Ultime prove


EudraCT Number: 2022-000648-32 Sponsor Protocol Number: SCY-078-302 Start Date: 2023-03-31
Sponsor Name: SCYNEXIS, Inc.
Full Title: A Phase 3, Multicenter, Prospective, Randomized, Double-blind Study of Two Treatment Regimens for Candidemia and/or Invasive Candidiasis: Intravenous Echinocandin followed by Oral Ibrexafungerp ver...
Medical condition: Invasive Candidiasis/ Candidemia
Disease: Version SOC Term Classification Code Term Level
20.0 100000004862 10060573 Candidemia LLT
20.0 100000004862 10064954 Invasive candidiasis LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: GR (Ongoing) ES (Temporarily Halted) BG (Ongoing) IT (Ongoing)
Trial results: (No results available)

EudraCT Number: 2022-003365-38 Sponsor Protocol Number: VTX958-202 Start Date: 2023-03-31
Sponsor Name: Ventyx Biosciences, Inc.
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of VTX958 in Participants with Moderately to Severely Active Crohn’s D...
Medical condition: Moderately to severely active Crohn’s disease
Disease: Version SOC Term Classification Code Term Level
20.0 10017947 - Gastrointestinal disorders 10011401 Crohn's disease PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: SK (Ongoing) LT (Ongoing) DE (Ongoing) HU (Ongoing) IT (Ongoing) PL (Ongoing) BG (Ongoing)
Trial results: (No results available)
EudraCT Number: 2022-002757-26 Sponsor Protocol Number: BH-200-03 Start Date: 2023-03-28
Sponsor Name: HMNC Holding GmbH
Full Title: A 14-week, multicentre, double-blind, randomised, placebo-controlled phase II study with an 8-week treatment period to assess the efficacy and tolerability of a fixed dose of BH-200 (250 mg BID) i...
Medical condition: Major Depressive Disorder
Disease: Version SOC Term Classification Code Term Level
21.1 10037175 - Psychiatric disorders 10057840 Major depression PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: LT (Ongoing) BG (Ongoing) DE (Ongoing) ES (Ongoing)
Trial results: (No results available)

EudraCT Number: 2022-003124-41 Sponsor Protocol Number: 219510 Start Date: 2023-03-27
Sponsor Name: GlaxoSmithKline Biologicals SA
Full Title: A non-randomized, open label, multi-country, cohort study to describe the safety of study participants who received RSVPreF3 maternal vaccination (any dose) or controls from previous RSV MAT studie...
Medical condition: Pregnancy related outcomes and events in maternal participants who were vaccinated against RSV or received control, and in their infants
Disease: Version SOC Term Classification Code Term Level
20.0 10036585 - Pregnancy, puerperium and perinatal conditions 10070538 Gestational hypertension PT
20.0 10036585 - Pregnancy, puerperium and perinatal conditions 10036485 Pre-eclampsia PT
25.0 10036585 - Pregnancy, puerperium and perinatal conditions 10086971 Pre-eclampsia with severe features LLT
20.0 10036585 - Pregnancy, puerperium and perinatal conditions 10070532 Fetal growth restriction LLT
20.0 10036585 - Pregnancy, puerperium and perinatal conditions 10073024 Preterm premature rupture of membranes PT
21.1 10036585 - Pregnancy, puerperium and perinatal conditions 10075863 Preterm labor LLT
21.1 10036585 - Pregnancy, puerperium and perinatal conditions 10018210 Gestational diabetes mellitus LLT
20.0 100000004862 10008755 Chorioamnionitis LLT
21.1 10036585 - Pregnancy, puerperium and perinatal conditions 10041093 Small for gestational age LLT
21.1 10036585 - Pregnancy, puerperium and perinatal conditions 10067508 Low birth weight baby PT
21.1 10036585 - Pregnancy, puerperium and perinatal conditions 10067509 Very low birth weight baby LLT
21.1 10036585 - Pregnancy, puerperium and perinatal conditions 10074164 Extremely low birth weight baby LLT
20.1 10018065 - General disorders and administration site conditions 10011912 Death neonatal PT
25.0 10042613 - Surgical and medical procedures 10086969 Medically induced preterm birth PT
Population Age: Children, Adolescents, Under 18, Adults Gender: Female
Trial protocol: FI (Ongoing) BE (Ongoing) FR (Ongoing) ES (Ongoing)
Trial results: (No results available)
EudraCT Number: 2022-002389-33 Sponsor Protocol Number: CNTO1959CRD3007 Start Date: 2023-03-27
Sponsor Name: Janssen-Cilag International NV
Full Title: A Randomized, Double-blind, Placebo-controlled Study Evaluating the Safety and Efficacy of Guselkumab for the Treatment of Participants with Crohn’s Disease After Surgical Resection
Medical condition: Crohn’s Disease After Surgical Resection
Disease: Version SOC Term Classification Code Term Level
20.0 10017947 - Gastrointestinal disorders 10011401 Crohn's disease PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: ES (Temporarily Halted) HU (Ongoing)
Trial results: (No results available)

EudraCT Number: 2022-002792-11 Sponsor Protocol Number: KAN0007 Start Date: 2023-03-27
Sponsor Name: Kancera AB
Full Title: KANDOVA - A two-part Phase Ib/IIa study to evaluate the safety and tolerability of KAND567, in combination with carboplatin therapy, and to determine the Recommended Phase II Dose (RPIID) of KAND56...
Medical condition: Recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer.
Disease: Version SOC Term Classification Code Term Level
20.0 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10033128 Ovarian cancer PT
Population Age: Adults, Elderly Gender: Female
Trial protocol: NO (Ongoing)
Trial results: (No results available)
EudraCT Number: 2022-003628-42 Sponsor Protocol Number: NBK182/1/2022 Start Date: 2023-03-24
Sponsor Name: Medical University of Gdańsk
Full Title: A Randomized, Double-Blind, Placebo-Controlled Multicenter Study of Levosimendan Therapy in low ejection fraction Takotsubo Syndrome (LevoTako Trial)
Medical condition: Takotsubo syndrome (TTS), also known as apical ballooning syndrome, Takotsubo cardiomyopathy, broken heart syndrome, and stress-induced cardiomyopathy, is a rare condition and accounts for 1–3% of ...
Disease: Version SOC Term Classification Code Term Level
20.1 100000004849 10067676 Takotsubo syndrome LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: PL (Ongoing)
Trial results: (No results available)

EudraCT Number: 2022-002959-18 Sponsor Protocol Number: PRN1008-017/ACT17125 Start Date: 2023-03-23
Sponsor Name: Principia Biopharma Inc
Full Title: An open label, two-arm, Phase 2a study to evaluate the effect of rilzabrutinib (PRN1008/SAR444671) on safety and disease activity in patients with IgG4-related disease
Medical condition: IgG4-related disease
Disease: Version SOC Term Classification Code Term Level
20.0 10028395 - Musculoskeletal and connective tissue disorders 10077271 Immunoglobulin G4 related disease PT
Population Age: Adults Gender: Male, Female
Trial protocol: ES (Prematurely Ended)
Trial results: (No results available)
EudraCT Number: 2021-004849-20 Sponsor Protocol Number: 283PD201 Start Date: 2023-03-22
Sponsor Name: Biogen Idec Research Limited
Full Title: A Phase 2b, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Determine the Efficacy and Safety of BIIB122 in Participants with Parkinson’s Disease
Medical condition: Parkinson's Disease
Disease: Version SOC Term Classification Code Term Level
20.0 10029205 - Nervous system disorders 10061536 Parkinson's disease PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Ongoing) ES (Ongoing) FR (Ongoing) NL (Ongoing) AT (Ongoing) PL (Ongoing) IT (Ongoing)
Trial results: (No results available)

EudraCT Number: 2023-000150-20 Sponsor Protocol Number: 1 Start Date: 2023-03-22
Sponsor Name: Bispebjerg-Frederiksberg Hospital
Full Title: The effect of exercise on pharmacodynamics and pharmacokinetics of a single dose of unfractionated heparin: A randomized, controlled, cross-over study
Medical condition: Unfractionated heparin is used for the prevention and treatment of deep vein thrombosis and complications hereof
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults Gender: Male
Trial protocol: DK (Completed)
Trial results: (No results available)
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