drugset / Trial / NCT00406016

Acute Safety, Tolerability, Feasibility and Pharmacokinetics of Intrath. Administered ATI355 in Patients With Acute SCI

NCT00406016 ↗

Phase 1 Completed 52 enrolled Novartis
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate the acute safety, tolerability, feasibility and pharmacokinetics of 6 dose regimens of ATI355 in acute spinal cord injury patients

Timeline

Start
2006-05
Primary completion
2011-09
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject ATI355 Unknown — Intrathecal

Indications