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CompletedNCT01935154

Efficacy Study of Vx001 Vaccine in NSCLC Patients

Phase II Study of Vx001 Vaccine in HLA-A*0201 Positive Patients With TERT Positive Stage IV or Recurrent Stage I-III NSCLC

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
221 (actual)
Sponsor
Vaxon Biotech · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Patients with stage IV or recurrent stage I-III NSCLC with documented disease control (objective response or stable disease) within 3 weeks after platinum based 1st line chemotherapy; only HLA-A\*0201 positive patients with TERT expressing tumors will be included. The objective of the trial is survival rate at 12 months.

Conditions

Interventions

TypeNameDescription
DRUGVx-001
DRUGPlacebo

Timeline

Start date
2012-08-01
Primary completion
2017-01-01
Completion
2017-01-01
First posted
2013-09-04
Last updated
2019-06-19

Locations

70 sites across 8 countries: Czechia, France, Germany, Greece, Italy, Poland, Romania, Spain

Source: ClinicalTrials.gov record NCT01935154. Inclusion in this directory is not an endorsement.

Efficacy Study of Vx001 Vaccine in NSCLC Patients (NCT01935154) · Clinical Trials Directory