- Trials with a EudraCT protocol (44,359)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,359 result(s) found.
Displaying page 1,786 of 2,218.
EudraCT Number: 2018-001744-62 | Sponsor Protocol Number: 2018/2727 | Start Date*: 2018-11-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Gustave Roussy | ||||||||||||||||||||||||||||||||||||||
Full Title: A multicenter, open label, phase II basket trial exploring the efficacy and safety of the combination of rucaparib (PARP inhibitor) and atezolizumab (anti-PD-L1 antibody) in patients with DNA repai... | ||||||||||||||||||||||||||||||||||||||
Medical condition: •Molecularly selected cohorts that harbor DNA repair deficiency: –Non-Small Cell Lung Cancer –Urothelial Bladder Cancer –Metastatic Castration Resistant Prostate Cancer –Others: any histology, exce... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002889-41 | Sponsor Protocol Number: UC-BCG-2103 | Start Date*: 2022-04-29 | ||||||||||||||||
Sponsor Name:UNICANCER | ||||||||||||||||||
Full Title: LESS: Single-arm study to de-escalate adjuvant endocrine therapy duration in women with HR+ HER2- breast cancer at very low risk of metastasis | ||||||||||||||||||
Medical condition: Post-menopausal women with localized luminal A breast cancer and considered at low risk of metastatic relapse | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001062-28 | Sponsor Protocol Number: AC-055-312 | Start Date*: 2017-01-25 | |||||||||||
Sponsor Name:ACTELION Pharmaceuticals Ltd | |||||||||||||
Full Title: A multicenter, open-label, randomized, event-driven study to assess efficacy, safety and pharmacokinetics of macitentan versus standard of care in children with pulmonary arterial hypertension | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) AT (Completed) PT (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) FR (Completed) FI (Completed) Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001870-38 | Sponsor Protocol Number: GTi1201 | Start Date*: 2014-01-09 | |||||||||||
Sponsor Name:Grifols Therapeutics Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Two Dose Regimens (60 mg/kg and 120 mg/kg) of Weekly Intravenous Alphal-Proteinase Inhibitor (Human) in Sub... | |||||||||||||
Medical condition: Pulmonary Emphysema due to Alpha-1-Antitrypsin Deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) IE (Completed) EE (Completed) DK (Trial now transitioned) ES (Completed) FI (Trial now transitioned) PL (Trial now transitioned) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001908-38 | Sponsor Protocol Number: R5093-ONC-1863 | Start Date*: 2020-09-28 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A PHASE 1/2 STUDY OF REGN5093 IN PATIENTS WITH MET-ALTERED ADVANCED NON-SMALL CELL LUNG CANCER | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002845-39 | Sponsor Protocol Number: Infmed1 | Start Date*: 2019-10-02 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: Partial oral antibiotic treatment for bacterial brain abscess: An open-label randomised non-inferiority trial (ORAL) | |||||||||||||
Medical condition: Brain abscess | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004393-62 | Sponsor Protocol Number: NBI-921352-DEE2013 | Start Date*: 2022-03-18 | |||||||||||
Sponsor Name:Neurocrine Biosciences, Inc. | |||||||||||||
Full Title: A Prospective, Long-Term, Interventional, Active Extension Study to Evaluate the Safety and Tolerability of NBI-921352 as Adjunctive Therapy in Subjects with SCN8A Developmental and Epileptic Encep... | |||||||||||||
Medical condition: SCN8A Developmental and Epileptic Encephalopathy Syndrome (SCN8ADEE) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) BE (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) FR (Ongoing) IT (Prematurely Ended) DE (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000259-35 | Sponsor Protocol Number: 2020_03 | Start Date*: 2022-04-29 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Lille | |||||||||||||
Full Title: Assessment of the interest of a peri-operative antibiotic strategy applied to patients with asymptomatic bacteriuria undergoing intra-vesical botulinum toxin A injections | |||||||||||||
Medical condition: Overactive bladder (OAB) and/or detrusor overactivity (DO) in multiple sclerosis (MS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001887-31 | Sponsor Protocol Number: RD.06.SPR.118161 | Start Date*: 2020-02-19 | |||||||||||
Sponsor Name:Galderma S.A. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Subjects with Moderate-to-Severe Atopic Dermatitis | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) GB (GB - no longer in EU/EEA) DE (Completed) LT (Completed) NL (Completed) AT (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003525-30 | Sponsor Protocol Number: COLCAD | Start Date*: 2022-01-06 | |||||||||||
Sponsor Name:Aarhus University Hospital, Steno Diabetes Center Aarhus | |||||||||||||
Full Title: Effect of colchicine on cardiovascular target organ damage in patients with type 2 diabetes - A randomized placebo-controlled trial | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000470-36 | Sponsor Protocol Number: SEP361-301 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Sunovion Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Parallel-group, Placebo-controlled, Fixed-dose, Multicenter Study to Evaluate the Efficacy and Safety of SEP-363856 in Acutely Psychotic Subjects with Schizophrenia | ||||||||||||||||||
Medical condition: Schizophrenia | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001501-69 | Sponsor Protocol Number: NN9535-4820 | Start Date*: 2022-07-26 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Investigation of Clinical Comparability of Semaglutide Drug Products Based on the Proposed and the Approved Drug Substance Manufacturing Processes in Participants with Type 2 Diabetes | |||||||||||||
Medical condition: Diabetes mellitus, Type 2 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004750-28 | Sponsor Protocol Number: PropoCon-Pilot | Start Date*: 2021-04-30 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Electrocardiographic And Clinical Effects Of Target-Controlled Infusion Of Propofol In Adults With Brugada Syndrome. A Pilot Study. | ||
Medical condition: Target Controlled Infusion of Propofol in patients with Brugada Syndrome. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-006639-24 | Sponsor Protocol Number: 2020/ABM/01/00080 | Start Date*: 2022-10-19 |
Sponsor Name:The Cardinal Stefan Wyszyński Institute of Cardiology | ||
Full Title: Multicenter Polish Study of the Use of Bromocriptine in Perinatal Cardiomyopathy. New BioMarkers in the Early Diagnosis of Peripartum CardioMyopathy. PolBrom-PPCM | ||
Medical condition: PeriPartum Cardiomiopathy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: PL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004266-18 | Sponsor Protocol Number: LTF-307 | Start Date*: 2020-09-03 | |||||||||||
Sponsor Name:bluebird bio, Inc. | |||||||||||||
Full Title: Long-term Follow-up of Subjects With Sickle Cell Disease Treated With Ex Vivo Gene Therapy Using Autologous Hematopoietic Stem Cells Transduced With a Lentiviral Vector | |||||||||||||
Medical condition: Subjects with sickle-cell disease treated with gene therapy drug products in a bluebird bio-sponsored study will be invited to participate in this long-term follow-up study to monitor the safety an... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000365-41 | Sponsor Protocol Number: CNTO1959UCO3004 | Start Date*: 2023-04-26 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Guselkumab Subcutaneous Induction Therapy in Participants with Mode... | |||||||||||||
Medical condition: Moderately to Severely Active Ulcerative Colitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) BE (Trial now transitioned) CZ (Trial now transitioned) FR (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001639-10 | Sponsor Protocol Number: 787-201 | Start Date*: 2023-06-09 | |||||||||||
Sponsor Name:Intercept Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Dose-escalation, Proof-of-Concept Study Evaluating the Safety, Tolerability, Efficacy and Pharmacokinetics of INT-787 in Subje... | |||||||||||||
Medical condition: Severe Alcohol-Associated Hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006904-34 | Sponsor Protocol Number: CHD21_0121 | Start Date*: 2022-06-23 |
Sponsor Name:Centre Hospitalier Départemental Vendée | ||
Full Title: Evaluation of the interest of perianal infiltration during thermodestruction of haemorrhoidal disease by Radiofrequency (RAFAELO® procedure) | ||
Medical condition: Hemorrhoidal surgery by thermodestruction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002363-26 | Sponsor Protocol Number: NeoCol | Start Date*: 2013-07-23 | |||||||||||
Sponsor Name:Vejle Hospital | |||||||||||||
Full Title: Neoadjuvant chemotherapy versus standard treatment in patients with locally advanced colon cancer | |||||||||||||
Medical condition: Colon cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) SE (Ongoing) NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004651-23 | Sponsor Protocol Number: IJB-SYNERGY-012017 | Start Date*: 2018-10-16 | |||||||||||||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||||||||||||
Full Title: A Phase I/II Study of Paclitaxel plus Carboplatin and Durvalumab (MEDI4736) with or without Oleclumab (MEDI9447) for Previously Untreated Locally Recurrent Inoperable or Metastatic Triple-negative ... | |||||||||||||||||||||||
Medical condition: Previously untreated locally recurrent inoperable or metastatic triple-negative breast cancer (TNBC) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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