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Completed Phase 2 Interventional Results available

Study Testing Response Effect of KY1005 Against Moderate-to-Severe Atopic Dermatitis, The STREAM-AD Study

ClinicalTrials.gov ID: NCT05131477

Public ClinicalTrials.gov record NCT05131477. 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 May 8, 2026, 5:02 AM 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 Phase IIb, Randomized, Double-blind, Placebo-controlled, Parallel Group, Multicenter Dose Ranging Study of a Subcutaneous Anti-OX40L Monoclonal Antibody (KY1005) in Moderate-to-Severe Atopic Dermatitis

Study identification

NCT ID
NCT05131477
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kymab Limited
Industry
Enrollment
390 participants

Conditions and interventions

Interventions

  • Amlitelimab Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Dec 12, 2021
Primary completion
Apr 25, 2023
Completion
Feb 20, 2024
Last update posted
Jul 2, 2025

2021 – 2024

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Investigative Site Number: 1018 Fremont California 94538-1601
Investigative site #1022 Sacramento California 95816-3370
Investigative Site Number: 1006 Boca Raton Florida 33428
Investigative Site Number: 1001 Clearwater Florida 33756-3424
Investigative Site Number: 1019 Coral Gables Florida 33134-2950
Investigative Site Number: 1007 Miami Florida 33176-2264
Investigative Site Number: 1013 Tampa Florida 33615-3816
Investigative Site Number: 1004 Savannah Georgia 31406-2668
Investigative Site Number: 1010 Clarksville Indiana 47129-2201
Investigative Site Number: 1015 Indianapolis Indiana 46250-2041
Investigative Site Number: 1021 Louisville Kentucky 40241
Investigative Site Number: 1011 Towson Maryland 21204-7448
Investigative Site Number: 1014 Beverly Massachusetts 01915-1666
Investigative Site Number: 1012 Troy Michigan 48084-3536
Investigative Site Number: 1005 Tulsa Oklahoma 74136-7049
Investigative Site Number: 1017 Portland Oregon 97223-6683
Investigative Site Number: 1009 Portland Oregon 97239
Investigative Site Number: 1003 Anderson South Carolina 29621-2062
Investigative Site Number: 1008 Murfreesboro Tennessee 37130-2450
Investigative site #1023 Mansfield Texas 76063

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 83 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05131477, 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 Jul 2, 2025 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05131477 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →