Antigenics is enrolling patients in a Phase II study testing the feasibility to derive an autologous investigational vaccine (HSPPC-96) from the tumor tissue of patients with resectable non-small cell lung cancer. Vaccine production will be attempted on all patients who undergo surgery and meet all inclusion/exclusion criteria.

Condition	Treatment or Intervention	Phase
Non-Small-Cell Lung Carcinoma Lung Cancer Pulmonary Cancer	Vaccine: HSPPC-96	Phase II

Further Study Details: 

Primary Outcomes: The primary goal of this trial is to determine if HSPPC-96 can be made from the tumor tissue of patients with resectable non-small cell lung cancer.
Secondary Outcomes: The secondary goals are to further characterize the safety and efficacy profile, to evaluate disease recurrence in patients, and to evaluate overall survival in patients receiving HSPPC-96.
Expected Total Enrollment:  20

Antigenics is enrolling patients in a Phase II study testing the feasibility to derive an autologous investigational vaccine (HSPPC-96) from the tumor tissue of patients with resectable non-small cell lung cancer. All patients will undergo surgery to remove the tumor and will be followed for recurrence and overall survival.

The primary goal of this trial is to determine if HSPPC-96 can be made from the tumor tissue of patients with resectable non-small cell lung cancer. The secondary goals are to further characterize the safety and efficacy profile, to evaluate disease recurrence in patients receiving, and to evaluate overall survival in patients receiving HSPPC-96.

HSPPC-96 is an investigational, immunotherapeutic agent made from an individual patient’s own tumor, which is collected at the time of surgery. A portion of the tumor tissue is sent to Antigenics’ manufacturing facility where it will undergo processing to create a vaccine. This vaccine may help the patient’s immune system attack cancerous cells while leaving healthy cells alone.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

This is a summary of criteria. Only the Principal Investigator can determine eligibility.

Inclusion Criteria:

• Suspected non-small cell lung cancer, Stage IB, Stage II, or Stage IIIA
• Tumor size > 3x3 cm or equivalent to a 9 cm² lesion
• Scheduled surgery with curative intent
• At least 18 years of age
• Must not be pregnant or breast feeding
• Agree to not receive any other investigative agent at any time while enrolled in this study

Exclusion Criteria:

• Previous treatment for non-small cell lung cancer
• Clinical signs or symptoms of brain metastases
• History of immune suppression or autoimmune disorder
• Severe active infection or other serious medical illness, that in the opinion of the Principal Investigator, would prevent study completion
• Other malignancies in the past 5 years, except adequately treated in situ cervix carcinoma or non-melanoma skin cancer

Medical Communications      1-866-805-8994    clinicalaffairs@antigenics.com

United Kingdom
      London,  United Kingdom; Recruiting

Study ID Numbers:  C-100-26
Record last reviewed:  February 2005
Last Updated:  February 3, 2005
Record first received:  December 3, 2004
ClinicalTrials.gov Identifier:  NCT00098085
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08