Ignite Creation Date:
2024-05-05 @ 11:36 AM
Last Modification Date:
2024-10-26 @ 9:10 AM
Study NCT ID:
NCT00094861
Status:
COMPLETED
Last Update Posted:
2017-03-14
First Post:
2004-10-27
Brief Title:
Study to Evaluate Palifermin in the Reduction of Dysphagia in Patients With Locally Advanced Non-Small Cell Lung Cancer NSCLC
Sponsor:
Swedish Orphan Biovitrum
Organization:
Swedish Orphan Biovitrum
Study Overview
Official Title:
A Phase 2 Study to Evaluate the Efficacy and Safety of Palifermin Recombinant Human Keratinocyte Growth Factor in the Reduction of Dysphagia in Patients Receiving Concurrent Chemoradiotherapy Followed by Consolidation Chemotherapy for Locally Advanced Non-Small Cell Lung Cancer NSCLC
Status:
COMPLETED
Status Verified Date:
2017-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to determine if palifermin will reduce the incidence of dysphagia in patients receiving concurrent chemoradiotherapy followed by consolidation chemotherapy for treatment of unresectable stage III Non-Small Cell Lung Cancer NSCLC
Detailed Description:
During the acute dysphagia evaluation phase the period lasting from the administration of the first dose of investigational product through Week 12 or up to Week 16 if dysphagia is not resolved to CTCAE v30 grade 1 by Week 12 participants underwent acute dysphagia assessments twice weekly All participants were followed for disease progression second primary tumors other malignancies and overall survival until death or loss to follow-up during the long term follow-up still ongoing
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None