On 25th of April, 2016, IPHARMA was authorized by the Ministry of Healthcare of the Russian Federation to conduct the Phase I clinical trial of the medicinal product XC125.

Protocol № ARI-XC125-01 «Double-blind randomized placebo-controlled clinical study of safety, tolerability, pharmacokinetics and pharmacodynamics of rising doses of XC125 for single and multiple oral use in healthy subjects».

The purpose of this clinical trial is to study safety, tolerability, pharmacokinetics and pharmacodynamics of rising doses of the study drug.

The area of the study drug XC125 use – infectious diseases.

IPHARMA has a large experience in conducting Phase I-III studies in this therapeutic area. The company specialists will manage monitoring, data collecting and processing, medical expertise and study report preparation in accordance with international standards.

«IPHARMA» LLC – an accredited partner of the «Skolkovo» Technopark, Contract Research Organization (CRO), specialized in conducting clinical trials of innovative medicinal products of Russian and foreign developers.

The main competence of the company is the effective and rational organization of clinical trials according to international standards as well as the drug registration support in Russia. IPHARMA team consists of the qualified specialists with an extensive experience in international and local clinical trials. The company has a large scientific background, its own medical expertise and an ability to involve top Russian and foreign specialists.


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