Skip to content
Bored Studies
RecruitingAccepts healthy volunteersPhase 1

First-in-Human Trial to Assess REGN20423 in Healthy Adult Participants and Adult Participants With Atopic Dermatitis

Regeneron Pharmaceuticals · NCT07527923

View Study & Apply (opens in a new tab)

Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–65 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Phase 1
Target enrollment
144
US sites recruiting
6
Study start
May 22, 2026
Record last updated
October 7, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This study will test a study medicine called REGN20423 to see how effective it is in healthy participants (in Part A) and participants with atopic dermatitis (eczema) (in Part B). REGN20423 is a study medicine that is only used in clinical studies. REGN20423 has not previously been studied in humans.

The study is looking at

  • What side effects REGN20423 might cause
  • How much REGN20423 is in the blood at different times
  • How well REGN20423 works in adults with atopic dermatitis
  • Whether the body makes antibodies against REGN20423
  • How the body changes after having REGN20423, which can help researchers understand why REGN20423 works better in some people than others
  • What the best dose of REGN20423 is

Being studied: REGN20423; Placebo

Conditions: Healthy Volunteer; Atopic Dermatitis

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Part A: Enrolls healthy participants Part B: Enrolls participants with atopic dermatitis

Key Inclusion Criteria

Part A

  • Is judged by the investigator to be in good health based on medical history, physical examination, vital signs, Electrocardiograms (ECGs), and laboratory safety testing at screening and prior to initial dose of study intervention
  • Has a BMI within 18 to 31 kg/m² (inclusive) at the screening visit

Part B

  • Has a history of AD for at least 6 months at screening
  • Has EASI score ≥5 at both the screening and baseline visits
  • Has IGA score ≥2 at both the screening and baseline visits

Key Exclusion Criteria

Part A

  • Hospitalized (>24 hours) for any reason within 30 days prior to the screening visit
  • Hypersensitivity to the study treatment or any of its excipients
  • History of clinical parasite infection, except treated trichomoniasis
  • Received a live attenuated vaccine within 1 month prior to the first screening visit or anticipates need for a live attenuated vaccine during the study
  • History of alcohol or drug abuse as determined by the investigator

Part B

  • Known or suspected history of immunosuppression
  • Presence of skin comorbidities at screening that may interfere with study assessments
  • Inability to discontinue medications and treatments prior to baseline and during the study per the Excluded Medications and Treatments list
  • Uncontrolled chronic disease that might require bursts of oral corticosteroids during the study

Note: Other protocol defined Inclusion/ Exclusion criteria apply

Recruiting US locations

Study contacts (from the official record)

  • Clinical Trials Administrator · 844-734-6643 · clinicaltrials@regeneron.com
All dermatology studies in Alabama →