- Trials with a EudraCT protocol (339)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (16)
339 result(s) found for: Ritonavir.
Displaying page 1 of 17.
EudraCT Number: 2022-002827-36 | Sponsor Protocol Number: C4671042 | Start Date*: 2023-02-10 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: AN INTERVENTIONAL, EFFICACY AND SAFETY, PHASE 2, RANDOMIZED, DOUBLE-BLIND, 2-ARM STUDY TO INVESTIGATE A REPEAT 5-DAY COURSE OF NIRMATRELVIR/RITONAVIR COMPARED TO PLACEBO/RITONAVIR IN PARTICIPANTS A... | |||||||||||||
Medical condition: SARS-CoV-2 Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000604-88 | Sponsor Protocol Number: SSAT028 | Start Date*: 2008-04-04 |
Sponsor Name:St Stephen's Aids Trust | ||
Full Title: A phase IV, two-arm, open-label, single-centre randomised pilot study to assess the feasibility of immeidate or deferred switching of HIV-infected individuals intolerant of efavirenz, ritonavir-boo... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000649-11 | Sponsor Protocol Number: SSAT046 | Start Date*: 2012-08-22 |
Sponsor Name:St Stephen's Aids Trust | ||
Full Title: A phase IV, open-label, single centre, single-arm, pilot study to assess Cerebrospinal fluid INflammatory markers after Addition of Maraviroc to MONotherapy darunavir/ritonavir – The CINAMMON Study... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-013287-39 | Sponsor Protocol Number: LOPIDAR | Start Date*: 2009-09-25 | |||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
Full Title: RANDOMISED AND PROSPECTIVE CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LOPINAVIR/RITONAVIR MONOTHERAPY VS DARUNAVIR/RITONAVIR MONOTHERAPIES AS SIMPLIFICATION SWITCHING STRATEGIES OF PI/NN... | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002700-78 | Sponsor Protocol Number: DDD16RITONAVIR | Start Date*: 2016-10-28 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Supersaturation and precipitation of ritonavir in the gastrointestinal tract of healthy volunteers | ||
Medical condition: Healthy human volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-000932-19 | Sponsor Protocol Number: SSAT 022 | Start Date*: 2008-02-25 |
Sponsor Name:St Stephen's AIDS Trust | ||
Full Title: A phase IV study to assess the feasibility of substituting double ritonavir-boosted protease inhibitors (PI) with ritonavir-boosted darunavir (DRV/r) in HIV-infected individuals with viral suppress... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004844-59 | Sponsor Protocol Number: CAEB071A2117 | Start Date*: 2008-01-31 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A two part, randomized, placebo controlled study to evaluate the pharmacokinetics and cardiovascular pharmacodynamics of AEB071 in combination with ritonavir in healthy volunteers | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004430-41 | Sponsor Protocol Number: SSAT 013 | Start Date*: 2005-11-04 |
Sponsor Name:St Stephen's AIDS Trust | ||
Full Title: Effect of food on the pharmacokinetic profile of saquinavir at steady state in HIV-infected patients treated with saquinavir/ritonavir 1000/100 mg b.i.d. | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005609-76 | Sponsor Protocol Number: SSAT 018 | Start Date*: 2006-11-28 |
Sponsor Name:St Stephens Aids Trust | ||
Full Title: EFFECT OF DIFFERENT MEALS ON THE PHARMACOKINETIC PROFILE OF SAQUINAVIR AT STEADY STATE IN HIV-INFECTED PATIENTS TREATED WITH SAQUINAVIR/RITONAVIR 1000/100 mg BID. | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002447-22 | Sponsor Protocol Number: C4671031 | Start Date*: 2022-11-21 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 2, DOUBLE BLIND, 2 ARM STUDY TO INVESTIGATE ORALLY ADMINISTERED NIRMATRELVIR/RITONAVIR COMPARED WITH PLACEBO/RITONAVIR FOR THE TREATMENT OF SEVERE COVID... | |||||||||||||
Medical condition: SARS-CoV-2 Infection | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002864-24 | Sponsor Protocol Number: UMCN-AKF 06.02 | Start Date*: 2006-09-25 | |||||||||||
Sponsor Name:Dept. of Clinical Pharmacy, Radboud UMC Nijmegen, The Netherlands | |||||||||||||
Full Title: Drug interactions between ATOvaquone used in MAlaria prophylaxis and antiretroviral agents in HIV-1 infected patients (ATOMA) | |||||||||||||
Medical condition: malaria prophylaxis in HIV patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001913-14 | Sponsor Protocol Number: SSAT043 | Start Date*: 2011-11-08 |
Sponsor Name:St Stephen's Aids Trust | ||
Full Title: A randomized crossover study of the effects of zinc sulphate supplementation on atazanavir/ritonavir-associated hyperbilirubinemia | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004854-12 | Sponsor Protocol Number: N19RER | Start Date*: 2019-04-12 | |||||||||||
Sponsor Name:Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | |||||||||||||
Full Title: An Open-label Single-arm Pharmacokinetic Trial, Investigating the Effect of CYP3A4 inhibitor Ritonavir on the Pharmacokinetics of Erlotinib | |||||||||||||
Medical condition: Advanced EGFR mutation positive non small cell lung cancer, pancreatic carcinoma, colorectal cancer and biliary cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013648-35 | Sponsor Protocol Number: PENTA 18 | Start Date*: 2010-06-23 | |||||||||||
Sponsor Name:PENTA Foundation | |||||||||||||
Full Title: KONCERT A Kaletra ONCE daily Randomised Trial of the pharmacokinetics, safety and efficacy of twice-daily versus once-daily lopinavir/ritonavir tablets dosed by weight as part of combination antir... | |||||||||||||
Medical condition: Paediatric HIV-1 Infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) NL (Ongoing) FR (Completed) GB (Completed) ES (Completed) PT (Completed) BE (Completed) DE (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2011-005981-39 | Sponsor Protocol Number: KMON | Start Date*: 2012-03-20 |
Sponsor Name:Unidad de VIH. Servicio de Enfermedades Infecciosas. Hospital de Bellvitge | ||
Full Title: Pilot simplification study to Lopinavir/ritonavir 800/200 mg monotherapy regimen once daily | ||
Medical condition: HIV-1 positive patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021159-25 | Sponsor Protocol Number: SILIDAR | Start Date*: 2010-11-08 | |||||||||||
Sponsor Name:Fundació Lluita contra la Sida | |||||||||||||
Full Title: INTERACCIONES FARMACOLÓGICAS ENTRE LA SILIMARINA Y DARUNAVIR/RITONAVIR | |||||||||||||
Medical condition: Infección por el VIH. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003077-15 | Sponsor Protocol Number: EIG-LNF-002 | Start Date*: 2015-11-23 |
Sponsor Name:Eiger BioPharmaceuticals | ||
Full Title: A Phase 2, Open-Label Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamic Activity of Titrating-Dose Lonafarnib in Combination with Ritonavir in Patients Chronically Infected w... | ||
Medical condition: Chronic Hepatitis D Virus (HDV) Infection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002663-10 | Sponsor Protocol Number: SSAT049 | Start Date*: 2012-11-12 |
Sponsor Name:St Stephen's AIDS Trust | ||
Full Title: A phase IV, open-label single-arm study investigating the pharmacokinetics and pharmacodynamics of the antiretroviral combination of rilpivirine and ritonavir-boosted darunavir in therapy-naive HIV... | ||
Medical condition: HIV-1 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002585-19 | Sponsor Protocol Number: MV20507 | Start Date*: 2006-08-02 | |||||||||||
Sponsor Name:Royal Free Hampstead NHS Trust | |||||||||||||
Full Title: A 24-week, randomised, open-label, 2-arm study to compare the tolerability and efficacy of saquinavir tablets with ritonavir versus lopinavir/ritonavir tablets in HIV 1 infected adults switching fr... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) Type-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013265-26 | Sponsor Protocol Number: EQUIDAR | Start Date*: 2009-11-11 | |||||||||||
Sponsor Name:Fundació Lluita contra la Sida | |||||||||||||
Full Title: INTERACCIONES FARMACOLÓGICAS ENTRE ECHINACEA PURPUREA Y DARUNAVIR/RITONAVIR | |||||||||||||
Medical condition: Infección por VIH | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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