Comparing Two Pneumococcal Vaccines in Adults With Chronic Obstructive Pulmonary Disease (PNEUMO)

University of Minnesota (UMN)

Status and phase

Completed

Phase 3

Conditions

Pulmonary Disease, Chronic Obstructive

Treatments

Biological: Prevnar (PCV7)

Biological: Pneumovax (PPSV23)

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT00457977

477

U10HL074424 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Pneumococcal disease is a serious bacterial infection that can affect different parts of the body, including the lungs. People with chronic illnesses, such as chronic obstructive pulmonary disease (COPD), have a greater risk of developing pneumonia and meningitis as a result of pneumococcal disease. This study will compare the immune response to two types of pneumococcal vaccines in adults with COPD.

Full description

Individuals who are infected with the Streptococcus pneumoniae bacteria may develop pneumococcal disease, a serious disease that kills more people in the United States than all other vaccine-preventable diseases combined. Individuals with COPD, characterized by breathing difficulties due to damaged and obstructed lung airways, may have an increased risk of developing serious complications from pneumococcal disease, including pneumonia and meningitis. Currently, there are two types of pneumococcal vaccines available. The pneumococcal capsular polysaccharide (CPS) vaccine, known as Pneumovax, is typically given to adults 65 years of age or older and to any individuals with a serious health condition, including heart disease, lung disease, and diabetes. The diphtheria protein-conjugated vaccine (PCV7), known as Prevnar, is typically given to infants; however, adults who receive this vaccine may also have a favorable response. The purpose of this study is to compare the immune response to the Pneumovax and Prevnar vaccines in adults with COPD.

This study will enroll adults with mild to moderate COPD. Participants will be randomly assigned to receive either the Pneumovax or Prevnar vaccine. This will involve one or two injections. Blood collection will occur during study visits at Months 1, 12, and 24. Study researchers will contact participants by telephone at Months 6 and 18 to document any pneumococcal infections and any additional pneumococcal vaccinations.

Enrollment

181 patients

Sex

All

Ages

40+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Diagnosis of Chronic Obstructive Pulmonary Disease (COPD)
Post-bronchodilator forced expiratory volume at one second

/forced vital capacity (FEV1/FVC) level less than 70%
Ten or more pack-years of smoking
Willing to make return visits to the study clinic and accept telephone contact
Last pneumococcal vaccination occured at least 5 years prior to study entry

Exclusion criteria

Asthma
Sensitivity to pneumococcal vaccine
Known bleeding disorder, or requires long-term anticoagulation therapy
Presence of chronic disease that may impair pneumococcal vaccine response
Acute illness requiring antibiotics in the month prior to study entry
Medical condition that makes survival for 24 months following study entry unlikely
Pregnant