CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 20 enrolled
Drug / intervention
incobotulinumtoxin Adrug
Likely dose
incobotulinumtoxin A 150 unitsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05456087
NCT05456087Phase 2Active

Use of Botulinum Toxin in the Treatment of Androgenic Alopecia

Zel Skin and Laser Specialists·interventional·Posted Jul 13, 2022·Updated Mar 27, 2024

In Brief

A Phase 2 clinical trial evaluating incobotulinumtoxin A for Androgenetic Alopecia. Active but no longer recruiting, targeting 20 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate the effect of using a purified botulinum toxin (Xeomin®, Merz, USA), the same injectable used to improve face wrinkles, to treat a specific type of hair loss seen in men and women not associated with scarring or other internal disease called 'pattern hair loss'. This type of hair loss is medically called 'androgenic or androgenetic alopecia'. In men it is typically called 'male pattern baldness' whereas in women it is called 'female pattern baldness' and in both cases is hereditary meaning there will be a history of relatives that describe having the same condition.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2ActiveOverdue
2023202420252026
First PostedJul 13, 2022
Enrollment StartAug 12, 2022
Primary CompletionDec 1, 2024
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 4.0 years ago

Interventions

incobotulinumtoxin Adrug

Up to 150 units of incobotulinumtoxin A will be injected at up to 30 injection sites within the hair loss area