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Women’s Androgenetic Alopecia Study (14 Months)

For condition: Alopecia
For condition: Androgenetic Alopecia
Enrolling:
250-13951-306

Women’s Androgenetic Alopecia Study (14 Months)

Study Summary

Who Can Participate?
Women aged 18 to 65 with mild to moderate androgenetic alopecia may participate.

Inclusion Criteria
• have a clinical diagnosis of mild to moderate AGA
• willing to maintain the same hair care regimen with the same hair care products throughout the study
• willing to maintain at least ¼ inch length hair during the study with the same hairstyle, hair length, and hair color throughout the study

Participant Information
• Participate and receive study treatment at no cost
• Regular visits with study doctors who specialise in treating androgenetic alopecia (11 visits)
• Will receive either an investigative oral treatment (study drug) or an inert tablet
• Reimbursement for study-related expenses may be provided

How Long Will The Study Last?
• 62 weeks

Note: Participants will need to stop all other treatments for androgenetic alopecia during clinical trial participation. Some over-the-counter preparations may be deemed acceptable by the doctor performing the study.

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For more information about this trial, please visit ClinicalTrials.gov

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Last Revised: July 2024

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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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