PROMPT - Palifermin in Reduction of Oral Mucositis in PBSC Transplantation

Status Completed

Clinical Trial Summary

This is an open-label, single-arm, multicentre study conducted in Spain to estimate the effectiveness of palifermin administered at a dose of 60 mg/kg/day IV for 3 consecutive days before the start of the conditioning regimen and for 3 consecutive days after autologous PBSCT for treating oral mucositis in patients with NHL and MM who have received high-dose conditioning chemotherapy.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00352703
Study type	Interventional
Source	Swedish Orphan Biovitrum
Contact
Status	Completed
Phase	Phase 4
Start date	April 2006
Completion date	May 2007

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