Ignite Creation Date:
2024-05-06 @ 3:02 AM
Last Modification Date:
2024-10-26 @ 11:27 AM
Study NCT ID:
NCT02187367
Status:
TERMINATED
Last Update Posted:
2019-09-10
First Post:
2014-07-07
Brief Title:
Safety Efficacy Study of EGF Cancer Vaccine to Treat Stage IV Biomarker Positive Wild Type EGF-R NSCLC Patients
Sponsor:
Bioven Europe
Organization:
Bioven Sdn Bhd
Study Overview
Official Title:
Phase 3 Open-label Multicentre Randomised Trial to Establish Safety Efficacy of an EGF Cancer Vaccine in Inoperable Stage IV Biomarker PositiveWild Type EGF-R NSCLC Patients Eligible to Receive Standard Treatment and Supportive Care
Status:
TERMINATED
Status Verified Date:
2019-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Sponsor decision based on slow recruitment and new emerging drug combinations
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
EGF
Brief Summary:
The vaccine contains humanized recombinant antigen EGF - Epithelial Growth Factor and an adjuvant The antibodies induced by vaccination will react with circulating EGF leading to removal of EGF from the circulation As a result binding to its target EGF-Receptor is prevented Blocking of EGF-Receptor is preventing activation and stimulation of proliferation of tumour cell A Phase 3 clinical trial on the EGF vaccine is ongoing in Cuba The result from previous studies demonstrated positive correlation between extended survival and immune response against the vaccination in the late-stage NSCLC patients age below 60 with improved quality of life The purpose of this international Phase 3 trial is to determine whether the recombinant human EGF cancer vaccine is safe immunogenic and effective in the treatment of stage IV NSCLC patients who are positive in the selective EGF biomarker and wild type EGF-Receptor compared to standard treatment and supportive care
Detailed Description:
None
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
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 2013-005335-25 | EUDRACT_NUMBER | None | None |