahepatic immunological Mechanisms | ||
Medical condition: Chronic hepatitis C | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002504-15 | Sponsor Protocol Number: NordCML002 | Start Date*: 2004-12-01 |
Sponsor Name:The Nordic CML Study Group | ||
Full Title: A RANDOMIZED PHASE II STUDY COMPARING IMATINIB AND THE COMBINATION OF IMATINIB AND PEGYLATED INTERFERON ALPHA-2B IN NEWLY DIAGNOSED NON-HIGH RISK CHRONIC MYELOID LEUKEMIA PATIENTS IN COMPLETE HEMAT... | ||
Medical condition: Newly diagnosed chronic myeloid leukemia (CML) belonging to intermedia (IR) or low risk (LR) by the Sokal prognostic score | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000533-22 | Sponsor Protocol Number: VX-950-TiDP24-C216 | Start Date*: 2008-11-14 | |||||||||||
Sponsor Name:Tibotec BVBA | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, Phase III trial of 2 regimens of telaprevir (with and without delayed start) combined with pegylated interferon alfa-2a (Pegasys®) and ribavirin (Cop... | |||||||||||||
Medical condition: Chronic genotype 1 Hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) SE (Completed) FR (Completed) AT (Completed) IT (Completed) GB (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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