Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Revance Therapeutics, Inc.
Approximately 150 subjects, recruited from approximately 20 study centers in the United States (US) will be randomized to DAXI (HIGH-dose; LOW-dose) or placebo group, respectively.
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Written informed consent, including authorization to release health information.
Male or female subjects 18 to 65 years of age with diagnosis of unilateral plantar fasciitis.
Persistent heel pain.
Women of child bearing potential must have a negative pregnancy test at Screening and Injection Visits and must use an effective method of contraception during the course of the study.
You may not be if
Previous injection of botulinum toxin in the lower extremities or feet.
Previously suffered a partial or full thickness tear or surgery of the plantar fascia within the 5 years preceding participation in the investigation.
Pregnant, nursing, or planning a pregnancy during the study.
Current enrollment in an investigational drug or device study or participation in such a study within the last 30 days prior to first visit.
Any condition or situation which, in the Investigator's opinion, puts the subject at significant risk, could confound the trial results, or may interfere significantly with the subject's participation in the trial.
Clareo Health | DaxibotulinumtoxinA for Injection for the Treatment of Plantar Fasciitis
