© 2019 IPHARMA

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IPHARMA had received the Ministry of Health permission to conduct Phase I study of Testonorm®


On June 7, 2017, IPHARMA had received the Ministry of Health of the Russian Federation permission to conduct a Phase I clinical trial of Testonorm®.


Protocol No. ANDR-TSN-01 "Double-blind, randomized, placebo-controlled study of the safety and tolerability of increasing doses of Testonorm® with single and subsequent multiple intramuscular injection in healthy volunteers."


The purpose of the clinical study: evaluate the safety profile and tolerability of the drug Testonorm® for a single and subsequent repeated administration to healthy volunteers.


Therapeutic area: urology.


 The leading organization in the study is I.M.Sechenov First Moscow State Medical University

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