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Active, not recruiting Phase 2 Interventional

A Study to Assess the Efficacy and Safety of Efgartigimod PH20 SC in Adults With Systemic Sclerosis

ClinicalTrials.gov ID: NCT06655155

Public ClinicalTrials.gov record NCT06655155. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 4:27 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blinded, Placebo-Controlled, Phase 2, Parallel-Group Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacodynamics, Pharmacokinetics, and Immunogenicity of Efgartigimod PH20 SC in Adult Participants With Systemic Sclerosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main purpose of this study is to evaluate the effect and safety of efgartigimod PH20 SC compared to placebo in adults with systemic sclerosis. The study consists of a screening period, a treatment period of up to 48 weeks and a safety follow-up period. After the screening period, eligible participants will be randomized in a 2:1 ratio to receive either efgartigimod PH20 SC or placebo. The total study duration can be up to approximately 15 months. More information can be found on: https://clinicaltrials.argenx.com/esscape

Study identification

NCT ID
NCT06655155
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
argenx
Industry
Enrollment
87 participants

Conditions and interventions

Interventions

Combination Product · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 11, 2024 (Actual)
Primary completion
Mar 2027 (Estimated)
Completion
Oct 2027 (Estimated)
Last update posted
Oct 16, 2026

2024 – 2027

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Arizona Arthritis and Rheumatology Associates Phoenix Arizona 85032-9306 —
UCLA Ronald Reagan University of California Los Angeles Medical Center Los Angeles California 90095 —
IRIS Research and Development LLC Plantation Florida 33324 —
University of Illinois Health Outpatient Care Center Chicago Illinois 60612 —
DelRicht Research, LLC New Orleans Louisiana 70112 —
Johns Hopkins Asthma and Allergy Center Baltimore Maryland 21224 —
Thomas Jefferson University Columbia Maryland 21044 —
University of Michigan Hospital Ann Arbor Michigan 48109 —
Perelman Center for Advanced Medicine Philadelphia Pennsylvania 19104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 70 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06655155, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 16, 2026 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06655155 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →