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Completed

NCT Number: NCT00347659

US 10 mL Biologic Lung Volume Reduction (BLVR) Phase 1 Emphysema Study

The purpose of this study is to evaluate the safety of the Biologic Lung Volume Reduction System (BLVR) for patients with advanced emphysema.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Caritas St. Elizabeth's Medical Center, Boston, Massachusetts, United States

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About this study

Emphysema is a progressive, debilitating disease that affects nearly 3 million people in the United States or roughly one percent of the US population. The disease is characterized by destruction of lung tissue as a result of inflammation caused by exposure to noxious inhaled agents for extended periods. The most common cause of this condition is cigarette smoking, although genetic and occupational causes account for up to 10% of cases. Despite aggressive public health initiatives aimed at discouraging the use of cigarettes, smoking-related lung diseases remain a significant cause of disability and death in the United States. Currently there are 46 million smokers in the US. Due to the number of current and new smokers, emphysema is expected to remain a leading cause of morbidity and mortality in the United States for years to come.

Aeris has developed a novel bronchoscopic system for achieving the benefits of lung volume reduction without surgery. The Biologic Lung Volume Reduction (BLVR) System, a new investigational therapy for emphysema, is intended to reduce lung volume over a period of weeks by collapsing and promoting the remodeling of diseased areas of the lung. The resulting reduction in lung volume is intended to restore a more normal physiological relationship between lung and chest wall, improve breathing and exercise capacity and alleviate symptoms of chronic dyspnea. This study will evaluate the safety of the BLVR System in patients with advanced emphysema.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of advanced heterogeneous emphysema
  • Age >/= 40
  • Clinically significant dyspnea
  • Failure of standard medical therapy to relieve symptoms
  • Pulmonary function tests with protocol-specified ranges

Exclusion criteria

  • Alpha-1 protease inhibitor deficiency
  • Tobacco use within 16 weeks of initial clinic visit
  • Body mass index < 15 kg/m2 or > 35 kg/m@
  • Clinically significant asthma, chronic bronchitis or bronchiectasis
  • Allergy or sensitivity to tetracycline
  • Prior lung volume reduction surgery, prior lobectomy or pneumonectomy, prior lung transplantation, prior endobronchial valve placement, prior airway stent placement or prior pleurodesis

Treatment and study plan

BLVR System

Drug

Treatment is administered in a single treatment session.

Primary outcomes

  1. SAEs - Safety of the procedure from initiation of treatment through hospital discharge.

    Time frame: 1 week post treatment

  2. SAEs - Safety of the treatment through Week 12.

    Time frame: 12 weeks post procedure

Secondary outcomes

  1. SAEs - Safety of the treatment through Week 48.

    Time frame: 48 weeks post treatment

  2. Evaluation of radiologic changes.

    Time frame: 12 weeks post treatment

  3. Improvement in exercise capacity.

    Time frame: 12 weeks post treatment

  4. Improvement in quality of life.

    Time frame: 12 weeks post treatment

  5. Decrease in trapped gas.

    Time frame: 12 weeks post treatment

  6. Improvement in lung function.

    Time frame: 12 weeks post trreatment

  7. Improvement in symptoms.

    Time frame: 12 weeks post treatment

Sponsors and collaborators

Lead sponsor

Aeris Therapeutics

Industry

Registry information

Official study title

Phase 1 Study of the Biologic Lung Volume Reduction (BLVR) System in Patients With Advanced Upper Lobe Predominant Emphysema

Important dates

Study start
2006
Primary completion
2006
Study completion
2007
First posted
Jul 4, 2006
Registry last updated
Mar 6, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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