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Study identifier: NCT05284617 Synced from ClinicalTrials.gov · July 28, 2026
● Completed

Exploratory Ph 2A, Double-Blind, Placebo-Controlled Dose Escalation Study of Safety, Tolerability, PD, & PK of HU6 for Subjects With Obese HFpEF

Condition: Heart Failure With Preserved Ejection Fraction  ·  Sponsor: Rivus Pharmaceuticals, Inc.

PhasePhase 2
Planned participants67
Who can joinAll sexes, 40 Years to no upper limit
Healthy volunteersNo

About this study

This is a Phase 2A, randomized, parallel-group, placebo-controlled, double-blind, within subject dose escalation trial with 3 dose levels of HU6 and placebo. Subjects will be randomized (1:1) either to HU6 or placebo. Two dose levels will be administered in sequential order (150 mg daily followed by 300 mg daily), each for 20 days, to reach the third and highest dose of 450 mg daily if safety and tolerability are demonstrated at the lower 2 preceding doses. Administration of the 450 mg high dose will continue for a total of 94 days, with a safety follow-up visit within \~14 days of the last dose.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (15)

National Heart InstituteBeverly Hills, California, United States
Lundquist Institute for Biomedical Innovation at Harbor UCLA Medical CenterTorrance, California, United States
New Generation of Medical ResearchHialeah, Florida, United States
Broward Research CenterPembroke Pines, Florida, United States
Northwestern UniversityChicago, Illinois, United States
The University of Chicago Medical CenterChicago, Illinois, United States
Johns Hopkins UniversityBaltimore, Maryland, United States
Massachusetts General HospitalBoston, Massachusetts, United States
Mayo ClinicRochester, Minnesota, United States
Saint Luke's Mid America Heart InstituteKansas City, Missouri, United States
Weill Cornell MedicineNew York, New York, United States
Wake ForestWinston-Salem, North Carolina, United States

+ 3 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05284617