CPG 7909 Injection in Non-Small Cell Lung Cancer

Completed · Phase 2

Conditions studied: Carcinoma, Non-Small Cell Lung

In brief

Eligible patients will be randomized in a ratio of 2:1 to receive either chemotherapy (a taxane and a platinum compound) plus CPG 7909 Injection or chemotherapy alone. Protocol therapy will be administered until disease progression or intolerable toxicity. CpG 7909 Injection will be administered subcutaneously, on Weeks 2 and 3 of each three-week cycle (days 8 and 15) and chemotherapy will be administered on Week 1 (Day 1). Patients will undergo complete disease evaluation at the end of every other treatment cycle until disease progression.

Key facts

Study ID
NCT00070629
Run by
Pfizer
People needed
116
Starts
2003-05-01
Expected to finish
2007-07-01
Last updated by the study team
2009-02-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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