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Completed Phase 3 Interventional Results available

Efficacy and Safety of Depemokimab (GSK3511294) in Participants With Chronic Rhinosinusitis With Nasal Polyps

ClinicalTrials.gov ID: NCT05274750

Public ClinicalTrials.gov record NCT05274750. 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 Jul 22, 2026, 11:34 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 Randomised, Double-blind, Parallel Group Phase III Study to Assess the Efficacy and Safety of 100 mg SC Depemokimab in Patients With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP) - ANCHOR-1 (depemokimAb iN CHrOnic Rhinosinusitis)

Study identification

NCT ID
NCT05274750
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
276 participants

Conditions and interventions

Conditions

Interventions

  • Depemokimab (GSK3511294) Biological
  • Placebo Drug

Biological · Drug

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
Apr 21, 2022
Primary completion
Jul 29, 2024
Completion
Aug 26, 2024
Last update posted
Dec 2, 2025

2022 – 2024

United States locations

U.S. sites
26
U.S. states
17
U.S. cities
25
Facility City State ZIP Site status
GSK Investigational Site Tucson Arizona 85704
GSK Investigational Site Buena Park California 90621
GSK Investigational Site Los Angeles California 90006
GSK Investigational Site San Diego California 91942
GSK Investigational Site Stanford California 94304
GSK Investigational Site Temecula California 92592
GSK Investigational Site Aurora Colorado 80045
GSK Investigational Site Gainesville Florida 32605
GSK Investigational Site Tamarac Florida 33321
GSK Investigational Site Tampa Florida 33613
GSK Investigational Site Meridian Idaho 83642
GSK Investigational Site Meridian Idaho 83706
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site Lexington Kentucky 40509
GSK Investigational Site Louisville Kentucky 40205
GSK Investigational Site Boston Massachusetts 02135
GSK Investigational Site New Brunswick New Jersey 08901
GSK Investigational Site Great Neck New York 11021
GSK Investigational Site Rochester New York 14642
GSK Investigational Site Chapel Hill North Carolina 27599
GSK Investigational Site Cincinnati Ohio 45267
GSK Investigational Site Tulsa Oklahoma 74137
GSK Investigational Site Bethlehem Pennsylvania 18017
GSK Investigational Site Providence Rhode Island 02914
GSK Investigational Site Dallas Texas 75390-9035
GSK Investigational Site Richmond Virginia 23235

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 79 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05274750, 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 Dec 2, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05274750 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →