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Completed Phase 3 Interventional Results available

Efficacy and Safety of Depemokimab (GSK3511294) in Participants With Chronic Rhinosinusitis With Nasal Polyps (ANCHOR-2)

ClinicalTrials.gov ID: NCT05281523

Public ClinicalTrials.gov record NCT05281523. 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 19, 2026, 8:13 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-2 (depemokimAb iN CHrOnic Rhinosinusitis)

Brief summary

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

This study will evaluate the efficacy and safety of depemokimab (GSK3511294) in participants with Chronic rhinosinusitis with nasal polyps (CRSwNP).

Study identification

NCT ID
NCT05281523
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
264 participants

Conditions and interventions

Conditions

Interventions

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 18, 2022 (Actual)
Primary completion
Jul 12, 2024 (Actual)
Completion
Aug 6, 2024 (Actual)
Last update posted
Sep 9, 2025

2022 – 2024

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
GSK Investigational Site Tucson Arizona 85724 —
GSK Investigational Site Roseville California 95661 —
GSK Investigational Site New Haven Connecticut 06520 —
GSK Investigational Site Hialeah Florida 33012 —
GSK Investigational Site Baltimore Maryland 21287 —
GSK Investigational Site Grand Rapids Michigan 55446 —
GSK Investigational Site Columbia Missouri 65212 —
GSK Investigational Site Oklahoma City Oklahoma 73120 —
GSK Investigational Site Fort Worth Texas 76109 —
GSK Investigational Site McAllen Texas 78503 —
GSK Investigational Site McKinney Texas 75070 —
GSK Investigational Site San Antonio Texas 78258 —
GSK Investigational Site Norfolk Virginia 23507 —
GSK Investigational Site Morgantown West Virginia 26506-9200 —

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 NCT05281523, 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 Sep 9, 2025 · Synced Oct 19, 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 public registry record, listed eligibility criteria, and available contact information for NCT05281523 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →