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NCT06527365 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy of VDPHL01 in Males and Females With AGA

A Phase 2 study of Androgenetic Alopecia and AGA, sponsored by Veradermics.

Active
Registry status
Phase 2
Development phase
70
Enrollment target
4
Study locations

NCT06527365 is a Phase 2 study of Androgenetic Alopecia and AGA that is active but no longer recruiting, run by Veradermics. The registered enrollment target is 70 participants, below the 160-participant average among 16 other Androgenetic Alopecia trials with a reported enrollment target (56% lower). The trial reports 4 study locations across 4 states.

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The verdict

NCT06527365, a Phase 2 study of Androgenetic Alopecia and AGA, is active but no longer recruiting, sponsored by Veradermics.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
70 participants
Enrollment target
4
Study locations

Study Summary

This study will evaluate the safety and efficacy of VDPHL01 in male and female subjects with Androgenetic Alopecia (AGA). AGA (or pattern of hair loss) is a genetic disorder caused by an excessive (too much) hair follicle response to androgens (hormone) that causes hair loss. VDPHL01 8.5 mg Tablets for males and VDPHL01 4.5 mg Tablets for females are an investigational oral drug to treat male and female pattern baldness. This multiple center, open-label, study will last about 13 months and includes 11 study visits (screening, baseline (day 1), week 2, month 1, month 2, month 4, month 6, month 8, month 10, month 12, month 13). Male subjects that meet the study eligibility criteria will be administered VDPHL01 once daily for 12 months. Female subjects that meet the study eligibility criteria will be administered VDPHL01 either once or twice daily for 12 months.

Interventions

  • DRUG VDPHL01

Study Locations (4)

California

  • 01 - San Diego

Indiana

  • 04 - New Albany

New Jersey

  • 03 - Hackensack

Utah

  • 02 - South Jordan

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2024-07-08
Est. Completion 2026-08
Phase Phase 2

Sponsor

Veradermics

5 total trials

What the Registry Record Tells You About NCT06527365

The ClinicalTrials.gov registry entry for NCT06527365 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 160-participant average among 16 other Androgenetic Alopecia trials with a reported enrollment target (56% lower). The listed sponsor is Veradermics, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Androgenetic Alopecia appearing as the primary indexed condition, and to 1 intervention - of which VDPHL01 is the first listed.

NCT06527365 reports 4 study locations spanning 4 distinct geographic areas - top geographies include California, Indiana, New Jersey.

Frequently Asked Questions

What is clinical trial NCT06527365 about?

NCT06527365 is a clinical study titled "Safety and Efficacy of VDPHL01 in Males and Females With AGA". This study will evaluate the safety and efficacy of VDPHL01 in male and female subjects with Androgenetic Alopecia (AGA). AGA (or pattern of hair loss) is a genetic disorder caused by an excessive (too much) hair follicle response to androgens (hormone) that causes hair loss. VDPHL01 8.5 mg Tablets...

What is the current status of trial NCT06527365?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 70 participants. The study started on 2024-07-08. Estimated completion is 2026-08.

What conditions does trial NCT06527365 study?

This clinical trial studies the following conditions: Androgenetic Alopecia, AGA, Male Pattern Baldness.

What interventions are being tested in trial NCT06527365?

The interventions under investigation include: VDPHL01 (DRUG).

Who is sponsoring clinical trial NCT06527365?

This trial is sponsored by Veradermics, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06527365 being conducted?

This trial has 4 study locations across California, Indiana, New Jersey, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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