Clinical trial

A Study to Investigate the Neuroprotective Effect of PROCRIT (Epoetin Alfa)…

NCT00267007 · Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry · Terminated

Key facts

NCT number NCT00267007
Title A Study to Investigate the Neuroprotective Effect of PROCRIT (Epoetin Alfa) Versus Placebo in Cancer Patients Who Develop Chemotherapy-induced Peripheral Neuropathy
Official title A Randomized, Double-Blind, Placebo-Controlled, Multicenter, 18 Week Pilot Study to Investigate the Neuroprotective Effect of PROCRIT (Epoetin Alfa) on the Development of Peripheral Neuropathy in Patients Receiving Combination Taxane and Platinum-Based Chemotherapy for Cancer
Lead sponsor Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry
Collaborators Ortho Biotech Clinical Affairs, L.L.C. Industry
Status Terminated
Phase Phase 2
Study type Interventional
Conditions Peripheral Neuropathy, Chemotherapy-induced
Intervention type Drug
Interventions PROCRIT 40, 000 IU QW, Placebo
Enrollment 32
Start date Jun 1, 2006
Primary completion Aug 1, 2008
Completion Aug 1, 2008
First posted Dec 20, 2005
Last update posted Jun 4, 2014
Countries United States

At a glance

  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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