Een studie ter evaluatie van de werkzaamheid en veiligheid van SM04554-topische oplossing bij mannelijke proefpersonen met androgenetische alopecia
Multicenter, gerandomiseerde, dubbelblinde, placebogecontroleerde studie van de werkzaamheid en veiligheid van 0,15% en 0,25% concentraties van actuele SM04554-oplossing bij mannelijke proefpersonen met androgenetische alopecia
This multi-center, randomized, double-blind, placebo-controlled study, conducted in Turkey, will assess the efficacy and safety of topical SM04554 solution (0.15% and 0.25%) applied daily to the scalp of male androgenetic alopecia (AGA) subjects.
Studie Overzicht
Toestand
Conditie
Gedetailleerde beschrijving
This study was a multicenter, randomized, double-blind, placebo-controlled, parallel-group study conducted in Turkey of 2 different strengths of topical SM04554 solution applied QD to the scalp of male androgenetic alopecia (AGA) subjects - otherwise known as male pattern baldness.
Following a screening period of up to 2 weeks, subjects participated in the study for 54 weeks (48 weeks of treatment and 6 weeks of follow-up). Subjects were randomized into 1 of 3 groups in a 2:2:1 randomization scheme: SM04554 0.15% solution, SM04554 0.25% solution, and vehicle placebo.
Primary outcome of this study was change in absolute hair count as assessed by phototrichogram, a non-invasive and reproducible method to measure changes in hair.
Studietype
Inschrijving (Werkelijk)
Fase
- Fase 2
- Fase 3
Contacten en locaties
Studie Locaties
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Ankara, Turkije (Türkiye), 06100
- Research Site
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Ankara, Turkije (Türkiye), 06110
- Research Site
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Ankara, Turkije (Türkiye), 06680
- Research Site
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Bursa, Turkije (Türkiye), 16059
- Research Site
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Denizli, Turkije (Türkiye), 20070
- Research Site
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Istanbul, Turkije (Türkiye), 34098
- Research Site
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Istanbul, Turkije (Türkiye), 34668
- Research Site
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Izmir, Turkije (Türkiye), 35180
- Research Site
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Kayseri, Turkije (Türkiye), 38039
- Research Site
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Kocaeli, Turkije (Türkiye), 41380
- Research Site
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Mersin, Turkije (Türkiye), 33343
- Research Site
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Samsun, Turkije (Türkiye), 55139
- Research Site
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Trabzon, Turkije (Türkiye), 61080
- Research Site 1
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Trabzon, Turkije (Türkiye), 61080
- Research Site 2
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Being a Turkish citizen
- Clinical diagnosis of AGA with Norwood-Hamilton Classification score of 3V or 4
- Willing to inform females, with whom they may interact, that they are using a topical investigational product and direct contact should be avoided as potential harm to a fetus is unknown
- Willing and able to attend all study visits
- Willing to maintain the same hair style and length as at the study start for the duration of the study
- Willing to not use semi-permanent hair products (e.g., color, texturizers, relaxers) for the duration of the study; daily styling products (e.g., hair gel, mousse, styling spray) will be allowed on non-study visit days
- Willing to use mild non-medicated shampoo and conditioner for the duration of the study
- Able to read and understand Turkish
- Ability to comprehend and willing to sign an informed consent form
Exclusion Criteria:
- Males who are sexually active, and have a partner who is capable of becoming pregnant, if neither has had surgery to become sterilized, and/or who are not willing to use condom or whose partner is not using a highly effective method of birth control that includes double barrier, intrauterine device, or hormonal contraceptive combined with single barrier, or abstinence during the study treatment period until 90 days post last dose of study medication
- Clinical diagnosis of alopecia areata or other non-AGA forms of alopecia
- Scalp hair loss on the treatment area, due to disease, injury, or medical therapy
- History of surgical correction (e.g., hair transplantation, scalp reduction) of hair loss on the scalp
- Previous exposure to SM04554
- Use of any products (e.g., finasteride, minoxidil, platelet rich plasma, biotin) or devices (e.g., laser light therapy) purported to promote scalp hair growth within 24 weeks prior to the start of the study
- Use of anti-androgenic therapies (e.g., spironolactone, flutamide, cyproterone acetate, cimetidine) within 12 weeks prior to the start of the study
- Use of medications that potentially cause drug-induced hair loss (e.g., depotestosterone, haloperidol, methotrexate, methylprednisolone, prednisone, testosterone, divalproex sodium) within 12 weeks prior to the start of the study
- Current use of an occlusive wig, hair extensions, or hair weaves
- History of hypersensitivity or allergies to any ingredient of the study medication
- Participation in any other investigational drug or medical device trial, which includes or included administration of an investigational study medication or medical device, within 30 days or 5 half-lives of the investigational agent, whichever is longer, prior to the start of the study
- Use of semi-permanent hair products (e.g., color, texturizers, relaxers) within 30 days prior to the start of the study
- Use of medicated shampoo or conditioner (medicated shampoo and conditioner refers to any prescription shampoo or conditioner as well as any over-the-counter medicated shampoo or conditioner, such as those for treatment of dandruff or promoting hair growth) within 30 days prior to the start of the study
- Subjects who are immediate family members (spouse, parent, child, or sibling; biological or legally adopted) of personnel directly affiliated with the study at the investigative site, or are directly affiliated with the study at the investigative site
- Subjects employed by Samumed, LLC or Samumed Turkey, or any of its affiliates or development partners (i.e., an employee, temporary contract worker, or designee) responsible for the conduct of the study
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verdrievoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Topical SM04554 0.15% solution
Topical SM04554 0.15% solution, once daily for up to 48 weeks |
Study medication application will be performed by the individual subject at approximately the same time each day. |
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Experimenteel: Topical SM04554 0.25% solution
Topical SM04554 0.25% solution, once daily for up to 48 weeks |
Study medication application will be performed by the individual subject at approximately the same time each day. |
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Placebo-vergelijker: Vehicle
Topical vehicle solution, once daily for up to 48 weeks |
Vehicle solution application will be performed by the individual subject at approximately the same time each day. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Absolute Non-vellus Hair Count in Target Area
Tijdsspanne: Week 48
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Non-vellus hair count was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Week 48
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Absolute Non-vellus Hair Count in Target Area
Tijdsspanne: Weeks 12, 24, and 36
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Non-vellus hair count was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Weeks 12, 24, and 36
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Absolute Vellus Hair Count in Target Area
Tijdsspanne: Weeks 12, 24, 36 and 48
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Vellus hair count was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Weeks 12, 24, 36 and 48
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Absolute Total Hair Count in Target Area
Tijdsspanne: Weeks 12, 24, 36 and 48
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Total hair count was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Weeks 12, 24, 36 and 48
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Change From Baseline in Non-vellus Hair Count in Target Area
Tijdsspanne: Baseline, and Weeks 12, 24, 36 and 48
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Change from baseline in non-vellus hair count in target area by PTG analysis. Non-vellus hair count was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Baseline, and Weeks 12, 24, 36 and 48
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Change From Baseline in Vellus Hair Count in Target Area
Tijdsspanne: Baseline, and Weeks 12, 24, 36 and 48
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Change from baseline in vellus hair count in target area by PTG analysis. Vellus hair count was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Baseline, and Weeks 12, 24, 36 and 48
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Change From Baseline in Total Hair Count in Target Area
Tijdsspanne: Baseline, and Weeks 12, 24, 36 and 48
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Change from baseline in total hair count in target area by PTG analysis. Vellus and non-vellus hair count was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Baseline, and Weeks 12, 24, 36 and 48
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Change From Baseline in Average Non-vellus Hair Shaft Thickness in Target Area
Tijdsspanne: Baseline, and Weeks 12, 24, 36 and 48
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Change from baseline in average non-vellus hair shaft thickness in target area by PTG analysis. Non-vellus hair shaft thickness was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. |
Baseline, and Weeks 12, 24, 36 and 48
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Change From Baseline in Average Non-vellus Hair Density in Target Area
Tijdsspanne: Baseline, and Weeks 12, 24, 36 and 48
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Change from baseline in average non-vellus hair density (cumulative non-vellus hair shaft thickness) in target area by PTG analysis. Non-vellus hair shaft thickness was determined by phototrichogram. Standardized phototrichogram images of the treatment area were taken on Visit Day 1 (pre-treatment), as well as at visits occuring at Weeks 12, 24, 36, and 48. A rectangular area of the subject's hair with dimensions 20 x 15 mm was clipped to between 0.6 and 0.9 mm in length prior to performing the phototrichogram. Virtual tattoo technology was used to anchor the phototrichogram. Images were uploaded from sites to the blinded vendor where assessment of the phototrichogram took place. For this outcome, the cumulative non-vellus hair shaft thickness in the measurement area was summarized. |
Baseline, and Weeks 12, 24, 36 and 48
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Improvement in Subject Assessment of Hair Growth
Tijdsspanne: Weeks 6, 12, 18, 24, 30, 36, 42 and 48
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Subjects will complete a questionnaire for hair growth while referencing the global scalp photograph taken at the visit as compared to their baseline global scalp photograph. The scale for the questionnaire ranges from -3 to +3 (-3 indicates the worst outcome and +3 indicates the best outcome). Improvement is defined as +1, +2, and +3: Much Better. |
Weeks 6, 12, 18, 24, 30, 36, 42 and 48
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Change From Baseline in Subject Assessment of Hair Satisfaction
Tijdsspanne: Baseline, and Weeks 6, 12, 18, 24, 30, 36, 42 and 48
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Subjects will complete a questionnaire for hair satisfaction while referencing the global scalp photograph taken at the visit as compared to their baseline global scalp photograph. The scale for the questionnaire ranges from -3 to +3 (-3 indicates the worst outcome and +3 indicates the best outcome). The change from baseline is the difference between the baseline and follow-up response. |
Baseline, and Weeks 6, 12, 18, 24, 30, 36, 42 and 48
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie directeur: Yusuf Yazici, M.D., Biosplice Therapeutics, Inc.
Studie record data
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Studieregistratiedata
Eerst ingediend
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Eerst geplaatst (Werkelijk)
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Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- SM04554-AGA-05
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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