Chronic Rhinosinusitis with Nasal Polyps (CRSwNP) Clinical Trials

Find Chronic Rhinosinusitis with Nasal Polyps (CRSwNP) Clinical Trials Near You

A Phase IV, Single-arm, Open-label Study to Evaluate the Efficacy and Safety of 100 mg SC Depemokimab Monotherapy Without Concomitant Use of Intranasal Corticosteroids (INCS) in Japanese Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP) Who Are Inadequately Controlled With Standard Treatment

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This study will evaluate the efficacy and safety of depemokimab (GSK3511294) without concomitant use of Intranasal corticosteroids (INCS) in participants with Chronic rhinosinusitis with nasal polyps (CRSwNP).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 18 years of age and older inclusive, at the time of signing the informed consent

• Endoscopic bilateral NP score of at least 5 out of a maximum score of 8 (with a minimum score of 2 in each nasal cavity) assessed by the investigator

• Participants who have had previous nasal surgery for the removal of nasal polyps, have used at least three consecutive days of systemic corticosteroids in the previous 2 years for the treatment of nasal polyps, or are medically unsuitable or intolerant to systemic corticosteroid

• Participants presenting with severe nasal polyp symptoms defined as symptoms of nasal congestion/blockade/obstruction with moderate or severe severity and loss of smell or rhinorrhoea (runny nose) based on clinical assessment by the investigator

• Presence of symptoms of chronic rhinosinusitis as described by at least 2 different symptoms for at least 12 weeks prior to Visit 1, one of which should be either nasal blockage/obstruction/congestion or nasal discharge (anterior/posterior nasal drip), or facial pain/pressure and/or reduction or loss of smell

• Male or eligible female participants

Locations
Other Locations
Japan
GSK Investigational Site
RECRUITING
Ehime
GSK Investigational Site
RECRUITING
Ehime
GSK Investigational Site
RECRUITING
Fukui
GSK Investigational Site
RECRUITING
Fukuoka
GSK Investigational Site
RECRUITING
Gunma
GSK Investigational Site
RECRUITING
Nagano
GSK Investigational Site
RECRUITING
Osaka
GSK Investigational Site
RECRUITING
Saitama
GSK Investigational Site
RECRUITING
Shiga
GSK Investigational Site
RECRUITING
Shizuoka
Contact Information
Primary
US GSK Clinical Trials Call Center
GSKClinicalSupportHD@gsk.com
877-379-3718
Backup
EU GSK Clinical Trials Call Center
GSKClinicalSupportHD@gsk.com
+44 (0) 20 89904466
Time Frame
Start Date: 2026-07-15
Estimated Completion Date: 2028-06-13
Participants
Target number of participants: 28
Treatments
Experimental: Depemokimab + SoC
Participants will receive depemokimab along with their existing baseline maintenance CRSwNP standard of care (SOC) treatment (excluding INCS).
Sponsors
Leads: GlaxoSmithKline

This content was sourced from clinicaltrials.gov