drugset / Trial / NCT01966666

A Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy Study of TPI-287 in Alzheimer's Disease

NCT01966666

Phase 1 Completed 29 enrolled University of California, San Francisco
RandomizedParallel-groupQuadruple-blindOther

Summary

The purpose of the study is to determine the highest dose of TPI-287 that is safe and tolerable when administered as an intravenous infusion to participants with mild to moderate Alzheimer's disease (AD), to measure pharmacokinetic properties of the drug as well as to gauge preliminary efficacy of TPI-287 on disease progression.

Timeline

Start
2013-11
Primary completion
2019-09
Completion
2019-09

Drugs

EvaluationDrugModalityDoseRoute
Subject TPI 287 Small molecule 2 mg/m2 Intravenous
Subject TPI 287 Small molecule 6.3 mg/m2 Intravenous
Subject TPI 287 Small molecule 20 mg/m2 Intravenous

Indications