Overview

Efficacy and Safety of LFG316 in Transplant Associated Microangiopathy (TAM) Patients

Status:
Terminated
Trial end date:
2017-06-30
Target enrollment:
Participant gender:
Summary
This was a randomized, SoC-controlled, open-label, multi-center study in patients with TAM after hematopoietic precursor cell transplantation (HPCT) . Study consisted of up to 28 days of screening period, 16 weeks treatment period that can be extended to 45 weeks.Approximately 40 patients was to be randomized to receive SoC or LFG316 plus SoC. Patients was included in the study if they have diagnosis of TAM and poor prognostic markers. This trial was terminated: LFG316, a monoclonal antibody inhibitor of complement factor 5 (C5), had been studied in seven patients with transplantation-associated microangiopathy (TAM). Due to low confidence of clinical benefit, this study was closed
Phase:
Phase 2
Details
Lead Sponsor:
Novartis Pharmaceuticals