Open-Label Extension of Other SZ1839 (Iressa) Trials
Phase 3
Completed
- Conditions
- Cancer
- Registration Number
- NCT00635973
- Lead Sponsor
- AstraZeneca
- Brief Summary
A trial to assess patients who have been treated with Iressa in a previous clinical trial and may benefit from continued treatment with Iressa.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- Received treatment in a previous Iressa clinical trial
- Provided Informed Consent to participate in the trial
- 30 days or less since completing the previous Iressa trial.
Exclusion Criteria
- Radiotherapy completed more than 14 days before starting treatment in this trial
- Incomplete healing from prior surgery
- Withdrawal from previous Iressa trial due to unacceptable toxicity to major organs
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Adverse Events Every 28 days
- Secondary Outcome Measures
Name Time Method Progression Free Survival Every 28 days Survival Every 28 days
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms of ZD1839 (Iressa) in cancer treatment beyond EGFR inhibition?
How does ZD1839 (Iressa) compare to other tyrosine kinase inhibitors in non-small cell lung cancer management?
Which biomarkers correlate with sustained response to ZD1839 (Iressa) in metastatic cancer patients?
What are the long-term adverse event profiles of ZD1839 (Iressa) in extended monotherapy regimens?
How do ZD1839 (Iressa) combination therapies compare to monotherapy in EGFR-mutated cancer treatment outcomes?