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RNAi

RXI-109 for Hypertrophic Scar

Phase 2
Waitlist Available
Research Sponsored by RXi Pharmaceuticals, Corp.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9 months
Awards & highlights

Study Summary

The purpose of this study is to determine the effectiveness of RXI-109 in reducing the recurrence of hypertrophic scar formation following elective revision of a pre-existing hypertrophic scar.

Eligible Conditions
  • Hypertrophic Scar

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 9 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Reducing the recurrence of hypertrophic scar after scar revision surgery
Secondary outcome measures
Safety evaluation of RXI-109

Trial Design

1Treatment groups
Experimental Treatment
Group I: RXI-109Experimental Treatment1 Intervention
RXI-109 dosed at the site of the revised hypertrophic scar
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
RXI-109
2012
Completed Phase 2
~80

Find a Location

Who is running the clinical trial?

RXi Pharmaceuticals, Corp.Lead Sponsor
6 Previous Clinical Trials
163 Total Patients Enrolled
Pamela Pavco, PhDStudy DirectorRXi Pharmaceuticals
3 Previous Clinical Trials
124 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Who else is applying?

What site did they apply to?
NCT02246465
What portion of applicants met pre-screening criteria?
Did not meet criteria
~4 spots leftby May 2025