IPHARMA received the Ministry of Health permission to conduct Phase I trial of Khondrolux®


On October, 30 IPHARMA received the Ministry of Health permission to conduct Phase I trial of Hondrolux®

Protocol № ОА-CLX-01 “Double-blind, randomized, placebo-controlled study to access safety and tolerability of single and following multiple escalating doses of the Khondrolux® study drug after a single and subsequent multiple intramuscular injection in healthy volunteers”.

The purpose of the clinical trial is to evaluate the safety and tolerability of the Khondrolux® with a single and subsequent multiple dose in healthy volunteers, including assessment of drug tolerance based on the frequency of local reactions.

Therapeutic area: rheumatology.

The Khondrolux is developed by SEA Peptides LLC for treatment and prevention of degenerative-dystrophic diseases of the joints and spine.

#phaseI

Недавние посты
Архив

© 2020 IPHARMA

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