Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-dose Study to Evaluate the Efficacy and Safety of VDPHL01 in Male Subjects With Androgenetic Alopecia

Next Previous
Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-dose Study to Evaluate the Efficacy and Safety of VDPHL01 in Male Subjects With Androgenetic Alopecia

Status: Active, no longer recruiting
Phase of Trial: Phase II/III

Latest Information Update: 30 Apr 2026

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs VDPHL (Primary)
  • Indications Male pattern baldness
  • Focus Registrational; Therapeutic Use
  • Sponsors Veradermics

Most Recent Events

  • 26 Apr 2026 According to Veradermics media release, topline data from the trial will be presented via company webcast.
  • 09 Feb 2026 According to Veradermics media release, topline data from this study is anticipated in 1H 2026.
  • 09 Feb 2026 According to Veradermics media release, the company is advancing towards the NDA filing for the oral treatment (VDPHL) for pattern hair loss.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top