10 Participants NeededMy employer runs this trial

Nicotinamide Riboside for Pulmonary Hypertension

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Overseen ByThomas E Strayer, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Vanderbilt University Medical Center

What You Need to Know Before You Apply

What is the purpose of this trial?

Pulmonary hypertension (PH) is a serious condition that puts strain on the heart and lungs and often leads to frequent hospital stays and shortened life expectancy. The most common cause is heart disease affecting the left side of the heart. A particularly high-risk form, called combined pre- and post-capillary pulmonary hypertension (CPH), occurs in about one in four people with heart failure. There are currently no approved treatments for CPH, and many patients develop right-sided heart failure and die earlier than expected.

This study is based on a new approach that uses advanced computer methods to analyze a patient's unique biology and identify potential drug targets. Using this method, we identified nicotinamide riboside (NR) as a promising option for people with CPH. NR is a form of vitamin B3 that helps the body make NAD⁺, a substance essential for how cells produce energy and stay healthy. NAD⁺ plays an important role in how heart and blood vessel cells function.

Previous research in animals suggests NR may help improve blood vessel changes in the lungs and support heart function. NR has also shown potential benefits in human studies related to cell energy, mitochondrial health, and reducing oxidative stress. In this study, NR is used only as a dietary supplement that supports normal body processes, not as a proven treatment.

The investigators will conduct a small, carefully controlled study in which participants receive NR and a placebo at different times. The goal is to understand how NR affects biological and biochemical markers in the body, not to test whether it improves symptoms or outcomes. Any clinical measurements are included only to help interpret the biological effects.

Who Is on the Research Team?

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Evan L Brittain, MD

Principal Investigator

VUMC

Are You a Good Fit for This Trial?

Inclusion Criteria

I am able to walk on my own and complete a walking test.
I am between 18 and 85 years old.
A qualifying Baseline RHC performed within 2 years of consent Clinical echocardiogram within the prior year with LVEF>/= 45%
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Exclusion Criteria

I have PAH caused by drugs or toxins and am currently using those substances.
I have pulmonary hypertension caused by a heart defect, connective tissue disease, or inherited condition.
My lung function is below 60% and I have moderate or worse lung imaging issues.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive nicotinamide riboside (NR) and placebo at different times to study the effects on biological and biochemical markers

15 weeks
Visits at Baseline, Week 6, Week 9, Week 15

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Nicotinamide Riboside (NR)

How Is the Trial Designed?

2

Treatment groups

Active Control

Placebo Group

Group I: Nicotinamide riboside (NR)Active Control1 Intervention
Group II: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Vanderbilt University Medical Center

Lead Sponsor

Trials
922
Recruited
939,000+

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator

Trials
3,987
Recruited
47,860,000+