Статус: | Terminated |
Фаза: | Phase 2 |
Начало: | 10 марта 2015 г. |
Окончание: | 31 марта 2017 г. |
Описание: | The objective of the study is to evaluate the efficacy and safety of Reparixin treatment (2.772 mg/kg body weight/hour intravenous continuous infusion for 7 days) based on incidence of early allograft dysfunction within the first 7 days after orthotopic liver transplantation (OLT) and overall indicators of allograft dysfunction in the early postoperative period (within 14 days after the OLT). |
смотреть на ClinicalTrials.gov |
Статус: | Terminated |
Фаза: | Phase 2 |
Начало: | 10 марта 2015 г. |
Окончание: | 31 марта 2017 г. |
Описание: | The objective of the study is to evaluate the efficacy and safety of Reparixin treatment (2.772 mg/kg body weight/hour intravenous continuous infusion for 7 days) based on incidence of early allograft dysfunction within the first 7 days after orthotopic liver transplantation (OLT) and overall indicators of allograft dysfunction in the early postoperative period (within 14 days after the OLT). |
смотреть на ClinicalTrials.gov |