Enrolling by invitationNot applicableNCT07221773
Pilot Study to Evaluate the Efficacy and Safety of Xvie Delivered Into the Scalp by Microneedling in Women With Self-perceived Thinning Hair
Studying Alopecia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Restore Biologics Holdings, Inc. dba Xtressé
- Principal Investigator
- Melissa Y Rayner, MS, M.DRestore Biologics Holding, Inc dba Xtressé
- Intervention
- XVIE(other)
- Enrollment
- 15 target
- Eligibility
- 28-65 years · FEMALE
- Timeline
- 2025 – 2026
Study locations (2)
- Advanced Dermatology & Cosmetic Surgery, Maitland, Florida, United States
- Kindred Hair & Skin Center, Marriottsville, Maryland, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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