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NCT03736967 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety of REGN3500 Monotherapy and Combination of REGN3500 Plus Dupilumab in Adult Patients With Moderate-to-Severe Atopic Dermatitis

A Phase 2 study, sponsored by Regeneron Pharmaceuticals.

Terminated
Registry status
Phase 2
Development phase
206
Enrollment target

NCT03736967: Clinical Trial Phase 2 study, sponsored by Regeneron Pharmaceuticals.

NCT03736967 is a Phase 2 study that was terminated before completion, run by Regeneron Pharmaceuticals. The registered enrollment target is 206 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (55% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03736967, a Phase 2 study, was terminated before completion, sponsored by Regeneron Pharmaceuticals.

TERMINATED
Registry status
Phase 2
Development phase
206 participants
Enrollment target

Study Summary

The primary objective of the study is to evaluate the efficacy of REGN3500 monotherapy compared with placebo treatment in adult patients with moderate-to-severe Atopic dermatitis (AD). Secondary Objectives are to: * Evaluate the efficacy of REGN3500 in combination with dupilumab compared with placebo treatment in adult patients with moderate-to-severe AD * Assess the safety, tolerability, and immunogenicity of subcutaneous (SC) doses of REGN3500 monotherapy and REGN3500 in combination with dupilumab in adult patients with moderate-to-severe AD * Evaluate the Pharmacokinetic (PK) of REGN3500 monotherapy and REGN3500 in combination with dupilumab in adult patients with moderate-to-severe AD

Primary Outcome

The EASI score was used to measure the severity and extent of atopic dermatitis (AD) and measures erythema, induration, excoriation and lichenification on 4 anatomic regions of the body: head, trunk, upper and lower extremities. The total EASI score ranges from 0 (minimum) to 72 (maximum) points, with the higher scores reflecting the worse severity of AD. Percent change from baseline in EASI score at Week 16 based on observed values set to missing after rescue treatment was reported. Values afte

Interventions

  • DRUG Placebo
  • DRUG Dupilumab
  • DRUG REGN3500
  • DRUG REGN3500 + Dupilumab Combo

Trial Details

FieldValue
Enrollment Target 206 participants
Start Date 2018-11-12
Est. Completion 2020-07-28
Phase Phase 2
Regeneron Pharmaceuticals

280 total trials

Why NCT03736967 stopped before completion

NCT03736967 is an interventional study that assigns participants to a tested intervention. The registered 206 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (55% higher).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT03736967 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03736967 about?

NCT03736967 is a clinical study titled "Efficacy and Safety of REGN3500 Monotherapy and Combination of REGN3500 Plus Dupilumab in Adult Patients With Moderate-to-Severe Atopic Dermatitis". The primary objective of the study is to evaluate the efficacy of REGN3500 monotherapy compared with placebo treatment in adult patients with moderate-to-severe Atopic dermatitis (AD). Secondary Objectives are to: * Evaluate the efficacy of REGN3500 in combination with dupilumab compared with plac...

What is the current status of trial NCT03736967?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 206 participants. The study started on 2018-11-12. Estimated completion is 2020-07-28.

What interventions are being tested in trial NCT03736967?

The interventions under investigation include: Placebo (DRUG), Dupilumab (DRUG), REGN3500 (DRUG), REGN3500 + Dupilumab Combo (DRUG).

Who is sponsoring clinical trial NCT03736967?

This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03736967's enrollment target sits among peer trials

206 298th of 2000 higher than 1,703 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03736967, the US trial registry maintained by the National Library of Medicine. NCT03736967 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.