MRG-110 is intended to promote the growth of new blood vessels by inhibiting a molecule called miR-92a. MRG-110 is being studied to determine if it can accelerate healing of wounds by improving blood flow into the wound area. The primary objective of this study is to investigate the safety and tolerability of MRG-110 when injected into the skin at the site of a small skin wound in normal healthy volunteers. Another objective is to study the pharmacokinetics of MRG-110 (the movement of a drug into, through and out of the body). Participants in the clinical trial will receive either a single dose or multiple doses of MRG-110 and/or placebo. Blood samples, urine samples and skin biopsies will be collected to measure how MRG-110 is processed by the body, and how the body responds when exposed to MRG-110.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
42
Single ascending doses of MRG-110
Single doses of placebo
Multiple ascending doses of MRG-110
Multiple doses of Placebo
Celerion, Inc.
Lincoln, Nebraska, United States
Number of participants with treatment-related adverse events as assessed by CTCAE v4.03.
Time frame: Up to Day 55
Area under the plasma concentration vs. time curve (AUC) of MRG-110 following single and repeat doses.
Time frame: Up to Day 45
Peak plasma concentration (Cmax) of MRG-110 following single and repeat doses
Time frame: Up to Day 45
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