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Clinical trialNCT00515164CompletedPhase 2Interventional

US Biologic Lung Volume Reduction (BLVR) Phase 2 Emphysema Study

SponsorAeris TherapeuticsEnrollment22Chronic Obstructive Pulmonary DiseasePulmonary Emphysema
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study it to evaluate the efficacy and safety of the 20 mL BLVR System in patients with advanced upper lobe predominant emphysema.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

8 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Pulmonary Associates

    Phoenix, Arizona, United States

  • University of Iowa Hospitals & Clinics

    Iowa City, Iowa, United States

  • Veritas Clinical Specialties, Ltd

    Topeka, Kansas, United States

  • St Joseph'S Medical Center

    Towson, Maryland, United States

  • Akron Medical Center

    Akron, Ohio, United States

  • Pulmonary, Allergy & Critical Care Medicine, Cleveland Clinic Foundation

    Cleveland, Ohio, United States

  • Temple University Lung Center

    Philadelphia, Pennsylvania, United States

  • Medical University of South Carolina

    Charleston, South Carolina, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Biologic Lung Volume Reduction - 20 mL Hydrogel
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Aug 2007
Primary completion
30 Apr 2008
Completion
31 Dec 2009
Last update posted
24 Oct 2011
Registered enrollment
22
Registry id
NCT00515164

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.