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HMG-CoA Reductase Inhibitor

Atorvastatin for Melanoma

Phase 2
Recruiting
Led By Wesley Yu, M.D.
Research Sponsored by OHSU Knight Cancer Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
DecisionDx Melanoma test result completed and resulted as class 2B
Participant must have no evidence of metastatic disease on imaging as determined by investigator assessment. All suspicious lesions amenable to biopsy should be confirmed negative for malignancy
Must not have
Participants who are currently taking a statin or have taken a statin in the year before enrollment
Participant who has a history of severe hypersensitivity (>= grade 3) attributed to compounds of similar chemical or biologic composition to atorvastatin or other agents used in the study
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from randomization to death due to any cause, assessed up to 5 years

Summary

This trial tests if atorvastatin can prevent metastasis of high-risk stage IIA melanoma, which can spread & reduce survival time. Statins may block a critical step towards melanoma metastasis & improve outcomes.

Who is the study for?
This trial is for adults over 18 with a specific type of skin cancer called high-risk stage IIA cutaneous melanoma that's been surgically removed. They must not have had other melanoma treatments or certain medications, and should be generally healthy with no evidence of cancer spread. Women who can get pregnant must agree to use birth control.
What is being tested?
The study tests if atorvastatin, commonly used for cholesterol, can prevent the spread (metastasis) of resected high-risk melanoma by affecting tumor cell behavior and immune response. Participants will either receive atorvastatin or a placebo while being monitored through scans and health records.
What are the potential side effects?
Atorvastatin may cause muscle pain, liver changes, digestive issues, and in rare cases severe allergic reactions. It might also affect pregnancy; hence women capable of childbearing need to use contraception during the trial.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My melanoma test result is class 2B.
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My scans show no signs of cancer spread, and any suspicious areas have been tested and are not cancerous.
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I can take care of myself but might not be able to do heavy physical work.
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My liver tests, specifically ALT, are within normal limits.
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I have only had surgery for my melanoma, with no prior radiation therapy.
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My skin cancer was confirmed and fully removed; it was stage IIA.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I am currently on a statin or was on one in the past year.
Select...
I have had a severe allergic reaction to atorvastatin or similar medications.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from randomization to death due to any cause, assessed up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and from randomization to death due to any cause, assessed up to 5 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Recurrence-free survival (RFS)
Secondary study objectives
Distant metastasis-free survival (DMFS)
Overall survival (OS)

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Arm II (Atorvastatin)Experimental Treatment4 Interventions
Patients receive atorvastatin PO once per day in the absence of disease progression or unacceptable toxicity for up to 5 years and undergo CT and/or MRI throughout the study.
Group II: Arm I (Placebo)Placebo Group4 Interventions
Patients receive placebo PO once per day in the absence of disease progression or unacceptable toxicity for up to 5 years and undergo CT and/or MRI throughout the study.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Atorvastatin
1998
Completed Phase 4
~10900
Computed Tomography
2017
Completed Phase 2
~2740
Magnetic Resonance Imaging
2017
Completed Phase 3
~1160

Find a Location

Who is running the clinical trial?

OHSU Knight Cancer InstituteLead Sponsor
236 Previous Clinical Trials
2,089,430 Total Patients Enrolled
2 Trials studying Cutaneous Melanoma
117 Patients Enrolled for Cutaneous Melanoma
Oregon Health and Science UniversityOTHER
1,006 Previous Clinical Trials
7,413,822 Total Patients Enrolled
2 Trials studying Cutaneous Melanoma
117 Patients Enrolled for Cutaneous Melanoma
Kuni FoundationUNKNOWN
2 Previous Clinical Trials
122 Total Patients Enrolled
~100 spots leftby Mar 2028