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Exemestane for Non-Small Cell Lung Cancer

Phase 2
Waitlist Available
Led By Manish Patel, DO
Research Sponsored by Masonic Cancer Center, University of Minnesota
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year after enrollment
Awards & highlights

Summary

This trial is testing a therapy called exemestane in post-menopausal women with advanced lung cancer who have not responded to other treatments. Exemestane works by lowering estrogen levels, which can help slow down the growth of cancer cells.

Eligible Conditions
  • Non-Small Cell Lung Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year after enrollment
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year after enrollment for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Disease Response (RECIST)
Secondary outcome measures
Progression-free Survival
Quality of Life Assessment
Toxicity Assessment

Side effects data

From 2013 Phase 3 trial • 4740 Patients • NCT00038467
22%
Hot flushes NOS
18%
Arthralgia
16%
Fatigue
14%
Headache
13%
Insomnia
12%
Sweating increased
10%
Dizziness
10%
Hypertension NOS
9%
Back pain
9%
Nausea
6%
Osteoarthritis NOS
6%
Pain in limb
6%
Depression
6%
Weight increased
5%
Osteoporosis NOS
4%
Vaginal haemorrhage
1%
Abdominal pain
1%
Condition aggravated
100%
80%
60%
40%
20%
0%
Study treatment Arm
Exemestane
Tamoxifen

Trial Design

1Treatment groups
Experimental Treatment
Group I: Exemestane TherapyExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Exemestane
2003
Completed Phase 4
~7630

Find a Location

Who is running the clinical trial?

Masonic Cancer Center, University of MinnesotaLead Sponsor
276 Previous Clinical Trials
14,857 Total Patients Enrolled
Manish Patel, DOPrincipal InvestigatorUniversity of Minnesota Masonic Cancer Center
~1 spots leftby Sep 2025