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EudraCT Number: 2018-002611-99 Sponsor Protocol Number: 20090 Start Date:
Sponsor Name: Bayer AG
Full Title: Open-label, randomized, two–arm, controlled study to assess the efficacy, safety, and tolerability of intravitreal (IVT) aflibercept compared to laser photocoagulation in patients with retinopathy ...
Medical condition: Retinopathy of prematurity
Disease: Version SOC Term Classification Code Term Level
20.1 10015919 - Eye disorders 10038933 Retinopathy of prematurity PT
Population Age: Preterm newborn infants, Under 18 Gender: Male, Female
Trial protocol: CZ (Completed) SE (Completed) NL (Completed) PT (Completed) GB (GB - no longer in EU/EEA) BE (Completed) DE (Completed) SK (Completed) AT (Completed) BG (Completed) PL (Completed) ES (Completed) HU (Completed) LT (Completed) EE (Completed) LV (Completed) GR (Completed) IT (Completed) RO (Completed)
Trial results: View results

EudraCT Number: 2020-001240-25 Sponsor Protocol Number: MOURO48 Start Date:
Sponsor Name: Radboudumc
Full Title: Phase 2 INSPIRE trial: Ipilimumab with Nivolumab in molecular-selected patients with castration-resistant prostate cancer
Medical condition: (metastatic) castration-resistant prostate cancer
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male
Trial protocol: NL (Ongoing)
Trial results: (No results available)
EudraCT Number: 2012-005496-14 Sponsor Protocol Number: MRZ60201_3072_1 Start Date:
Sponsor Name: Merz Pharmaceuticals GmbH
Full Title: Prospective, multicenter, randomized, double-blind, parallel-group, dose-response study of three doses Xeomin® (incobotulinumtoxinA, NT 201) for the treatment of upper limb spasticity alone or comb...
Medical condition: Upper limb spasticity or combined upper and lower limb spasticity in children and adolescents (age 2 - 17 years) with cerebral palsy
Disease: Version SOC Term Classification Code Term Level
20.0 100000004852 10058977 Spastic paresis LLT
Population Age: Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: PL (Completed) Outside EU/EEA
Trial results: View results

EudraCT Number: 2005-003093-21 Sponsor Protocol Number: 20091977 Start Date:
Sponsor Name: Medical Department I
Full Title: Influence of combined therapy of niacin and statins on stem cell mobilization and inflammatory parameters in patients suffering from coronary artery disease – randomized clinical study -
Medical condition: Have stable coronary artery disease (i.e. no acute event like myocardial infarction or PTCA less then 3 months ago)
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: (No results available)
EudraCT Number: 2007-002223-32 Sponsor Protocol Number: E2007-0507 Start Date:
Sponsor Name: Charité Universitaetsmedizin
Full Title: A multicentre, double-blind, randomised placebo-controlled trial of sodium bicarbonate to prevent acute kidney injury in patients undergoing cardiopulmonary bypass surgery.
Medical condition: Cardiac surgical patients in whom the use of cardiopulmonary bypass is planned and having at least one ore more of the following risk factors for post-operative acute kidney injury • Age ≥ 70 years...
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed) IE (Prematurely Ended)
Trial results: View results

EudraCT Number: 2014-001740-38 Sponsor Protocol Number: P130910 Start Date:
Sponsor Name: ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
Full Title:
Medical condition:
Disease: Version SOC Term Classification Code Term Level
18.0 100000004851 10019515 Hemolytic uremic syndrome LLT
Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: FR (Ongoing)
Trial results: (No results available)
EudraCT Number: 2020-004708-32 Sponsor Protocol Number: 232SM302 Start Date:
Sponsor Name: Biogen Idec Research Limited
Full Title: A Long-Term Extension Study of Nusinersen (BIIB058) Administered at Higher Doses in Participants With Spinal Muscular Atrophy Who Previously Participated in an Investigational Study With Nusinersen
Medical condition: Muscular Atrophy, Spinal
Disease: Version SOC Term Classification Code Term Level
20.1 10010331 - Congenital, familial and genetic disorders 10041582 Spinal muscular atrophy PT
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults Gender: Male, Female
Trial protocol: EE (Completed) ES (Ongoing) HU (Ongoing) DE (Ongoing) PL (Completed) IT (Ongoing) NL (Ongoing) FR (Ongoing)
Trial results: (No results available)

EudraCT Number: 2014-003346-27 Sponsor Protocol Number: ATYR1940-C-003 Start Date:
Sponsor Name: ATYR PHARMA, INC.
Full Title: An Open-Label, Intrapatient Dose-Escalation Study to Evaluate the Safety, Tolerability, Immunogenicity, and Biological Activity of ATYR1940 in Patients With Early Onset and Other Pediatric Onset Fa...
Medical condition: Early Onset and Other Pediatric Onset Facioscapulohumeral Muscular Dystrophy
Disease: Version SOC Term Classification Code Term Level
20.0 10010331 - Congenital, familial and genetic disorders 10064087 Facioscapulohumeral muscular dystrophy PT
Population Age: Adolescents, Under 18, Adults Gender: Male, Female
Trial protocol: IT (Prematurely Ended)
Trial results: View results
EudraCT Number: 2009-011095-30 Sponsor Protocol Number: Primo2009 Start Date:
Sponsor Name: Medizinische Fakultät Mannheim, Ruprecht-Karls-Universität Heidelberg
Full Title: Intra-individual comparison of Gd-EOB-DTPA disodium (Primovist) and Gadobutrol (Gadovist) in patients with suspicion of hepatocellular carcinoma
Medical condition: Patients of both genders are eligible for this study in case they present with suspicion of HCC after Gadovist® -enhanced MRI.
Disease: Version SOC Term Classification Code Term Level
12.0 10036706 Primary liver cancer non-resectable LLT
12.0 10036707 Primary liver cancer recurrent LLT
12.0 10036708 Primary liver cancer resectable LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: (No results available)

EudraCT Number: 2011-000989-35 Sponsor Protocol Number: P101001 Start Date:
Sponsor Name: ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
Full Title:
Medical condition:
Disease: Version SOC Term Classification Code Term Level
14.0 10010331 - Congenital, familial and genetic disorders 10066131 Congenital central hypoventilation syndrome PT
Population Age: Adolescents, Under 18, Adults Gender: Female
Trial protocol: FR (Ongoing)
Trial results: (No results available)
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