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

31.10.2017

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.

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