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| Sponsors and Collaborators: |
ImClone Systems Merck KGaA European Organization for Research and Treatment of Cancer |
| Information provided by: | ImClone Systems |
| ClinicalTrials.gov Identifier: | NCT00037713 |
Purpose
This trial is designed to test the impact of adjuvant BEC2 (2.5 mg)/BCG vaccination on survival in patients with LD Small Cell Lung Cancer (SCLC). Patients will be stratified by institution, KPS (60 - 70% vs 80 - 100%), and response to first line combined modality therapy (CR vs PR) that consisted of at least a 2 drug regimen (4 - 6 cycles) and a chest radiotherapy regimen. Patients will be randomized to one of two treatment arms: standard arm (Observational cohort) or best supportive care, or the treatment arm (5 intradermal vaccinations of BEC2 (2.5 mg) + BCG given on day 1 of weeks 0, 2, 4, 6, and 10.
| Condition | Intervention | Phase |
|
Carcinoma, Small Cell Lung |
Biological: BEC2 Vaccine |
Phase III |
| MedlinePlus related topics: | Cancer Lung Cancer |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Open Label, Placebo Control, Safety/Efficacy Study |
| Official Title: | The SILVA Study: Survival in an International Phase III Prospective Randomized LD Small Cell Lung Cancer Vaccination Study With Adjuvant BEC2 and BCG |
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | SILVA EORTC 08971 |
| First Received: | May 20, 2002 |
| Last Updated: | September 5, 2007 |
| ClinicalTrials.gov Identifier: | NCT00037713 |
| Health Authority: | United States: Food and Drug Administration |
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