AzTrials
AzTrials

Drug or intervention

Ritonavir Clinical Trials

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

1,181 registered studies

In numbers

Open to volunteers
32
Active
37
With results posted
359
All registered
1,181

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

Open to volunteers

All 32
  • Advanced Solid Tumors

    A Phase 1/2a Study of DB-1311/BNT324 in Advanced/Metastatic Solid Tumors

    • Recruiting
    • Age: 18 years and older
    • Phase 1/2
    • Pill or oral medicine

    This is a dose-escalation and dose-expansion Phase 1/2a trial to evaluate the safety and tolerability of DB-1311/BNT324 in subjects with advanced solid tumors.

    Trial name
    NCT05914116
    Testing
    DB-1311, Lopinavir and Ritonavir Tablets, itraconazole
    Where
    107 sites in United States, Australia and 2 more
    Volunteers
    862 people
    Sponsor
    DualityBio Inc.
    Can I take part? NCT05914116
  • Human Papilloma Virus (HPV), High-risk Human Papillomavirus Infection

    A Study of the Preliminary Efficacy of DARE-HPV to Treat High-risk Persistent Human Papillomavirus (hrHPV)

    • Recruiting
    • Age: 22 to 50 years
    • Phase 2

    The goal of this clinical study is to learn if DARE-HPV can treat persistent high-risk human papillomavirus (hrHPV). The primary outcome will be if the genital infection clears following treatment in 30, 60 or 90 days.

    Trial name
    NCT07601074
    Testing
    Lopinavir / ritonavir
    Where
    8 sites in United States
    Volunteers
    118 people
    Sponsor
    Daré Bioscience, Inc.
    Can I take part? NCT07601074
  • HIV-1-infection

    A Study to Provide Continued Access to Study Drug to Children and Adolescents Who Have Completed Clinical Studies Involving Gilead HIV Treatments

    • Recruiting
    • Age: 1 month and older
    • Phase 4
    • Pill or oral medicine

    The goal of this clinical study is to provide continued access to the study drug(s) to children and adolescents with human immunodeficiency virus type 1 (HIV-1) who completed their participation in an applicable parent study and…

    Trial name
    NCT06337032
    Testing
    F/TAF (High Dose Tablet), F/TAF (Low Dose Tablet), F/TAF (Lowest Dose Tablet)
    Where
    15 sites in Argentina, Panama and 4 more
    Volunteers
    350 people
    Sponsor
    Gilead Sciences
    Can I take part? NCT06337032
  • COVID-19, Immunodeficiency

    OPtimisation of Antiviral Therapy in Immunocompromised COVID-19 Patients: a Randomized Factorial Controlled Strategy Trial

    • Recruiting
    • Age: 16 years and older
    • Phase 2

    The overall purpose of the trial is to evaluate the efficacy and safety of possible combination antiviral therapy DAA (remdesivir + nirmatrelvir/r)∞ versus the reference monotherapy (nirmatrelvir/r alone) and to assess the…

    Trial name
    OPTICOV (NCT05587894)
    Testing
    Paxlovid 5 days, Paxlovid 10 days, Veklury
    Where
    18 sites in France, Italy and 1 more
    Volunteers
    256 people
    Sponsor
    ANRS, Emerging Infectious Diseases
    Can I take part? OPTICOV
  • COVID-19, SARS-CoV-2 Infection, RSV

    Clinical Outcomes and Pharmacotherapy Effectiveness in the VA Health Care System (COPE-VA)

    • Recruiting
    • Age: 18 years and older
    • Observational study

    The purpose of this study is to comprehensively describe the temporal and geographic utilization of COVID-19 therapies used for mild to moderate disease during different periods of SARS-CoV-2 variant circulation as well as to…

    Conditions
    COVID-19, SARS-CoV-2 Infection, RSV, Influenza
    Trial name
    COPE-VA (NCT06160128)
    Where
    United States
    Volunteers
    400,000 people, healthy volunteers welcome
    Sponsor
    VA Office of Research and Development
    Can I take part? COPE-VA
  • HIV Infection

    Very Early Intensive Treatment of Infants Living With HIV to Achieve HIV Remission

    • Recruiting
    • Age: Up to 48 hours
    • Phase 1/2

    The study will explore the effects of early intensive antiretroviral therapy (ART) with or without a broadly neutralizing antibody (bNAb) on achieving HIV remission (HIV RNA below the limit of detection of the assay) among…

    Trial name
    NCT02140255
    Testing
    Nucleoside Reverse Transcriptase Inhibitors (NRTIs), Nevirapine (NVP), Lopinavir/Ritonavir (LPV/r)
    Where
    47 sites in United States, Argentina and 11 more
    Volunteers
    1,120 people
    Sponsor
    National Institute of Allergy and Infectious Diseases (NIAID)
  • HIV Infection

    An Adaptive Platform Trial for Evaluation of Novel Treatment Regimens in Children and Adolescents With HIV in Africa

    • Not yet recruiting
    • Age: 4 weeks to 14 years
    • Phase 3

    The goal of the CHAPAS-5 clinical trial is to find out how well different HIV treatments work in children and young people (from 4 weeks up to under 15 years old) living with HIV, including those starting treatment for the first…

    Trial name
    CHAPAS-5 (NCT07792096)
    Testing
    Dolutegravir (DTG), Abacavir (ABC), Lamivudine (3TC)
    Volunteers
    800 people
    Sponsor
    University College, London
    Can I take part? CHAPAS-5
  • HER2-positive Advanced Solid Tumor

    A Phase 1/2a Study of DB-1303/BNT323 in Advanced/Metastatic Solid Tumors

    • Recruiting
    • Age: 18 years and older
    • Phase 1/2
    • Injection or infusion

    This is a dose-escalation and dose-expansion Phase 1/2a trial to evaluate the safety and tolerability of DB-1303/BNT323 in subjects with advanced solid tumors that express HER2.

    Trial name
    NCT05150691
    Testing
    DB-1303/BNT323, Pertuzumab Injection, Ritonavir
    Where
    102 sites in United States, Australia and 4 more
    Volunteers
    796 people
    Sponsor
    DualityBio Inc.
    Can I take part? NCT05150691
  • 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

Completed, with results posted

All 321
  • Chronic Delta Hepatitis

    Titrating-Dose of Lonafarnib in Combination With Ritonavir

    • Completed
    • Age: 18 to 65 years
    • Phase 2
    • Results posted

    A phase 2, open-label study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamic activity of titrating-dose lonafarnib/ritonavir in patients chronically infected with hepatitis delta virus (HDV)

    Trial name
    LOWR-4 (NCT02527707)
    Testing
    lonafarnib, Ritonavir
    Volunteers
    15 people
    Sponsor
    EIT Pharma, Inc.
    Can I take part? LOWR-4
  • Chronic Hepatitis D Infection

    Lonafarnib With and Without Ritonavir in HDV (LOWR-1)

    • Completed
    • Age: 18 to 65 years
    • Phase 2
    • Results posted

    To Evaluate the Safety and Efficacy of Lonafarnib with and without Ritonavir Boosting in Adults With Genotype 1 Chronic Hepatitis D Virus (HDV) Infection (LOWR-1).

    Trial name
    LOWR-1 (NCT02430181)
    Testing
    lonafarnib, peginterferon alfa-2a, ritonavir
    Where
    Turkey (Türkiye)
    Volunteers
    21 people
    Sponsor
    EIT Pharma, Inc.
    Can I take part? LOWR-1
  • Chronic Hepatitis D Infection

    Lonafarnib Boosted With Ritonavir With and Without Peginterferon Alfa-2a (PEG IFN-a) in HDV (LOWR-2)

    • Completed
    • Age: 18 to 65 years
    • Phase 2
    • Results posted

    An Open-label, Dose-ranging Study to Evaluate the Safety and Efficacy of Lonafarnib with Ritonavir Boosting +/- Peginterferon alfa-2a in Patients Chronically Infected with Delta Hepatitis (HDV) (LOWR-2).

    Trial name
    LOWR-2 (NCT02430194)
    Testing
    lonafarnib, ritonavir, Pegylated interferon-alfa-2a
    Where
    Turkey (Türkiye)
    Volunteers
    55 people
    Sponsor
    EIT Pharma, Inc.
    Can I take part? LOWR-2
  • Human Immunodeficiency Virus, Treatment

    First in Human Study of TLC-ART 101 (ACTU 2001)

    • Completed
    • Age: 18 to 65 years
    • Phase 1
    • Results posted

    This study is a prospective, open-label, single-site, first-in-human study of a long-acting, injectable combination antiretroviral therapy platform, with a pharmacologically-guided adaptive design for dose escalation…

    Conditions
    Human Immunodeficiency Virus, Treatment, Antiretroviral Therapy
    Trial name
    NCT05850728
    Testing
    TLC-ART
    Where
    United States
    Volunteers
    12 people, healthy volunteers welcome
    Sponsor
    University of Washington
    Can I take part? NCT05850728
  • Healthy Participants

    A Study to Learn About the Medicine (PF-07321332 or Nirmatrelvir/Ritonavir) in Healthy Lactating Women

    • Completed
    • Age: 18 to 55 years
    • Phase 1
    • Results posted

    The main purpose of this study is to measure the level of active ingredient of the study medicine (nirmatrelvir) that is secreted in human breast milk when it is given to healthy breastfeeding women.

    Trial name
    NCT05441215
    Testing
    nirmatrelvir, ritonavir
    Where
    Belgium
    Volunteers
    8 people, healthy volunteers welcome
    Sponsor
    Pfizer

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