跳至主要内容
临床试验/NCT05517122
NCT05517122已完成不适用

Effect of Oral NAD+ Precursors Administration on Blood NAD+ Concentration in Healthy Adults

Société des Produits Nestlé (SPN)2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2022年7月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
68
试验地点
2
主要终点
Compare the extent of increase in NAD+ level in whole blood across the 3 NAD+ precursors (NAM, NR and NMN)

研究概览

简要总结

Nicotinamide adenine dinucleotide (NAD) is a coenzyme playing a central role in human metabolic pathways. A recognized approach to increase NAD level is through oral supplementation of its precursors promoting NAD synthesis in vivo. NAD precursors exist in multiple forms. However, it is unclear how the various precursors compare in their ability to increase NAD levels in human blood. The purpose of this study is to compare the effect of 3 NAD precursors on whole blood NAD metabolome.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy male and female aged 18-50 years, inclusive, at enrolment
  • Body mass index (BMI) between 18.5 to 27.0 kg/m².
  • Able to understand and to sign a written informed consent prior to study enrolment.
  • Willing and able to comply with the requirements for participation in this study.

排除标准

  • Known history of allergy or intolerance to the investigational products.
  • Any chronic medical condition and/or history of significant medical condition, which in the opinion of the site physician/ investigator may risk participant wellbeing/ safety, impede participant compliance with study procedures or ability to complete the study and/ or could confound the primary objectives of the study.
  • Any acute illness or any recent medical intervention including vaccination within 14 days before the first dose of investigational product.
  • Female participants who are pregnant or intending to become pregnant, lactating and/or breastfeeding. Women of childbearing potential who are not currently using medically effective forms of contraception.
  • Use of prescription drugs known to potentially interact with NAD precursors within 14 days or 5 half-lives (whichever is longer) prior to the first dose of investigational product.
  • Use of multivitamin/ multimineral supplements, NAD+ precursor supplementation (e.g., niacin, nicotinic acid or niacinamide), L-tryptophan supplementation and/ or any over-the- counter (OTC) medication promoting "healthy aging" or "anti-aging" or "longevity" up to 30 days before first dose of investigational product.
  • On a self-restricted diet, controlled diet or special therapeutic diet up to 30 days before first dose of investigational product.
  • Average alcohol consumption greater than 2 standard drinks per day over a week for males, and greater than 1 standard drink per day over a week for females. One standard drink contains 10-12 g of ethanol. Examples of standard drinks are one beer can (300 ml), one glass of wine (100 ml) or one glass of schnaps (30 ml).
  • Current smoker (e.g., cigarette, tobacco, cannabis) who exceeds 5 cigarettes per week.
  • Performing shift work or trans-meridian travel greater than two time zones within 14 days prior to the first dose of investigational product.
  • Currently participating in another research study.
  • Family or hierarchical relationships with the Clinical Innovation Lab (CIL) team.

结局指标

主要结局

Compare the extent of increase in NAD+ level in whole blood across the 3 NAD+ precursors (NAM, NR and NMN)

时间窗: at Day 14

Measure the changes in whole blood NAD+ level across interventions: NAM vs NR, NAM vs NMN, NR vs NMN by quantitative liquid chromatography-mass spectroscopy

Determine the extent of increase in NAD+ level in whole blood, for each NAD+ precursor (NAM, NR and NMN) compared to placebo

时间窗: at Day 14

Measure the changes in whole blood NAD+ level interventions vs placebo: NAM vs placebo, NR vs placebo, NMN versus placebo by quantitative liquid chromatography-mass spectroscopy

次要结局

  • Determine the extent the NAD+ precursors(NAM, NR and NMN) affect the NAD metabolome in whole blood compared to placebo(over 4 hours at Day 1 and at Day 14.)
  • Compare the extent the NAD+ precursors (NAM, NR and NMN) affect the NAD+ metabolome in whole blood.(over 4 hours at Day 1 and at Day 14.)

研究者

发起方
Société des Produits Nestlé (SPN)
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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