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NCT05764993

Prevalence of Humoral Dysfunction in Pts With Frequent Exacerbations of COPD, and the Effect of SCIgR for Prevention

Status unknown Phase 2 Last updated 15 June 2023
What this trial tests

Phase 2 trial testing CUVITRU - Ig subcutaneous human 20% in COPD Exacerbation Acute in 40 participants. Status unknown.

Timeline
1 June 2023
Primary endpoint
28 February 2025
30 December 2025

Quick facts

Lead sponsorRochester General Hospital
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment40
Start date1 June 2023
Primary completion28 February 2025
Estimated completion30 December 2025
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Rochester General Hospital

Who can join

Adults 18 to 82, any sex, with COPD Exacerbation Acute. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To examine the prevalence of humoral immunodeficiency in patients with Chronic Obstructive Pulmonary disease (COPD) by evaluating both immunoglobulin levels and vaccine responses. Patients with COPD and humoral dysfunction will be offered treatment with Subcutaneous Immune Globulin Replacement Therapy (SCIgR) in an attempt to decrease future AECOPD.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for COPD Exacerbation Acute

Currently open trials in the same condition.

Other Rochester General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05764993.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing