A Cancer Vaccine (CG8123) Given With and Without Cyclophosphamide for Advanced Stage Non-Small Cell Lung Cancer (NSCLC)

C

Cell Genesys

Status and phase

Completed
Phase 2

Conditions

Carcinoma, Non-Small-Cell Lung
Lung Cancer

Treatments

Drug: Cyclophosphamide
Biological: CG8123

Study type

Interventional

Funder types

Industry

Identifiers

NCT00089726
D-0031

Details and patient eligibility

About

The main purpose of this research study is to determine if a vaccine made from a patient's lung cancer tumor cells will be effective in making the cancer shrink or disappear. The vaccine will be given by itself to some patients, while other patients will get the vaccine with cyclophosphamide (a type of chemotherapy). Studies in animals and other cancer vaccine trials suggest that cyclophosphamide may make tumor vaccines more potent. This study will try to determine if vaccine given with or without this chemotherapy is effective in destroying lung cancer cells. Additionally, the study will collect information on vaccine safety, both with and without chemotherapy, and whether the vaccine improves lung cancer-related symptoms (e.g., shortness of breath). Tumors from surgical resection will be processed and made into a vaccine. Prior to treatment, patients will be randomized equally to one of two treatment groups, Cohort A and Cohort B. Patients in Cohort A will be treated with CG8123 vaccine only and patients in Cohort B will be treated with CG8123 vaccine plus a single dose of cyclophosphamide administered one day prior to the first, third, and fifth vaccine treatments. Patients will receive intradermal (beneath the skin) vaccine injections every two weeks for up to eight weeks, for a total of up to five vaccine treatments. The duration of this study, including active follow up, is approximately two years. After this, patients will be followed-up yearly for a total of 15 years.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years or older
  • Suspicious diagnosis of or histologically- confirmed stage IIIB or IV non small-cell lung cancer
  • Accessible and adequate tumor source for vaccine production.
  • Tumor source for vaccine production must be accessible by a minor surgical procedure performed under local or regional anesthesia (e.g. lymph node or soft tissue mass or malignant pleural effusion)
  • Measurable disease to evaluate following tumor procurement
  • Limited metastatic tumor burden
  • Life expectancy at least 4 months
  • ECOG Performance Status 0 - 1

Exclusion criteria

  • Active and/or untreated brain metastases
  • Active or impending spinal cord compression
  • Active auto-immune disease or treatment with immunosuppressants
  • Decompensated congestive heart failure or recent significant cardiac event
  • Coexisting malignancies
  • Significant or uncontrolled medical problems or laboratory abnormalities that might increase the risk of surgical complications or vaccine treatment
  • Previous treatment with gene therapy (including any adenoviral-based therapy)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location

Resources

© Copyright 2024 Veeva Systems