© 2019 IPHARMA

  • Facebook Social Icon
  • LinkedIn Social Icon
  • YouTube Social  Icon
  • Instagram Social Icon

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

09.06.2017

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

Please reload

Недавние посты
Please reload

Архив
Please reload