Últimos ensayos


EudraCT Number: 2014-004897-40 Sponsor Protocol Number: GABA-2 Start Date:
Sponsor Name: PHARM – Pharmaceutical Research Management srl
Full Title: Randomized, double-blind, placebo controlled, multi-centre, superiority phase II study to evaluate the safety, pharmacokinetic, efficacy of gabapentin liquid formulation as add-on to morphine in ch...
Medical condition: Chronic pain of neuropathic or mixed origin
Disease: Version SOC Term Classification Code Term Level
19.1 100000004852 10054095 Neuropathic pain LLT
Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: DE (Prematurely Ended) FR (Ongoing) NL (Prematurely Ended) IT (Prematurely Ended)
Trial results: (No results available)

EudraCT Number: 2021-002339-44 Sponsor Protocol Number: IGM-2323-001 Start Date:
Sponsor Name: IGM Biosciences, Inc.
Full Title: A Phase 1/2 Open-Label, Multicenter Study Evaluating the Safety and Pharmacokinetics of Escalating Doses of IGM-2323 in Subjects with Relapsed/Refractory Non-Hodgkin Lymphomas
Medical condition: Relapsed/Refractory (R/R) Non-Hodgkin lymphomas (NHL)
Disease: Version SOC Term Classification Code Term Level
23.0 100000004864 10025311 Lymphoma (non-Hodgkin's) LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: CZ (Completed) ES (Ongoing) IT (Ongoing) DK (Prematurely Ended)
Trial results: (No results available)
EudraCT Number: 2010-018781-23 Sponsor Protocol Number: 2917800009 Start Date:
Sponsor Name: Top Institute Food and Nutrition
Full Title: Diagnose of GH-deficiency: comparing the dietary-protein test with conventional Growth Hormone Stimulation Tests
Medical condition: To investigate if there is a correlation between the peak GH concentrations after ingestion of gelatin protein and the peak GH concentrations after the two standard tests (GHST) in order to discrim...
Disease: Version SOC Term Classification Code Term Level
12.1 10056438 Growth hormone deficiency LLT
Population Age: Children, Under 18 Gender: Male, Female
Trial protocol: NL (Ongoing)
Trial results: (No results available)

EudraCT Number: 2015-003509-41 Sponsor Protocol Number: GBG90 Start Date:
Sponsor Name: GBG Forschungs GmbH
Full Title: A randomized phase II trial to assess the efficacy of paclitaxel and olaparib in comparison to paclitaxel / carboplatin followed by epirubicin/cyclophosphamide as neoadjuvant chemotherapy in patien...
Medical condition: Patients with triple negative or HRpositive, early breast cancer
Disease: Version SOC Term Classification Code Term Level
20.0 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10006187 Breast cancer PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: (No results available)
EudraCT Number: 2015-002882-41 Sponsor Protocol Number: AIBDSG_002 Start Date:
Sponsor Name: Medical University of Vienna (MUW)
Full Title: Sono-­Response-­Study A Pilot Study on the use of contrast enhanced ultrasound in Crohn’s disease
Medical condition: Inflammatory bowel disease (Crohn's disease)
Disease: Version SOC Term Classification Code Term Level
18.1 10017947 - Gastrointestinal disorders 10011401 Crohn's disease PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: AT (Ongoing)
Trial results: (No results available)

EudraCT Number: 2010-024094-39 Sponsor Protocol Number: Adip-2010 Start Date:
Sponsor Name: University of Ulm, University Hospital Ulm
Full Title: Offene, monozentrische, nicht kontrollierte und nicht randomisierte Phase IV-Studie zur Bestimmung der Pharmakokinetik von Carbapenemen in adipösen Patienten.
Medical condition: The purpose of this study is to determine the free tissue kinetics of ertapenem and meropenem in fatty tissue and intraperitoneal fluid up to 24 hours after administration of the IMP. Subjects are ...
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: View results
EudraCT Number: 2005-003023-40 Sponsor Protocol Number: 21805 Start Date:
Sponsor Name: Food Standards Agency
Full Title: The role of peanut specific T cell responses in children with peanut allergy and in children who are tolerant to peanuts
Medical condition: Children with Peanut Allergy
Disease: Version SOC Term Classification Code Term Level
Population Age: Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: GB (GB - no longer in EU/EEA)
Trial results: (No results available)

EudraCT Number: 2020-005019-29 Sponsor Protocol Number: Rux-cALL-Pol_2020 Start Date:
Sponsor Name: Medical University of Lodz
Full Title: Single-arm interventional study with ruxolitinib and AIOEP-BFM2017 chemotherapy in children with acute lymphoblastic leukemia and confirmed activation of JAK/STAT pathway.
Medical condition: Acute Lymphoblastic Leukemia with confirmed activating of JAK/STAT pathway in children and adolescents
Disease: Version SOC Term Classification Code Term Level
21.0 100000004864 10000845 Acute lymphoblastic leukemia LLT
22.0 100000004850 10072213 JAK-2 mutation LLT
Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: PL (Ongoing)
Trial results: (No results available)
EudraCT Number: 2007-000730-40 Sponsor Protocol Number: SOCRATES Start Date:
Sponsor Name: Heinrich-Heine-Universität Düsseldorf
Full Title: Phase II study evaluating transarterial chemoembolization (TACE) in combination with sorafenib for the treatment of advanced hepatocellular carcinoma (HCC)
Medical condition: histologically proven advanced hepatocellular carcinoma (HCC) not suitable for resection or liver transplantation but without extrahepatic manifestations and without previous treatment for HCC
Disease: Version SOC Term Classification Code Term Level
9.1 10019828 Hepatocellular carcinoma non-resectable LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Prematurely Ended)
Trial results: View results

EudraCT Number: 2009-011148-21 Sponsor Protocol Number: D0520C00012 Start Date:
Sponsor Name: AstraZeneca AB
Full Title: A 12-week, randomised, double-blind, placebo-controlled, parallel group, multinational, phase IIb dose range finding study to evaluate the efficacy and safety of AZD9668 administered orally at 3 do...
Medical condition: Chronic Obstructive Pulmonary Disease (COPD)
Disease: Version SOC Term Classification Code Term Level
9.1 10010952 COPD LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed) SK (Completed)
Trial results: View results
3
Suscribir