drugset / Trial / NCT03423342

Nicotinamide Riboside in Systolic Heart Failure

NCT03423342

RandomizedSingle-groupTriple-blindOther

Summary

Mitochondrial dysfunction has been implicated in heart failure (HF), and is associated with an imbalance in intracellular ratio of reduced nicotinamide-adenine dinucleotide (NADH) to oxidized nicotinamide-adenine dinucleotide (NAD), or the NADH/NAD ratio. In mouse models of HF, we have found that normalization of the NADH/NAD, through supplementation with NAD+ precursors, is associated with improvement in cardiac function. This Study will randomize participants with systolic HF (ejection fraction ≤40%) to treatment with the NAD precursor, nicotinamide riboside (NR) or matching placebo, uptitrated to a final oral dose of 1000mg twice daily, to determine the safety and tolerability of NR in participants with systolic HF.

Timeline

Start
2016-05-19
Primary completion
2019-04-11
Completion
2019-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Nicotinamide riboside Small molecule 1000 mg Oral