- Trials with a EudraCT protocol (2,069)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,069 result(s) found for: Drug testing.
Displaying page 2 of 104.
EudraCT Number: 2020-001288-99 | Sponsor Protocol Number: C4221015 | Start Date*: 2020-11-26 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: AN OPEN-LABEL, MULTICENTER, RANDOMIZED PHASE 3 STUDY OF FIRST LINE ENCORAFENIB PLUS CETUXIMAB WITH OR WITHOUT CHEMOTHERAPY VERSUS STANDARD OF CARE THERAPY WITH A SAFETY LEAD-IN OF ENCORAFENIB AND C... | |||||||||||||
Medical condition: Colorectal cancer (BRAF V600E-mutant mCRC) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) GB (GB - no longer in EU/EEA) NL (Ongoing) DE (Ongoing) FR (Not Authorised) BE (Trial now transitioned) SE (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) SK (Trial now transitioned) BG (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002661-21 | Sponsor Protocol Number: CLAF237A2323 | Start Date*: 2005-02-28 |
Sponsor Name:Novartis Farmaceutica S. A. | ||
Full Title: A multicenter, randomized, double-blind active controlled study to compare the effect of 24 weeks treatment with LAF237 50 mg bid to acarbose up to 100 mg tid in drug naïve patients with type 2 dia... | ||
Medical condition: Type II Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001088-28 | Sponsor Protocol Number: BRIO | Start Date*: 2016-01-14 | ||||||||||||||||
Sponsor Name:South London and Maudsley NHS Foundation Trust [...] | ||||||||||||||||||
Full Title: Feasibility, efficacy and acceptability of injected buprenorphine as treatment for opiate users who persist in injecting illicit heroin through opiate maintenance treatment | ||||||||||||||||||
Medical condition: Addiction to illicit heroin | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000625-30 | Sponsor Protocol Number: INOT22 | Start Date*: 2004-07-21 |
Sponsor Name:INO Therapeutics | ||
Full Title: Comparison of Supplemental Oxygen and Nitric Oxide for Inhalation Plus Oxygen in the Evaluation of the Reactivity of the Pulmonary Vasculature During Acute Pulmonary Vasodilator Testing | ||
Medical condition: : Nitric Oxide for inhalation at 800ppm, plus 100% O2, to be used to assess pulmonary vaso reactivity during Pulmonary Vasodilator Testing | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000709-26 | Sponsor Protocol Number: 50510617 | Start Date*: 2022-01-18 | |||||||||||
Sponsor Name:Rigshospitalet, Centre of Head and Orthopaedics | |||||||||||||
Full Title: Drug test detection 24 hours after nasal administration of cocaine as a local vasoconstrictor prior to nasal intubation | |||||||||||||
Medical condition: Residual systemic cocaine after administration as local nasal vasoconstrictor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000540-24 | Sponsor Protocol Number: CLAF237A2310 | Start Date*: 2004-12-15 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multicenter, double-blind, randomized, active controlled study to compare the effect of long term treatment with LAF237 50 mg bid to gliclazide up to 320 mg daily in drug naïve patients with type... | ||
Medical condition: Type II Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) IE (Completed) GB (Completed) DE (Completed) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002111-41 | Sponsor Protocol Number: AI438-047 | Start Date*: 2015-05-06 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Multi-arm Phase 3 Randomized Placebo Controlled Double Blind Clinical Trial to Investigate the Efficacy and Safety of BMS-663068 in Heavily Treatment Experienced Subjects Infected with Multi-drug... | |||||||||||||
Medical condition: HIV, Adult | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Completed) BE (Completed) NL (Ongoing) GB (Completed) NO (Prematurely Ended) IE (Completed) PT (Completed) GR (Completed) FR (Completed) RO (Trial now transitioned) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011445-13 | Sponsor Protocol Number: IJB-BGDO-2009-001 | Start Date*: 2009-11-26 |
Sponsor Name:Institut Jules Bordet-Université Libre de Bruxelles | ||
Full Title: Preoperative chemosensitivity testing as Predictor of Treatment benefit in Adjuvant stage III colon cancer | ||
Medical condition: Stage III colon adenocarcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003881-32 | Sponsor Protocol Number: 023-01 | Start Date*: 2007-09-20 | |||||||||||
Sponsor Name:Merck & Co, Inc | |||||||||||||
Full Title: Early Access of MK-0518 in Combination With an Optimized Background Antiretroviral Therapy (OBT) in Highly Treatment Experienced HIV-1 Infected Patients With Limited to No Treatment Options. | |||||||||||||
Medical condition: HIV-1 infected patients | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Completed) ES (Completed) DE (Completed) SE (Prematurely Ended) AT (Completed) NL (Completed) LV (Completed) IT (Completed) EE (Completed) SI (Completed) IE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004889-18 | Sponsor Protocol Number: 1.3 | Start Date*: 2022-04-21 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effect of Dupilumab in patients with aspirin-exacerbated respiratory disease (AERD) -A single-center prospective pilot study | ||
Medical condition: Aspirin-exacerbated respiratory disease (AERD), also known as Samter's Triad or Widal's triad, comprises the triad of allergic asthma, chronic rhinosinusitis with nasal polyps (CRswNP) and nonstero... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003409-25 | Sponsor Protocol Number: S61887 | Start Date*: 2018-11-08 |
Sponsor Name:KU Leuven | ||
Full Title: Dose-dependent effects of propranolol on extinction learning and return of fear | ||
Medical condition: Experimental study with healthy participants recruited from the general population; no vulnerable individuals or clinical groups will be involved. Our objective is to test whether propranolol admin... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002714-11 | Sponsor Protocol Number: EORTC 22033-26033 | Start Date*: 2005-06-06 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Primary chemotherapy with temozolomide vs. radiotherapy in patients with low grade gliomas after stratification for genetic 1p loss: a phase III study | |||||||||||||
Medical condition: Histologically proven low-grade glioma ♦ Astrocytoma WHO grade II (gemistocytic, fibrillary and protoplasmatic) ♦ Oligoastrocytoma WHO grade II ♦ Oligodendroglioma WHO grade II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) GB (Completed) IT (Completed) DK (Prematurely Ended) BE (Completed) ES (Completed) PT (Completed) HU (Completed) SE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001636-22 | Sponsor Protocol Number: TROPICALACS | Start Date*: 2013-08-26 | |||||||||||
Sponsor Name:Hospital of the University of Munich, Grosshadern | |||||||||||||
Full Title: A prospective, randomized, parallel-group, open label, non-inferiority, multicenter trial of a 12 month vs. a short-term platelet function testing guided prasugrel therapy in acute coronary syndrom... | |||||||||||||
Medical condition: Troponin positive acute coronary syndrome after successful percutaneous coronary intervention with an indication for a standard treatment of 12 month with prasugrel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) AT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003611-62 | Sponsor Protocol Number: LIB003-003 | Start Date*: 2020-03-20 | |||||||||||
Sponsor Name:LIB Therapeutics, LLC | |||||||||||||
Full Title: Randomized, Open-Label, Cross-Over, Phase 3 Study to Evaluate the Efficacy and Safety of LIB003 with Evolocumab in Homozygous Familial Hypercholesterolemia Patients on Stable Lipid-Lowering Therapy. | |||||||||||||
Medical condition: Homozygous Familial Hypercholesterolemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003325-41 | Sponsor Protocol Number: 668353 | Start Date*: 2017-06-09 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: PREemptive Pharmacogenomic testing for Preventing Adverse drug REactions | ||
Medical condition: Adverse drug reactions | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004011-20 | Sponsor Protocol Number: GS-US-380-1878 | Start Date*: 2016-02-12 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Switching from Regimens Consisting of Boosted Atazanavir or Darunavir plus either Emtricitabine/Tenofovir or Abacavir/... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV-1) Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004500-40 | Sponsor Protocol Number: CC-5013-NHL-003 | Start Date*: 2007-03-28 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE II, MULTICENTER, SINGLE-ARM, OPEN-LABEL STUDY TO EVALUATE THE SAFETY AND EFFICACY OF SINGLE-AGENT LENALIDOMIDE (REVLIMID®) IN SUBJECTS WITH RELAPSED OR REFRACTORY AGGRESSIVE NON-HODGKIN’S L... | |||||||||||||
Medical condition: Relapsed or refractory aggressive non-Hodgkin's lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004838-41 | Sponsor Protocol Number: CSOK583A12301 | Start Date*: 2021-03-04 | |||||||||||
Sponsor Name:Hexal AG | |||||||||||||
Full Title: A 52-week multicenter, randomized, double-masked, 2-arm parallel study to compare efficacy, safety and immunogenicity of SOK583A1 to Eylea®, administered intravitreally, in patients with neovascula... | |||||||||||||
Medical condition: The ‘wet’ form of age-related macular degeneration (AMD) is a disease which affects the central part of the retina (called the macula) at the back of the eye. The wet form of AMD is caused by choro... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) LV (Completed) FR (Completed) SK (Completed) BG (Completed) HU (Completed) PT (Completed) AT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002940-82 | Sponsor Protocol Number: CLAF237A2355 | Start Date*: 2004-12-16 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multicenter, randomized, double-blind, active controlled study to compare the effect of 24 weeks treatment with combination therapy of LAF237 and pioglitazone to LAF237 monotherapy or pioglitazon... | ||
Medical condition: Type II Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) CZ (Completed) GB (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002794-51 | Sponsor Protocol Number: CLMF237A2302 including amd 2 | Start Date*: 2006-09-20 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, active-controlled, multicentre study to compare the effect of 24 weeks treatment with a fixed combination therapy of vildagliptin and metformin to the individual monothe... | ||
Medical condition: Type II Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) SE (Completed) IT (Completed) HU (Completed) | ||
Trial results: View results |
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