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Durvalumab for Non-Small Cell Lung Cancer
Phase 2
Waitlist Available
Led By Catherine Shu, MD
Research Sponsored by Catherine Shu
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 36 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests if it is safe and possible to use two immunotherapy drugs, durvalumab and tremelimumab, for lung cancer patients who have finished standard treatment but still have cancer DNA in their blood. The goal is to see if these drugs can help the immune system fight any remaining cancer cells. Durvalumab and tremelimumab are immune checkpoint inhibitors that have been considered for the treatment of different types of cancers, including lung cancer.
Eligible Conditions
- Non-Small Cell Lung Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 36 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~36 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Number of evaluable patients enrolled
Secondary study objectives
Adverse events rate
Disease free survival
Overall survival
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: durvalumab+ tremelimumabExperimental Treatment2 Interventions
durvalumab will be administered Q4weeks and tremelimumab will be administered Q8 weeks
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Durvalumab
2017
Completed Phase 2
~3750
Tremelimumab
2017
Completed Phase 2
~3070
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Who is running the clinical trial?
Catherine ShuLead Sponsor
1 Previous Clinical Trials
2 Total Patients Enrolled
Catherine Shu, MDPrincipal InvestigatorColumbia University
2 Previous Clinical Trials
41 Total Patients Enrolled
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