RegrowProtocol

Trial pipeline · NCT06602232

A Study of DR-01 in Subjects With Alopecia Areata and Vitiligo

Phase 1 Active, not recruiting status last verified 2026-07

A registered clinical trial, reproduced from its ClinicalTrials.gov record. Every value on this page is a field on that record. Nothing on this page is a finding, an assessment or a recommendation.

The registered record

Accession number
NCT06602232
Lead sponsor
Dren Bio (industry)
Registered condition naming hair loss
Alopecia Areata
Also registered on this record
Vitiligo
Official title
A Pilot, Safety and Clinical Activity, Phase 1b Study of DR-01 in Adults With Alopecia Areata or Vitiligo

The first row holds the registered condition that placed this trial on the pipeline; the second holds everything else the sponsor registered on the same record. Both are shown, and shown apart rather than shaded differently, because leaving the second out would make this trial look more like a hair-loss study than its registration says it is — and because a distinction carried only by colour is not a distinction for every reader.

Interventions

  • DrugDR-01

Names and types as registered. The sponsors' free-text descriptions of these interventions are not reproduced: they are written by the party with an interest in the result, and reprinting them inside this site's layout would lend them this site's voice.

Design

Study type
interventional
Phase
Phase 1
Allocation
randomized
Masking
none
Primary purpose
treatment
Enrolment
81 participants (actual)
Sites
20 locations in Australia, New Zealand, United States

What it measures

  1. Incidence and severity of adverse events as assessed by CTCAE v5.0.(Safety and Tolerability)

    Time frame: Up to 12 months

  2. Mean change from baseline in SALT score

    Time frame: At week 24

  3. Mean change from baseline in VASI measures

    Time frame: At week 24

Primary outcome measures only, as registered. What a trial chose to measure, and when, is the most informative thing about it that is knowable before it reports — a hair-count endpoint at 24 weeks and a patient-satisfaction endpoint at 12 weeks are not the same study.

Who can take part

Sex
all
Age
18 Years
Healthy volunteers
not accepted

A summary of three registered fields, not the eligibility criteria. The full inclusion and exclusion criteria, the recruiting sites and the study contacts are on the registry record, which is the only place they are maintained. This site has no relationship with this trial and cannot refer anyone to it.

Registered dates

Study start
30 October 2024 (actual)
Primary completion
May 2027 (estimated)
Study completion
May 2027 (estimated)
First posted
19 September 2024 (actual)
Last update posted
8 July 2026 (actual)

"Estimated" and "actual" are the registry's own labels: an estimated date is a plan, and plans move. A date is printed at the precision it was registered at: a primary completion registered as 2027-05 is a month, and rendering it as 1 May 2027 would invent a day the sponsor did not register.

Results

This trial has not reported results. ClinicalTrials.gov holds no results record for it. That is the ordinary state of a trial that is running or about to run, and it means there is nothing here to tell you about whether the intervention works — including nothing negative. If this page implied otherwise it would be wrong.

On this site

Guides covering the condition this trial is registered for. They are about published evidence; this page is about a registration, and the two do not overlap.

Where this came from

Read from the ClinicalTrials.gov API on 6 September 2026 and rebuilt into this page without alteration. ClinicalTrials.gov is a service of the U.S. National Library of Medicine and is the authority on this record; where this page and the registry disagree, the registry is right. This page is not affiliated with or endorsed by NLM or NIH, or with the sponsor of this trial.

Open NCT06602232 on ClinicalTrials.gov · All 157 trials in the pipeline