A Clinical Trial to Evaluate the Effect of Ulonivirine (MK-8507) on Heart Rhythm in Healthy Adults (MK-8507-012)
NCT07305831 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 62
Last updated 2026-04-21
Summary
Researchers are looking for new treatments for HIV-1 (human immunodeficiency virus type 1) that are safe, well-tolerated, and can be taken less often. HIV-1 is the most common type of HIV, which is a virus that attacks cells of the immune system.
Ulonivirine (MK-8507) is a study medicine designed to treat HIV-1
The goal of this study is to learn if ulonivirine does not increase the QT interval (a measure of heart rhythm on an electrocardiogram) above a certain amount. Researchers also want to learn what happens to the amount of ulonivirine in a healthy person's body over time.
Conditions
- Healthy
Interventions
- DRUG
-
Ulonivirine
Oral tablet
- DRUG
-
Oral tablet
- DRUG
-
Ulonivirine Placebo
Oral tablet
- DRUG
-
Moxifloxacin Placebo
Oral tablet
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Medical Director · Merck Sharp & Dohme LLC
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-01-22
- Primary Completion
- 2026-04-09
- Completion
- 2026-04-09
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
The Phase I Clinical Trial of Booster Vaccination of Adenovirus Type-5 Vectored COVID-19 Vaccine
NCT04568811 ·Status: COMPLETED ·Phase: PHASE1
-
Post-Marketing Non-Acute Safety Study in Japan After Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) mRNA-1273 COVID-19 Vaccine in Persons at High Risk of Severe COVID-19
NCT05894590 ·Status: COMPLETED
-
Respiratory Syncytial Virus (RSV) Human Challenge Study of Molnupiravir in Healthy Participants (MK-4482-017)
NCT05559905 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Tolerability, and Pharmacokinetics of RSV Monoclonal Antibody RSM01 in Healthy Adults
NCT05118386 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Investigate the Effects of Zelicapavir (EDP-938) on QTc Interval in Healthy Adults
NCT06601192 ·Status: COMPLETED ·Phase: PHASE1
-
A Study on the Safety and Immunogenicity of Influenza, Respiratory Syncytial Virus, Human Metapneumovirus and Parainfluenza Vaccines in Adults 18 to 49 Years of Age.
NCT06850051 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of EDP-938 in Healthy Subjects
NCT03384823 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Assess the Safety, Tolerability, and Pharmacokinetics of HFB30132A Against COVID-19 in Healthy Adults
NCT04590430 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase 2 Study to Describe the Safety and Immunogenicity of Respiratory Syncytial Virus Vaccine IN006 in Healthy Participants Aged 60 Years and Older
NCT07128121 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Experimental Vaccine for Prevention of Ebola Virus Infection
NCT00374309 ·Status: COMPLETED ·Phase: PHASE1
-
Pre-Approval Access to JNJ-53718678 for the Treatment of Respiratory Syncytial Virus (RSV) Infection in (a) Immunocompromised Adult and Pediatric Participants
NCT04221412 ·Status: NO_LONGER_AVAILABLE
-
Study on Determine the Utilisation and Clinical Outcomes of Evusheld in COVID-19 PrEP in China
NCT05917951 ·Status: COMPLETED
-
Respiratory Syncytial Virus Human Challenge in Healthy Adult Volunteers
NCT02484417 ·Status: COMPLETED ·Phase: PHASE1
-
RSV001 - A New Vaccine to Prevent Severe Viral Chest Infections.
NCT01805921 ·Status: COMPLETED ·Phase: PHASE1
-
Exploratory Clinical Study to Evaluation of the Safety and Immunogenicity of Bivalent Vaccine V-01D-351
NCT05583357 ·Status: UNKNOWN ·Phase: EARLY_PHASE1
-
Post-Marketing Safety Study in Japan in Participants With High Risk of Severe Exacerbation of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) mRNA-1273 COVID-19 Vaccine
NCT05894525 ·Status: COMPLETED
-
Study of the Safety and Immune Response of an Investigational mRNA Vaccine for the Prevention of Respiratory Syncytial Virus and/or Human Metapneumovirus in Participants Aged 18 to 49 Years and 60 Years and Older
NCT06237296 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI8897 in Healthy Adults
NCT02114268 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase 2 Study to Describe the Safety, Reactogenicity, and Immunogenicity of Herpes Zoster IN001 mRNA Vaccine (IN001) in Healthy Participants
NCT07205796 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
Safety and Immunogenicity of RNA-based Vaccines Against SARS-CoV-2 Variants in Healthy Participants
NCT05004181 ·Status: COMPLETED ·Phase: PHASE2
-
Evaluate the Safety and Immunogenicity of Ad5 COVID-19 Vaccines for Booster Use in Children Aged 6-17 Years.
NCT05330871 ·Status: UNKNOWN ·Phase: PHASE2
-
Study to Describe the Safety, Tolerability, Immunogenicity, and Efficacy of RNA Vaccine Candidates Against COVID-19 in Healthy Individuals
NCT04368728 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
A Study to Evaluate the Safety and Ability of the Vaccine to Induce Antibodies Against the Respiratory Syncytial Virus in Healthy Adults
NCT02298179 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of LY3832479 (LY-CoV016) in Healthy Participants
NCT04441931 ·Status: COMPLETED ·Phase: PHASE1
-
A Study on the Safety and Immune Response of Investigational COVID-19 mRNA Vaccines in Healthy Adults
NCT05960097 ·Status: COMPLETED ·Phase: PHASE2