- ICH GCP
- EU: n kliinisten tutkimusten rekisteri
Viimeisimmät kokeilut
EudraCT Number: 2021-000214-42 | Sponsor Protocol Number: 755-201-EB | Start Date: | |||||||||||
Sponsor Name: InMed Pharmaceuticals Inc. | |||||||||||||
Full Title: A Randomised, Double-Blind, Vehicle-Controlled Phase 2 Study of Topically Applied INM-755 (cannabinol) Cream in Patients with Epidermolysis Bullosa. | |||||||||||||
Medical condition: Epidermolysis bullosa | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) AT (Completed) GR (Ongoing) IT (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001624-14 | Sponsor Protocol Number: LE3301 | Start Date: | |||||||||||
Sponsor Name: Pharming Technologies B.V. | |||||||||||||
Full Title: An Open-Label, Single Arm Study of the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of Leniolisib in Pediatric Patients (Aged 4 to 11 Years) With APDS (Activated Phosphoinositide 3-Kina... | |||||||||||||
Medical condition: Activated Phosphoinositide 3-Kinase Delta Syndrome | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004988-30 | Sponsor Protocol Number: 23386753 | Start Date: | ||||||
Sponsor Name: Mater Misercordiae Hospital - Department of Anaesthesia | ||||||||
Full Title: PHARMACOKINETICS AND ANALGESIC EFFICACY OF LAEVOBUPIVACAINE, FENTANYL AND CLONIDINE FOR POSTOPERATIVE PARAVERTEBRAL ANAESTHESIA. | ||||||||
Medical condition: We are aiming to provide postoperative analgesia for breast surgery | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: IE (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017347-33 | Sponsor Protocol Number: Clofarabine | Start Date: | ||||||||||||||||
Sponsor Name: University of Leipzig | ||||||||||||||||||
Full Title: A multicenter Phase I/II trial investigating the safety and efficacy (CR rate and OS) of low dose AraC with Clofarabine in patients ≥60 years with AML not eligible for conventional Chemotherapy | ||||||||||||||||||
Medical condition: Acute myeloid leukaemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002652-14 | Sponsor Protocol Number: 701003.01.010 | Start Date: | |||||||||||
Sponsor Name: Dr. Willmar Schwabe GmbH & Co. KG | |||||||||||||
Full Title: Safety and tolerability of Pelargonium sidoides extract EPs®7630 in children (1 to 5 years old) suffering from acute bronchitis | |||||||||||||
Medical condition: Acute bronchitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017319-13 | Sponsor Protocol Number: C-09-033 | Start Date: | |||||||||||
Sponsor Name: Alcon Research Ltd. | |||||||||||||
Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Media with Otorrhea in Tympanostomy Tubes | |||||||||||||
Medical condition: Acute otitis media with otorrhea in tympanostomy tubes | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) BE (Completed) FI (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001560-37 | Sponsor Protocol Number: GEM-658-EBE-0024-I | Start Date: | |||||||||||
Sponsor Name: Medizinische Fakultät der TU-München, vertreten durch den Dekan | |||||||||||||
Full Title: Sequentielle Kombination einer Chemotherapie mit Gemcitabine/Oxaliplatin und photodynamischen Therapie beim fortgeschrittenen Gallengangskarzinom | |||||||||||||
Medical condition: - advanced cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005391-29 | Sponsor Protocol Number: 2021/2014 | Start Date: | ||||||
Sponsor Name: Medical University of Vienna | ||||||||
Full Title: Effects of mannitol on delayed graft function after cadaveric renal transplantation | ||||||||
Medical condition: Kidney transplantation | ||||||||
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Population Age: | Gender: Male, Female | |||||||
Trial protocol: AT (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005197-78 | Sponsor Protocol Number: 1 | Start Date: | |||||||||||
Sponsor Name: Queen's Medical Centre, Nottingham, University Hospital NHS Trust, | |||||||||||||
Full Title: A multi-centre, randomised, parallel group, cross-over study comparing the efficacy and safety of double versus multiple injections of Botulinum Toxin type-A (Dysport®), into the gastrocnemius musc... | |||||||||||||
Medical condition: Spasticity of the Gastrocnemius Muscle due to Cerebral Palsy | |||||||||||||
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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: 2018-003281-14 | Sponsor Protocol Number: FCR173011/ResToP | Start Date: | |||||||||||
Sponsor Name: Fundación CRIS contra el Cáncer | |||||||||||||
Full Title: Multicenter, Open-Label, Single Arm, Phase II Exploratory Study to Evaluate the Reinduction and second stop of TKI with Ponatinib in CML in Molecular Response (ResToP) | |||||||||||||
Medical condition: Chronic myelogenous leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |