Study to Evaluate Xtressé Gummy Supplement in Men With Androgenic Alopecia

In the study, participants will be asked to complete the following:

Provide basic personal information (including date of birth, gender, race and ethnicity) Provide their medical/ surgical history and perform a medical exam (including but not limited to symptom-directed physical exam, skin type, vital signs, height, weight) Follow study rules such as avoiding certain medications and treatments Provide information on any medications, treatments or reactions that started after the study began Take gummy treatment daily and complete a treatment diary Allow clinical assessments and documentation of the treatment, such as photography, hair density measurements, any reactions or side effects

To qualify for this trial, participants must:

Be a male adult between 18 to 65 years of age Have hair loss in vertex region. Give voluntary written consent Be willing to follow study instructions and complete study requirements, including maintaining current diet and hair care routine, not using non-approved lotions and creams on the treatments areas Allow photographs of the front and top area of the scalp Confirm they are not sensitive to any of the study treatment ingredients

All photographs of the treatment area collected during the study will be used as study data.

All participants have the right to refuse further participation in the study at any time.

Inclusion criteria

• Males aged 18-65
• Norwood III to IV, vertex focused
• Fitzpatrick skin type I to VI
• Ability and willingness to comply with study protocol

Exclusion criteria

• Change in other hair treatments in 3 months prior to study enrollment.
• Known uncontrolled health conditions.
• History of hair or scalp disorders that could interfere with study results.
• History of metabolic syndrome.