With so many scientific reports on animals, Effepharm decided to conduct our own clinical study on Uthever™.
Our clinical study would start from:
(1) Safety assessment
(3) Boosting energy and increasing endurance
The clinical study on UtheverTM is registered in the US and WHO’s official clinical registry system and displayed on the websites to the public.
Title: Evaluate the Efficacy and Safety of Uthever NMN(Nicotinamide Mononucleotide, a Form of Vitamin B3)
Official Title: A Multicentre, Randomized, Double Blind, Parallel Design, Placebo Controlled Study to Evaluate the Efficacy and Safety of UtheverTM (NMN), an Orally Administered Supplementation in Middle Aged and Older Adults.
US register ID: NCT04228640
Study Type: Interventional (Clinical Trial)
Estimated Enrollment: 66 participants
Intervention Model: Parallel Assignment
Intervention Model Description: A Multicenter, Randomized, Double-Blind, Placebo-Controlled
Primary Purpose: Prevention
To assess its safety, physical examination, blood biochemistry test, BMI, HOMA will be performed at baseline and end of the study. Blood cellular NAD+ and NADH concentration in serum will de determined to confirm its ability to increase NAD level in human body.
Effepharm is proud to be the first and the only NMN manufacturer in the world to conduct clinical trials. The clinical study on UtheverTM is the largest scale in the world according to WHO’s clinical database.