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Drug or intervention

Ribavirin Clinical Trials

Studies that test Ribavirin, alone, with other treatments or as the comparison.

1,102 registered studies

In numbers

Open to volunteers
7
Active
8
With results posted
470
All registered
1,102

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 7
  • Coronavirus Infection (COVID-19), Pulmonary Arterial Hypertension

    Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS)

    • Recruiting
    • Age: 0 to 20 years
    • Observational study

    The study investigators are interested in learning more about how drugs, that are given to children by their health care provider, act in the bodies of children and young adults in hopes to find the most safe and effective dose…

    Conditions
    Coronavirus Infection (COVID-19), Pulmonary Arterial Hypertension, Urinary Tract Infections in Children, Hypertension
    Trial name
    POPS or POP02 (NCT04278404)
    Testing
    The POP02 study is collecting bodily fluid samples (i.e., whole blood, effluent samples) of children prescribed the following drugs of interest per standard of care:
    Where
    52 sites in United States, Canada
    Volunteers
    5,000 people, healthy volunteers welcome
    Sponsor
    Duke University
  • HCV Infection ( Genotype 4) in CKD Patients

    Treatment of CKD Patients With HCV

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 2/3

    The goal of this clinical trial is to evaluate the optimal drug therapy of HCV in CKD Patients different stages with or without compensated cirrhosis.

    Trial name
    HCV/CKD (NCT07770984)
    Testing
    SOF+DCV, OBV/PTV/r) ± ribavirin (RBV)
    Where
    Egypt
    Volunteers
    50 people
    Sponsor
    Tanta University
    Can I take part? HCV/CKD
  • Crimean-Congo Hemorrhagic Fever

    UMIT-2 - Adaptive Phase IIb Platform Trial to Determine the Efficacy and Safety of Therapeutics for CCHF

    • Recruiting
    • Age: 18 years and older
    • Phase 2

    CCHF has a wide geographical distribution with cases mainly occurring in Asia, the Middle East, South-Eastern Europe and Africa.

    Trial name
    UMIT-2 (NCT06860334)
    Testing
    Favipiravir, Ribavin, Optimised Standard of Care
    Where
    3 sites in Turkey (Türkiye)
    Volunteers
    378 people
    Sponsor
    Liverpool School of Tropical Medicine
    Can I take part? UMIT-2
  • Lassa Fever

    ISTH/ANRS 0409s INTEGRATE Lassa Fever Study

    • Recruiting
    • Age: 18 years and older
    • Phase 2/3

    Lassa fever (LF) is a viral haemorrhagic fever responsible of 5000 deaths per year in West Africa, with in-hospital mortality at 12%.

    Trial name
    NCT06212336
    Testing
    Favipiravir, Ribavirin, Dexamethasone
    Where
    4 sites in Liberia, Nigeria
    Volunteers
    1,755 people
    Sponsor
    Irrua Specialist Teaching Hospital
  • Respiratory Syncytial Virus, Respiratory Syncytial Virus, Human

    Assessing Antiviral Treatments in Early Symptomatic RSV

    • Recruiting
    • Age: 18 to 64 years
    • Phase 2

    This trial will use a previously validated platform, to quantitatively assess antiviral effects in low-risk patients with high viral burdens and uncomplicated Respiratory Syncytial Virus (RSV), to determine in-vivo antiviral…

    Trial name
    ARSYNAL-FC (NCT06488300)
    Testing
    Ribavirin, Molnupiravir, Favipiravir
    Where
    2 sites in Laos, Thailand
    Volunteers
    1,000 people
    Sponsor
    University of Oxford
    Can I take part? ARSYNAL-FC
  • Lassa Fever

    LAssa Fever Adjunct Treatment With DEXamethasone

    • Recruiting
    • Age: 18 years and older
    • Phase 2

    Dexamethasone is a corticosteroid which can modulate inflammatory-mediated tissue damage associated with a wide range of infectious diseases.

    Trial name
    LADEX (NCT06222723)
    Testing
    Dexamethasone, Ribavirin
    Where
    Nigeria
    Volunteers
    42 people
    Sponsor
    Bernhard Nocht Institute for Tropical Medicine
    Can I take part? LADEX
  • Chronic Hepatitis C, Medication Reaction

    The Efficacy of Vosevi in Treating DAA-experienced Patients

    • Recruiting
    • Age: 20 to 70 years
    • Observational study
    • Pill or oral medicine

    Hepatitis C virus (HCV) infection remains a significant health problem in our country. The World Health Organization estimated that 71 million people worldwide had chronic HCV infection in 2015.

    Trial name
    NCT06180590
    Testing
    Sofosbuvir / Velpatasvir / Voxilaprevir Oral Tablet [Vosevi]
    Where
    China
    Volunteers
    200 people
    Sponsor
    The Third Affiliated Hospital of Guangzhou Medical University
    Can I take part? NCT06180590

Completed, with results posted

All 427

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