drugset / Trial / NCT03423342
Nicotinamide Riboside in Systolic Heart Failure
Phase 1/2
Completed
30 enrolled
University of Washington
National Heart, Lung, and Blood Institute (NHLBI) · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Nicotinamide riboside | Small molecule | 1000 mg | Oral |