- 26 авг. 2016 г.
IPHARMA was authorized to conduct the Phase I clinical trial of medicinal product ИД 4025
In August 2016, IPHARMA LLC was authorized by the Ministry of Healthcare of the Russian Federation to conduct the Phase I clinical trial of medicinal product ИД-4025. Protocol № HCV-ИД4025-04 "Double-blind randomized placebo-controlled study to evaluate the safety, tolerability and pharmacokinetics of rising doses of ИД-4025 for single oral use in healthy subjects". Study Objective: to evaluate the safety and tolerability of ИД-4025 for single use in healthy subjects. The are
- 26 авг. 2016 г.
ИФАРМА получила разрешение Минздрава на проведение исследования I фазы препарата ИД-4025
В августе 2016 г. ИФАРМА получила разрешение Министерства здравоохранения РФ на проведение клинического исследования I фазы препарата ИД-4025. Протокол № HCV-ИД4025-04 «Двойное-слепое рандомизированное плацебо-контролируемое исследование безопасности, переносимости и фармакокинетики возрастающих доз препарата ИД-4025 при однократном пероральном применении у здоровых добровольцев«». Цель клинического исследования: оценка профиля безопасности и переносимости препарата ИД-4025 п
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