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Cutaneous Biopsy for microarray analysis for Melanoma (RATIO Trial)
N/A
Waitlist Available
Led By Michael Smylie, MB, FRCPC
Research Sponsored by AHS Cancer Control Alberta
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 24 months
Awards & highlights
RATIO Trial Summary
This study is evaluating whether a new diagnostic system can detect melanoma in biopsies.
Eligible Conditions
- Melanoma
RATIO Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Correlation of the MMDx from pretreatment biopsy with overall response rate (ORR).
Secondary outcome measures
Overall Survival (OS)
Progression Free Survival (PFS)
RATIO Trial Design
1Treatment groups
Experimental Treatment
Group I: Cutaneous Biopsy for microarray analysisExperimental Treatment1 Intervention
To determine whether outcomes improve as a function of anti-tumor immunity which may enable the use of this technique as a predictive biomarker of treatment response.
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Who is running the clinical trial?
Transplant Genomics, Inc.Industry Sponsor
13 Previous Clinical Trials
3,965 Total Patients Enrolled
AHS Cancer Control AlbertaLead Sponsor
182 Previous Clinical Trials
36,177 Total Patients Enrolled
1 Trials studying Melanoma
11 Patients Enrolled for Melanoma
Michael Smylie, MB, FRCPCPrincipal InvestigatorAlberta Health services
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