- Trials with a EudraCT protocol (69)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
69 result(s) found for: Interferon alfa-2b.
Displaying page 2 of 4.
EudraCT Number: 2008-007649-30 | Sponsor Protocol Number: BLX883-203 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:Biolex Therapeutics Inc. | |||||||||||||
Full Title: SELECT-2: Phase 2B, Partially Blinded, Randomized Study In Treatment Naïve Subjects With HCV Genotype 1 To Compare The Efficacy, Safety, And Tolerability Of Three Doses of Locteron™ Plus Ribavirin ... | |||||||||||||
Medical condition: Approximately 100 treatment-naïve adults with chronic hepatitis C genotype 1, who meet eligibility criteria, will be enrolled at approximately 35 study sites in Europe and the United States (U.S.). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BG (Completed) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001260-36 | Sponsor Protocol Number: MEN-TOS | Start Date*: 2008-03-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Terapia PEG-Interferone alfa 2B+Ribavirina versus terapia PEG-Interferone alfa 2B + Ribavirina+ Terapia ormonale sostitutiva (TOS) nella prevenzione della progressione della fibrosi epatica nell’ep... | |||||||||||||
Medical condition: Women in post-menopause with Chronic HCV positive hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003409-18 | Sponsor Protocol Number: RRC-2/3-2006 | Start Date*: 2006-11-20 |
Sponsor Name:Sahlgrenska University Hospital, Östra | ||
Full Title: An Open-label, Multicenter Study Evaluating the Efficacy and Safety of 24 or 48 weeks pegylated interferon alfa-2a 40 kD (PEGASYS®) Combination Therapy with Ribavirin (Copegus®) in Patients with Ch... | ||
Medical condition: chronic hepatitis C (CHC) virus infection genotype 2 or 3 who responded during (i.e. had HCV-RNA < 50 IU/mL at the end of previous therapy), but relapsed after (i.e. had detectable HCV-RNA after th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) DK (Completed) FI (Completed) | ||
Trial results: (No results available) |
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: 2007-005151-42 | Sponsor Protocol Number: P05101 | Start Date*: 2008-08-28 | ||||||||||||||||||||||||||
Sponsor Name:Schering Plough Research Institute, A Division of Schering Corporation | ||||||||||||||||||||||||||||
Full Title: A Phase 3 Safety and Efficacy Study of Boceprevir in Subjects With Chronic Hepatitis C Genotype 1 Who Failed Prior Treatment With Peginterferon/Ribavirin | ||||||||||||||||||||||||||||
Medical condition: Chronic Hepatitis C | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) PT (Prematurely Ended) ES (Completed) IT (Completed) BE (Completed) DE (Completed) GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012010-52 | Sponsor Protocol Number: mRCC | Start Date*: 2009-08-04 | |||||||||||
Sponsor Name:Department of Oncology, Aarhus University Hospital | |||||||||||||
Full Title: Bevacizumab, Interleukin-2 and Interferon-alpha in metastathic renal cell carcinoma | |||||||||||||
Medical condition: Patient with previously untreated Metastatic Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006803-35 | Sponsor Protocol Number: CABF656A2201 | Start Date*: 2008-02-21 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An open-label, randomized, multicenter, active-controlled, dose-ranging study to evaluate the safety and efficacy of albinterferon alfa-2b administered every 4 weeks plus ribavirin in interferon al... | |||||||||||||
Medical condition: CHONIC HEPATITIS C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001044-44 | Sponsor Protocol Number: VX-950-TiDP24-C208 | Start Date*: 2007-08-01 | |||||||||||
Sponsor Name:Tibotec BVBA | |||||||||||||
Full Title: A Phase IIa randomized, open-label study of telaprevir (VX-950) administered every 12 or every 8 hours in combination with either Peg-IFN alfa2a (Pegasys®) and ribavirin (Copegus®) or Peg-IFN alfa2... | |||||||||||||
Medical condition: Hepatitis C infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011182-86 | Sponsor Protocol Number: BLX883-204 | Start Date*: 2009-07-24 | |||||||||||
Sponsor Name:Biolex Therapeutics, Inc | |||||||||||||
Full Title: 480 Study: Phase 2b Open-label, Randomized Study in Treatment Naïve Subjects with HCV Genotype 1 to Compare the Efficacy, Safety, and Tolerability of the 480 µg Dose of Locteron™ Plus Ribavirin ... | |||||||||||||
Medical condition: Approximately 72 subjects with chronic hepatitis C (treatment naive, genotype 1) will be included in a 12 week open label randomized trial with 2 panels (approximately 40 subjects in PANEL A and ap... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2011-002911-27 | Sponsor Protocol Number: BOC-PR | Start Date*: 2011-09-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PARMA | |||||||||||||
Full Title: Effect of boceprevir therapy on HCV-specific T cell responses: perspectives of immune monitoring and immune therapy | |||||||||||||
Medical condition: Chronic active hepatitis C never treated previously with anti-viral terapie | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023124-24 | Sponsor Protocol Number: LUMCCHIP | Start Date*: 2011-03-02 | |||||||||||
Sponsor Name:Academisch Ziekenhuis Leiden acting under the name of Leids Universitair Medisch Centrum | |||||||||||||
Full Title: Chemo-Immunotherapy, gemcitabine with pegylated interferon alpha-2b (Peg-Intron) with and without p53 synthetic long peptide (p53 SLP) vaccine, for patients with platinum resistant ovarian cancer. ... | |||||||||||||
Medical condition: Recurrent platinum resistant, p53 positive ovarian cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003538-11 | Sponsor Protocol Number: 1220.5 | Start Date*: 2008-10-01 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: Antiviral effect, safety and pharmacokinetics of BI 201335 NA in hepatitis C virus genotype 1 infected treatment-naïve and treatment-experienced patients for 24 weeks as combination therapy with pe... | |||||||||||||
Medical condition: chronic hepatitis C infection of genotype 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Completed) NL (Completed) PT (Completed) GB (Completed) AT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004257-29 | Sponsor Protocol Number: 11-12 | Start Date*: 2013-05-03 | |||||||||||
Sponsor Name: All Ireland Cooperative Oncology Research Group ( ICORG) | |||||||||||||
Full Title: A Phase III Randomized Study of Adjuvant Ipilimumab Anti-CTLA4 Therapy Versus High-Dose Interferon α-2b for Resected High-Risk Melanoma | |||||||||||||
Medical condition: High-risk resected melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001264-31 | Sponsor Protocol Number: P03659 | Start Date*: 2005-07-06 | |||||||||||
Sponsor Name:SCHERING-PLOUGH | |||||||||||||
Full Title: Peg-Intron/Rebetol vs Peg-Intron / SCH 503034 with and without Ribavirin in Chronic Hepatitis C HCV 1 Peginterferon alfa/Ribavirin Nonresponders: A SCH 503034 dose finding Phase 2 Study. | |||||||||||||
Medical condition: Adult patients with Chronic hepatitis C HCV-1 without cirrhosis nonresponders to a previous standard treatment of 12 weeks. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004717-25 | Sponsor Protocol Number: Low-PV | Start Date*: 2016-07-08 | |||||||||||
Sponsor Name:FONDAZIONE PER LA RICERCA OSPEDALE MAGGIORE DI BERGAMO - FROM | |||||||||||||
Full Title: The benefit/risk profile of pegylated proline-Interferon alpha-2b (AOP2014) added to the best available strategy based on phlebotomies in low-risk patients with Polycythemia Vera (PV). The Low-PV r... | |||||||||||||
Medical condition: Polycythemia Vera | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003295-12 | Sponsor Protocol Number: 15022013 | Start Date*: 2013-10-31 | |||||||||||||||||||||
Sponsor Name:Roskilde University Hospital | |||||||||||||||||||||||
Full Title: Combination Therapy Interferon Alpha + JAK1-2 Inhibitor in The Ph-Negative Chronic Myeloid Neoplasms | |||||||||||||||||||||||
Medical condition: | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024557-36 | Sponsor Protocol Number: VHCRP1007 | Start Date*: 2012-05-29 | |||||||||||
Sponsor Name:The Kirby Institute | |||||||||||||
Full Title: A phase IV open-label multicentre, international trial of response guided treatment with directly observed pegylated interferon alfa 2b and self-administered ribavirin for patients with chronic HCV... | |||||||||||||
Medical condition: Chronic Hepatitis C genotype 2 and 3 infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005161-11 | Sponsor Protocol Number: 116/2005U/Sper | Start Date*: 2005-08-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Treatment with leucocytic interferon-alpha more ribavirine towards peg-interferon to reduced doses more ribavirine in patients affections from positive chronic hepatitis HCV that in course of arran... | |||||||||||||
Medical condition: CHRONIC HEPATITIS FROM VIRUS C | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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