NAD+
/N · A · D plus/aka Nicotinamide adenine dinucleotide, NAD, Beta-NAD
A coenzyme, not a peptide, that every cell needs for energy metabolism and DNA repair, and whose levels appear to fall with age in some tissues.
NAD+: educational research discussion. Not medical advice. Not a protocol for you.Details
- Reported range
- 250–2,000 mg (oral precursors)
- Frequency
- Daily (oral)
- Cycle length
- Continuous; trials ran 6–12 weeks
- Half-life
- Not meaningful; rapid turnover
- Route
- Oral, SC or IV (clinic)
Reported figures describe what is published or discussed. None of them is a dose for you.
Mechanism
What it is proposed to do
NAD+ carries electrons in energy metabolism and is consumed by sirtuins, PARPs (DNA repair enzymes) and CD38. In animals, falling NAD+ tracks with ageing, and raising it improves some age-related measures in mice. Cells mostly build NAD+ from precursors: oral NMN and NR are converted inside cells. Extracellular NAD+ is generally thought to be broken down to smaller precursors before cells take it up, so how much infused NAD+ reaches tissues intact is unclear. In a 6-hour IV study, plasma NAD+ did not rise at all for the first 2 hours.
- 01
NAD+ or precursor
Oral NMN or NR, or SC/IV NAD+
established - 02
Cellular NAD+ pool
Oral precursors raise blood NAD+ in human RCTs
established - 03
Sirtuins · PARPs · mitochondria
NAD+-dependent enzymes; benefit from boosting shown mainly in animals
proposed - 04
Healthier ageing
Human outcome effects small or mixed so far
proposed
Half-life. Not a useful single number. Infused NAD+ is taken up and metabolized so fast that plasma levels did not rise for the first 2 hours of a 6-hour infusion. Oral precursor trials dose daily for weeks.
Dosing & cycles
What is reported, and where it comes from
Numbers below are labeled FDA label, clinical trial range or commonly reported range. They describe the published and discussed landscape. They are not instructions and not a protocol for you.
Dosing studio
Every figure is labeled by where it comes from.
Scale view: NMN trial dose
Probe at 250 mg: at the listed figure Drag it to read the scale. It does not pick a number for you.
Typical cycle, as a calendar
Trial pattern: daily oral precursor
6–12 weeks in trials
Precursor trials give a fixed daily dose for weeks and measure blood NAD+ and metabolic markers. None ran long enough to test ageing outcomes.
Cycle patterns
Trial pattern: daily oral precursor
Precursor trials give a fixed daily dose for weeks and measure blood NAD+ and metabolic markers. None ran long enough to test ageing outcomes.
Community pattern: SC 2× weekly
A common injection rhythm in clinic protocols. The spacing is convention; no study compares schedules.
Stacks
What it gets combined with
Why people pair things, and what nobody has tested.
NAD+ + longevity peptides
3 compounds- Why people combine these
- Pitched as one protocol covering NAD, mitochondria (MOTS-c) and telomeres (epitalon).
- Caution
- Each piece has thin human outcome data. Combining them makes it impossible to tell what, if anything, did something.
- What is unknown
- No published human data on this combination: dosing, interactions and long-term effects are all unstudied.
NAD+ + 5-amino-1MQ
2 compounds- Why people combine these
- 5-amino-1MQ inhibits NNMT, an enzyme that uses up nicotinamide, an NAD+ building block. The pitch is that it spares the NAD pool.
- Caution
- Mouse-level reasoning. We found no published human trials of 5-amino-1MQ.
- What is unknown
- No published human data on this combination: dosing, interactions and long-term effects are all unstudied.
Evidence
How much of this is known
Evidence grade
C
Thin human data
Human data thin (pilots, uncontrolled, or none completed). Strong animal data and a lot of anecdote.
How we gradeGraded C overall. Evidence that oral precursors raise NAD+ is solid; evidence for health outcomes is modest, and injected or IV NAD+ rests on pilot data.
Human trial status
Oral NR at 1,000 mg/day raised NAD+ in blood cells by about 60% in a 2018 crossover trial of 24 adults aged 55–79, with blood pressure trends that did not reach significance. NR at 2,000 mg/day for 12 weeks did not improve insulin sensitivity in 40 obese men. NMN at 250 mg/day for 10 weeks improved muscle insulin sensitivity in 25 prediabetic women (2021). For IV NAD+, the main published data are a 2019 metabolism pilot in 8 men and small uncontrolled clinic reports.
Limitations
- Raising a blood NAD+ number is not the same as a health benefit.
- Precursor trials are small and short (6–12 weeks).
- IV and SC NAD+ lack controlled trials for any outcome.
- Much of the ageing rationale comes from mouse studies.
Sources to read
- Martens CR et al. Chronic nicotinamide riboside supplementation is well-tolerated and elevates NAD+ in healthy middle-aged and older adults (Nat Commun 2018)
- Dollerup OL et al. A randomized placebo-controlled clinical trial of nicotinamide riboside in obese men (Am J Clin Nutr 2018)
- Yoshino M et al. Nicotinamide mononucleotide increases muscle insulin sensitivity in prediabetic women (Science 2021)
- Grant R et al. A pilot study investigating changes in the human plasma and urine NAD+ metabolome during a 6 hour intravenous infusion of NAD+ (Front Aging Neurosci 2019)
- Intravenous NAD+ versus nicotinamide riboside: a retrospective tolerability pilot study in a real-world setting (Front Aging 2026)
Links open PubMed, DailyMed, FDA or trial-registry searches. We do not cite what we have not described accurately.
Safety
Side effects, cautions, status
Commonly reported effects
- IV infusions: flushing, chest tightness or pressure, nausea, abdominal cramping and a racing heart are commonly reported, mainly at fast infusion rates.
- In one small 2026 retrospective clinic report, all six people given 500 mg IV NAD+ reported symptoms such as cramping, nausea, chest pressure or raised heart rate.
- Oral NR and NMN were well tolerated in trials of up to 12 weeks, including 2,000 mg/day of NR. Mild GI upset is occasionally reported.
- Long-term effects of chronically raising NAD+ are unknown. Tumors also use NAD+, a theoretical concern with no human data either way.
Who should be extra cautious
- Active cancer. Tumor cells depend on NAD+ too. Whether raising it matters is unknown; the concern is theoretical.
- Heart conditions. Chest pressure and raised heart rate are reported during fast IV infusions.
- Pregnancy or breastfeeding. Not studied for precursor supplements at trial doses or for injected NAD+.
- Tested athletes. IV volumes over 100 mL per 12 hours are prohibited outside hospital settings (WADA M2.2).
- Clinic IV drips. Product quality, sterility and medical oversight vary by provider.
Legal & regulatory status
Not an FDA-approved drug in any form. Oral NR is sold as a dietary supplement, and in late September 2025 FDA declared NMN lawful in dietary supplements, reversing its 2022 position. Injectable and IV NAD+ are offered by wellness and IV clinics without an approved indication.
WADA. NAD+ itself is not named on the Prohibited List. The delivery method can be the violation: IV infusions or injections of more than 100 mL per 12 hours are prohibited (M2.2) except in hospital treatment, surgical procedures or clinical investigations, and many clinic drips exceed that volume. Confirm with your federation.
Storage & handling, high level
Oral precursors are shelf-stable supplements, and supplement content is not FDA-reviewed before sale. Injectable NAD+ is sensitive to heat and light. Sterility and product quality matter more than any number on this page.
Reconstitution and injection technique are clinical skills. The reconstitution calculator does arithmetic only.
FAQ
Questions people ask about NAD+
Is NAD+ a peptide?
NAD+, NMN or NR: what is the difference?
Do IV NAD+ drips work?
Why do fast drips cause chest tightness?
Is NMN legal to sell as a supplement?
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