A Pilot Phase 2 Trial of the Immunogenicity, and Safety of GI-4000; an Inactivated Recombinant S. Cerevisiae Expressing Mutant Ras Protein, as Consolidation Therapy Following Curative Treatment for Stage I-III Non-Small Cell Lung Cancer (NSCLC) With Tumor Sequence Confirmation of K-ras Mutation

GlobeImmune

Status and phase: Completed; Phase 2

Conditions: NSCLC

Treatments: Biological: GI-4000

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00655161

GI-4000-03

Details and patient eligibility

About

This is a consolidation therapy trial evaluating GI-4000 in subjects with NSCLC treated with curative intent who are disease free at their first post-treatment restaging assessment.

Full description

NSCLC is the deadliest form of human cancer, killing approximately 150,000 people a year in the United States. The best treatment for NSCLC is surgical resection. For patients with inoperable or unresectable NSCLC chemotherapy and radiation is used as first line therapy. This is a consolidation therapy trial evaluating GI-4000 in subjects with NSCLC treated with curative intent who are disease free at their first post-treatment restaging assessment. These subjects must also have a ras mutation.

Enrollment: 24 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Pathologically proven stage I-III NSCLC
• Confirmed product related ras mutation
• ECOG performance status of less than or equal to 2
• greater than or equal to 18 years of age

Exclusion criteria

• History of a previous cancer
• History of splenectomy
• History of Crohns disease or ulcerative colitis
• History of major organ transplantation
• Concurrent or chronic steroid therapy
• History of allergy to yeast
• Presence of an unstable or poorly controlled medical condition
• Pregnant or nursing mothers
• Positive skin test to yeast

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)