- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: RNA transcription.
Displaying page 1 of 2.
| EudraCT Number: 2013-004747-23 | Sponsor Protocol Number: BPC01-001 | Start Date*: 2014-01-17 | |||||||||||
| Sponsor Name:Bionor Pharma ASA | |||||||||||||
| Full Title: An Open Phase I/IIa Study to Evaluate the Safety and Effect of Therapeutic HIV-1 Immunization using Vacc-4x + rhuGM-CSF, and HIV-1 Reactivation using Romidepsin, on the Viral Reservoir in Virologic... | |||||||||||||
| Medical condition: HIV-infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003215-66 | Sponsor Protocol Number: MARAVITRANS | Start Date*: 2012-09-26 |
| Sponsor Name:FIBio Hospital Universitario Ramón y Cajal | ||
| Full Title: EFFECT OF MARAVIROC ON THE TRANSCRIPTION OF THE HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV-1) IN RESTING CD4+ T LYMPHOCYTES IN PATIENTS ON ANTIRETROVIRAL TREATMENT WITH SUPPRESSED VIRAL LOAD | ||
| Medical condition: HIV-infected patients | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001224-33 | Sponsor Protocol Number: COV-HCQ | Start Date*: 2020-03-25 | |||||||||||
| Sponsor Name:Universitätsklinikum Tübingen | |||||||||||||
| Full Title: Randomized controlled trial of hydroxychloroquine versus placebo for the treatment of adult patients with acute coronavirus disease 2019 – COVID-19 | |||||||||||||
| Medical condition: Acute coronavirus disease 2019 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000533-22 | Sponsor Protocol Number: VX-950-TiDP24-C216 | Start Date*: 2008-11-14 | |||||||||||
| Sponsor Name:Tibotec BVBA | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, Phase III trial of 2 regimens of telaprevir (with and without delayed start) combined with pegylated interferon alfa-2a (Pegasys®) and ribavirin (Cop... | |||||||||||||
| Medical condition: Chronic genotype 1 Hepatitis C infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) SE (Completed) FR (Completed) AT (Completed) IT (Completed) GB (Completed) ES (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001026-22 | Sponsor Protocol Number: 1813T0835 | Start Date*: 2021-03-05 |
| Sponsor Name:Shionogi & Co., Ltd. | ||
| Full Title: An Open-label Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Baloxavir Marboxil 2% Granules after Administration of a Single Dose to Otherwise Healthy Pediatric Patient... | ||
| Medical condition: Influenza | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004189-33 | Sponsor Protocol Number: REK322442 | Start Date*: 2013-11-28 |
| Sponsor Name:Haukeland University Hospital | ||
| Full Title: ULTRADIAN SUBCUTANEOUS HYDROCORTISONE (USHI) INFUSION IN ADDISON’S DISEASE | ||
| Medical condition: Addison`s disease | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000240-94 | Sponsor Protocol Number: CLEAR0001 | Start Date*: 2012-05-09 | ||||||||||||||||
| Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
| Full Title: The Safety and Efficacy of The Histone Deacetylase Inhibitor Panobinostat for Purging HIV-1 from The Latent Reservoir (CLEAR) Study | ||||||||||||||||||
| Medical condition: Human Immunodeficiency Virus (HIV) Infection | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-003419-68 | Sponsor Protocol Number: HepBTer | Start Date*: 2020-12-18 | |||||||||||||||||||||||||||||||
| Sponsor Name:Academic Medical Center (AMC) | |||||||||||||||||||||||||||||||||
| Full Title: From fungus to virus, a phase 2a clinical trial investigating the safety and efficacy of terbinafine in chronic hepatitis B patients | |||||||||||||||||||||||||||||||||
| Medical condition: Chronic hepatitis B infection | |||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-005015-40 | Sponsor Protocol Number: IVER-303 | Start Date*: 2021-04-29 | |||||||||||
| Sponsor Name:Chemo Research S.L. | |||||||||||||
| Full Title: A multicentre, phase III, double-blind, randomised, parallel, placebo-controlled trial to assess efficacy and safety of early administration of Ivermectin during 3 consecutive days to prevent SARS ... | |||||||||||||
| Medical condition: Coronavirus disease (COVID-19) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002927-39 | Sponsor Protocol Number: BOOST_TX/RESCUE_TX | Start Date*: 2021-06-13 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Preventive strategies against SARS-CoV-2 in kidney transplant recipients: Intervention A – vaccination: Single blinded randomized controlled trial on BNT162b2 or mRNA-1273 (mRNA) vs Ad26COVS1 or C... | ||
| Medical condition: Intervention A - vaccination Patients following kidney transplant recipients who do not have an adequate immune response against SARS-CoV-2 following two doses of an mRNA vaccine Substudy A: kidne... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001966-13 | Sponsor Protocol Number: EDP938-201 | Start Date*: 2021-07-07 | |||||||||||
| Sponsor Name:Enanta Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, 2-PART STUDY TO EVALUATE EDP-938 REGIMENS IN SUBJECTS AGED 28 DAYS TO 36 MONTHS INFECTED WITH RESPIRATORY SYNCYTIAL VIRUS (RSV) | |||||||||||||
| Medical condition: Respiratory Syncytial Virus (RSV) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) PL (Completed) ES (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002154-70 | Sponsor Protocol Number: CP40559 | Start Date*: 2019-10-24 | ||||||||||||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
| Full Title: A MULTICENTER, SINGLE-ARM, OPEN-LABEL STUDY TO ASSESS THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF BALOXAVIR MARBOXIL IN OTHERWISE HEALTHY PEDIATRIC PATIENTS FROM BIRTH TO LESS THAN 1 YEAR WITH IN... | ||||||||||||||||||||||||||||
| Medical condition: Influenza | ||||||||||||||||||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: PL (Completed) ES (Ongoing) FI (Completed) BG (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-001529-30 | Sponsor Protocol Number: EDP938-102 | Start Date*: 2020-09-29 | |||||||||||
| Sponsor Name:Enanta Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study of EDP-938 Administered Orally for the Treatment of Acute Upper Respiratory Tract Infection with Respiratory Syncytial Virus in Ambula... | |||||||||||||
| Medical condition: Respiratory syncytial virus (RSV) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) NL (Completed) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002139-94 | Sponsor Protocol Number: IPH1101-203 | Start Date*: 2007-06-19 | |||||||||||
| Sponsor Name:Innate Pharma | |||||||||||||
| Full Title: Multiple dose Phase II study of IPH1101 in monotherapy or associated with a low dose of IL2 (2MIU) in non previously treated hepatitis C patients | |||||||||||||
| Medical condition: Non previously treated Hepatitis C patients | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-003836-77 | Sponsor Protocol Number: OCTO-003 | Start Date*: 2008-12-09 |
| Sponsor Name:University of Oxford | ||
| Full Title: AspECT - A phase III, randomised study of aspirin and esomeprazole chemoprevention in Barrett's metaplasia & oesophagitis. | ||
| Medical condition: Barrett's Metaplasia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001684-89 | Sponsor Protocol Number: RG_20-030 | Start Date*: 2020-05-05 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: CATALYST - A randomised phase II proof of principle multi-arm multi-stage trial designed to guide the selection of interventions for phase III trials in hospitalised patients with COVID-19 infection. | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004971-30 | Sponsor Protocol Number: FLUGEN-H3N2-V002 | Start Date*: 2018-04-27 | |||||||||||
| Sponsor Name:FluGen, Inc | |||||||||||||
| Full Title: A Phase 2a Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Safety, Immunogenicity, and Efficacy of Bris10 M2SR (H3N2 A/Brisbane/10/2007) Vaccine Administered as a Single Intranas... | |||||||||||||
| Medical condition: Prophylactic H3N2(A/Brisbane/10/2007) monovalent influenza vaccine, Bris10 M2SR, for protection against influenza disease caused by seasonal influenza A viruses. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000338-16 | Sponsor Protocol Number: 42847922MDD3002 | Start Date*: 2020-10-27 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, Study to Evaluate the Efficacy and Safety of Seltorexant 20 mg as Adjunctive Therapy to Antidepressants in Adult and Eld... | |||||||||||||
| Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) FI (Prematurely Ended) PL (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000641-33 | Sponsor Protocol Number: PAX | Start Date*: 2022-04-21 | |||||||||||
| Sponsor Name:Fundació FLS de Lluita contra la Sida, les Malalties Infeccioses i la Promoció de la Salut i La Ciència | |||||||||||||
| Full Title: Plasma Exchange Therapy for Post- COVID-19 Condition: A Pilot, Randomized Double-Blind Study | |||||||||||||
| Medical condition: Post-Acute-Covid-19 Syndrome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012280-34 | Sponsor Protocol Number: 26866138-LYM-2034 | Start Date*: 2009-12-04 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Randomized, Open-Label, Multicenter, Phase 2 Study of the Combination of VELCADE, Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone (VR-CAP) or Rituximab, Cyclophosphamide, Doxorubicin, ... | |||||||||||||
| Medical condition: Non-Germinal Center B-Cell Subtype of Diffuse Large B-Cell Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) PT (Completed) CZ (Completed) DE (Completed) FR (Completed) ES (Completed) IT (Completed) IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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