- Trials with a EudraCT protocol (191)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (78)
191 result(s) found for: Nucleoside.
Displaying page 1 of 10.
EudraCT Number: 2006-006076-38 | Sponsor Protocol Number: RLBUHT3173 | Start Date*: 2007-04-26 |
Sponsor Name:University of Liverpool [...] | ||
Full Title: The Liverpool HIV TDM Registry: Studying influences upon plasma HIV drug exposure | ||
Medical condition: Pharmacogenetic study of HIV+ patients receiving antiretroviral therapy. We wish to correlate drug concentration with host genetic patients receiving certain HIV drugs. No dosage modification wil... | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003425-81 | Sponsor Protocol Number: RLBUHT2763 | Start Date*: 2007-03-29 |
Sponsor Name:University of Liverpool | ||
Full Title: Host genetic factors influencing drug disposition and response to HIV treatment | ||
Medical condition: Pharmacogeneric study of HIV+ patients receiving antiretroviral therapy. We wish to correlate drug concentration with host genetic patients receiving certain HIV drugs. No dosage modification will... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-004788-29 | Sponsor Protocol Number: Covid_vacc_THL2021 | Start Date*: 2021-12-23 | |||||||||||
Sponsor Name:Finnish Institute for Health and Welfare | |||||||||||||
Full Title: COVID-19 vaccine immunological studies in Finland | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001993-52 | Sponsor Protocol Number: IMCOVAS | Start Date*: 2021-05-20 |
Sponsor Name:University of Antwerp | ||
Full Title: Assessment of the immunogenicity and safety of marketed vaccines for COVID-19 after regular schedule and adapted vaccine schedules and routes: BNT162b2 (Comirnaty®; Pfizer-BioNTech), mRNA-1273 Vacc... | ||
Medical condition: Coronavirus disease-19 (COVID-19) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006174-19 | Sponsor Protocol Number: SSAT 019 | Start Date*: 2006-12-12 |
Sponsor Name:St Stephens AIDS Trust | ||
Full Title: A randomised, open label, phase IV comparative study to determine the effects on renal function of continuing treatment with tenofovir versus replacement with abacavir in HIV positive persons | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000880-63 | Sponsor Protocol Number: na | Start Date*: 2021-03-11 |
Sponsor Name:Skåne University Hospital, department of rheumatology in Lud and Malmö | ||
Full Title: COVID-19 vaccine in patients with inflammatory rheumatic diseases: The impact of immunomodulating treatments on the antibody response, T cells response and protection against infection (COVID19-REUMA) | ||
Medical condition: rheumatoid arthritis, SLE, systemic vasculitis, systemic sclerosis, spondylarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004021-26 | Sponsor Protocol Number: RRK 2768 | Start Date*: 2005-10-06 |
Sponsor Name:University Hospital Birmingham | ||
Full Title: Longitudinal relationship between lipodystrophy and adipocyte mitochondria DNA in HIV Patients: comparison between Efavirenz (Sustiva) plus AZT/3TC (Combivir) and a less mitochrondial DNA-toxic reg... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000028-17 | Sponsor Protocol Number: MAINTAINAVIR | Start Date*: 2005-05-10 |
Sponsor Name:DAVID DALMAU | ||
Full Title: Eficacia virológica, inmunológica y trascendencia clínica del efecto de la lamivudina en pacientes portadores de la mutación M184V/I con fracaso terapéutico. | ||
Medical condition: HIV INFECTION | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000893-27 | Sponsor Protocol Number: SJ2021016 | Start Date*: 2021-04-27 |
Sponsor Name:AZ Sint-Jan Brugge-Oostende AV | ||
Full Title: COVID-19: study to detect transfer of SARS-Cov-2 antibodies in breastmilk | ||
Medical condition: pregnancy lactating mothers | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003284-22 | Sponsor Protocol Number: AI463080 | Start Date*: 2007-03-19 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Randomized, Observational Study of Entecavir to Assess Long-term Outcomes Associated with Nucleoside/Nucleotide Monotherapy for Patients with Chronic HBV Infection: The REALM Study | |||||||||||||
Medical condition: CHRONIC HEPATITIS B VIRUS INFECTION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) IT (Completed) PT (Completed) GR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002174-52 | Sponsor Protocol Number: APHP210605 | Start Date*: 2021-05-19 |
Sponsor Name:Assistance Publique -Hopitaux de Paris | ||
Full Title: | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000901-31 | Sponsor Protocol Number: 18122006 | Start Date*: 2007-05-15 |
Sponsor Name:Universitair Ziekenhuis Antwerpen | ||
Full Title: A DOUBLE-BLIND? PLACEBO-CONTROLLED PARALLEL ARM TRIAL TO STUDY THE EFFICACY OF A SINGLE ORAL DOSE OF THE NUCLEOSIDE TRANSPORT INHIBITOR DIPYRIDAMOLE FOR PAIN RELIEF IN PATIENTS AFTER THIRD MOLAR SU... | ||
Medical condition: Pain after third molar surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004889-35 | Sponsor Protocol Number: UCDCRC/21/10 | Start Date*: 2021-12-08 | ||||||||||||||||
Sponsor Name:University College Dublin | ||||||||||||||||||
Full Title: An International Multicentre, Phase 2, Randomised, Adaptive Protocol to determine the need for, optimal timing of and immunogenicity of administering a booster mRNA vaccination dose against SARS-Co... | ||||||||||||||||||
Medical condition: Severe Acute Respiratory Syndrome Coronavirus 19 (COVID-19/SARS-CoV-2) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) NO (Completed) DE (Completed) ES (Ongoing) BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005127-34 | Sponsor Protocol Number: 0518-018 | Start Date*: 2006-03-14 | |||||||||||
Sponsor Name:Merck & Co. Inc. | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Antiretroviral Activity of MK-0518 in Combination With an Optimized Background Therapy (OBT), Versus Opt... | |||||||||||||
Medical condition: Unspecified human immuno-deficiency virus [HIV] disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) ES (Completed) PT (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003386-35 | Sponsor Protocol Number: INSIGHT-016 | Start Date*: 2021-09-01 | |||||||||||
Sponsor Name:Regents of the University of Minesota | |||||||||||||
Full Title: SARS-CoV-2 vaccination strategies in previous hospitalised and recovered COVID-19 patients | |||||||||||||
Medical condition: Participants of the ACTIV-3/TICO clinical trial at selected sites who received certain pre-specified blinded investigational agents or placebo as part of that trial, and who have since achieved sus... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000724-34 | Sponsor Protocol Number: Nuc-STOP | Start Date*: 2018-07-02 | |||||||||||
Sponsor Name:Oslo University Hospital HF | |||||||||||||
Full Title: Norwegian Nucleoside Analogue Stop Study (Nuc-STOP) - A randomized open-label trial in HBeAg negative chronic hepatitis B, aiming at achieving a functional Cure | |||||||||||||
Medical condition: HBeAg negative chronic hepatitis B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004297-42 | Sponsor Protocol Number: IN-NL-2641449 | Start Date*: 2015-06-15 |
Sponsor Name:UMC Utrecht | ||
Full Title: Effect of Switching Atripla to Eviplera on neurocognitive and emotional functioning | ||
Medical condition: neurocognitive and emotional functioning in HIV positive men using antiretroviral therapy | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002327-38 | Sponsor Protocol Number: NL77670.029.21 | Start Date*: 2021-05-26 | ||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||
Full Title: PREGCOVAC-19: the follow up of pregnant women who received COVID-19 vaccination in the Dutch national vaccination program | ||||||||||||||||||
Medical condition: Pregnant women aged ≥ 18 years who are scheduled for COVID-19 vaccination within the Dutch national vaccination program with any of the currently or future available vaccines that are used for preg... | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005119-76 | Sponsor Protocol Number: AI424-227 | Start Date*: 2006-05-24 |
Sponsor Name:Bristol-Myers Squibb S.A. | ||
Full Title: Phase IIIb Multicenter, Single Arm, Open-label Pilot Study to Evaluate the Effectiveness and Safety of Maintenance with Atazanavir/ritonavir as Single Enhanced Protease Inhibitor Therapy in HIV-Inf... | ||
Medical condition: HIV-Infected Patients Evidencing Virologic Suppression Pacientes infectados de VIH, con supresión virológica evidente | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015968-34 | Sponsor Protocol Number: FHCRC1840 | Start Date*: 2010-03-08 | |||||||||||
Sponsor Name:FRED HUTCHINSON CANCER RESEARCH CENTER | |||||||||||||
Full Title: Nonmyeloablative Conditioning with Pre- and Post-Transplant Rituximab followed by Related or Unrelated Donor Hematopoietic Cell Transplantation for Patients with Advanced Chronic Lymphocytic Leukem... | |||||||||||||
Medical condition: Chronic lymphocytic leukemia (CLL) is a malignant disease. CLL is the most common form of leukemia in western countries. Median age at diagnosis is 70 years, and only 10-15% of patients are younger... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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