Ultime prove


EudraCT Number: 2008-004583-40 Sponsor Protocol Number: 101010 Start Date:
Sponsor Name: Universitaetsklinikum Muenster
Full Title: A randomized, multi-center phase II trial to assess the efficay of 5-azacytidine added to standard primery therapy in elderly patients with newly diagnosed AML.
Medical condition: The disease under investigation is newly diagnosed Acute Myeloid Leucemia (AML) in elderly patients.
Disease: Version SOC Term Classification Code Term Level
13.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10000880 Acute myeloid leukaemia PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: View results

EudraCT Number: 2020-002936-55 Sponsor Protocol Number: MSC-EB_2020 Start Date:
Sponsor Name: Masarykova univerzita
Full Title: Safety and Efficacy of Allogenic Adipose Tissue-derived Mesenchymal Stromal Cells in Patients with Epidermolysis Bullosa: Clinical Trial Phase I/II
Medical condition: Epidermolysis bullosa congenita
Disease: Version SOC Term Classification Code Term Level
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults Gender: Male, Female
Trial protocol: CZ (Ongoing)
Trial results: (No results available)
EudraCT Number: 2021-002482-17 Sponsor Protocol Number: TAK-935-3003 Start Date:
Sponsor Name: Takeda Development Center Americas, Inc
Full Title: A Phase 3, Prospective, Open-Label, Multisite, Extension of Phase 3 Studies To Assess the Long-Term Safety and Tolerability of Soticlestat as Adjunctive Therapy in Subjects With Dravet Syndrome or ...
Medical condition: Dravet Syndrome (DS) Lennox-Gastaut Syndrome (LGS)
Disease: Version SOC Term Classification Code Term Level
20.0 100000004850 10073682 Dravet syndrome LLT
20.1 10029205 - Nervous system disorders 10048816 Lennox-Gastaut syndrome PT
Population Age: Children, Adolescents, Under 18, Adults Gender: Male, Female
Trial protocol: BE (Ongoing) ES (Ongoing) NL (Ongoing) HU (Ongoing) FR (Ongoing) GR (Ongoing) IT (Ongoing) LV (Ongoing) PL (Ongoing) Outside EU/EEA
Trial results: (No results available)

EudraCT Number: 2012-002328-34 Sponsor Protocol Number: KB056 Start Date:
Sponsor Name: KEDRION S.P.A
Full Title: Efficacy and safety evaluation of Kedrion Fibrin Sealant as an adjuvant for the control of hemostasis in pediatric patients undergoing abdominal or orthopedic surgery. Multicenter, randomized, cont...
Medical condition: Paediatric patients undergoing abdominal or orthopedic surgery
Disease: Version SOC Term Classification Code Term Level
18.0 10042613 - Surgical and medical procedures 10067439 Haemostasis PT
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 Gender: Male, Female
Trial protocol: IT (Prematurely Ended)
Trial results: (No results available)
EudraCT Number: 2015-003019-39 Sponsor Protocol Number: Start Date:
Sponsor Name:
Full Title: Efficacy & Safety of Nasal Influenza Immunisation in Children - The SNIFFLE-3 study
Medical condition: Children aged 2-18 years (inclusive), some of whom will have asthma and/or food allergies.
Disease: Version SOC Term Classification Code Term Level
18.0 100000004870 10001738 Allergy LLT
Population Age: Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: View results

EudraCT Number: 2020-000976-40 Sponsor Protocol Number: ION373-CS1 Start Date:
Sponsor Name: Ionis Pharmaceuticals, Inc
Full Title: A Phase 1-3, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ION373 in Patients with Alexand...
Medical condition: Alexander Disease
Disease: Version SOC Term Classification Code Term Level
22.1 10010331 - Congenital, familial and genetic disorders 10083059 Alexander disease PT
Population Age: Children, Adolescents, Under 18, Adults Gender: Male, Female
Trial protocol: GB (GB - no longer in EU/EEA) NL (Ongoing) IT (Ongoing)
Trial results: (No results available)
EudraCT Number: 2009-017477-38 Sponsor Protocol Number: MEK112110 Start Date:
Sponsor Name: GlaxoSmithKline Research & Development Ltd
Full Title: An Open-Label, Dose-Escalation, Phase IB/ II Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of the MEK Inhibitor GSK1120212 in Combination with Oral Evero...
Medical condition: Solid Tumors
Disease: Version SOC Term Classification Code Term Level
12.1 10059515 Non-small cell lung cancer metastatic LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed) ES (Prematurely Ended)
Trial results: View results

EudraCT Number: 2009-009320-36 Sponsor Protocol Number: 28431754DIA3009 Start Date:
Sponsor Name: Janssen Cilag International NV
Full Title: A Randomized, Double-Blind, 3-Arm Parallel-Group, 2-Year (104-Week), Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ 28431754 100 mg and JNJ-28431754 300 mg Compared Wit...
Medical condition: Type 2 Diabetes Mellitus
Disease: Version SOC Term Classification Code Term Level
9.1 10045242 Type II diabetes mellitus LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: NO (Completed) DE (Completed) FI (Completed) SK (Completed) DK (Completed) BG (Completed)
Trial results: View results
EudraCT Number: 2009-015125-36 Sponsor Protocol Number: NCT00934687 Start Date:
Sponsor Name: Medical School Hannover. Department of Psychiatry, Social Psychiatry and Psychotherapy
Full Title: Clostridium botulinum Typ A Neurotoxinkomplex zur adjuvanten Behandlung von depressiven Störungen – Eine randomisierte, kontrollierte Pilotstudie
Medical condition: Botulinum Toxin for the Treatment of Depression
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: (No results available)

EudraCT Number: 2006-000846-38 Sponsor Protocol Number: R076477-BIM-3004 Start Date:
Sponsor Name: Janssen-Cilag International N.V.
Full Title: A Randomized, Double-Blind, Active- and Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of Extended-Release Paliperidone as Maintenance Treatment After an ...
Medical condition: Bipolar I disorder, most recent maniac or mixed episode
Disease: Version SOC Term Classification Code Term Level
9.0 10004939 LLT
Population Age: Adults Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: View results
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