Meta Information
ID:nad
Name:NAD+ (IV Therapy)
Schema Version:1.5
Alternate Names
- Nicotinamide Adenine Dinucleotide IV
- IV NAD+ Therapy
Active Compound
Nicotinamide adenine dinucleotide
Intervention Type
therapeutic_agent
Delivery
Route:
intravenous
Scope:
- systemic
Regulatory Status
- us:unregulated_compounded_agent
Indication
Focus:
healthspan
Description:
Aims to restore cellular levels of NAD+, a critical coenzyme for metabolism and DNA repair, to combat age-related decline.
Typical Protocol
- Initial loading phase of 500-1000mg infusions over several days, followed by monthly or quarterly maintenance infusions.
Expected Cost Mean
Low Cost:
500
High Cost:
1500
Cost Type:
procedure
Description:
Per-infusion cost at private clinics; not covered by insurance.
Summary
NAD+ is a vital coenzyme essential for cellular energy production and the function of sirtuins, proteins involved in DNA repair and stress resistance. NAD+ levels decline significantly with age, and this decline is linked to many age-related dysfunctions. Intravenous administration bypasses metabolic breakdown, delivering the molecule directly to the bloodstream with the goal of restoring youthful cellular function.
Purpose
Replenishes a key cellular coenzyme for energy and repair.
Card Summary
Intravenous infusion to restore declining levels of NAD+, a vital coenzyme for cellular energy metabolism and DNA repair, potentially mitigating age-related dysfunction.
Drug Class
null
Drugs In Class
Empty Array
Impact
Score:
2.5
Justification:
Strong biological rationale but lacks robust human RCTs for healthspan outcomes.
Evidence
Grade:
C
Score:
3
Justification:
Primarily based on animal models and mechanistic data; lacks large-scale human trials.
Safety
Score:
5.5
Justification:
Requires medical supervision; common infusion-related side effects and limited long-term safety data.
Flags
- Infusions can cause significant discomfort including nausea, flushing, cramping, and headache.
- Long-term effects of supra-physiological NAD+ levels in healthy humans are unknown.
- Efficacy for extending human healthspan is currently unproven in clinical trials.
- Administered in private clinics, often with variable quality control and oversight.
Verdict
Theoretically promising but expensive and unproven for human healthspan benefits.
Qualifier
route: IV, scope: systemic, focused on healthspan
Created
2026-05-05T22:21:59.129169Z
Ai Model
Gemini 2.5 Pro (High)