Clinical Trials
Aeris is conducting clinical studies evaluating the Aeris Biologic Lung Volume System in phase II studies. The goal of the studies is to assess the safety and efficacy of the BLVR system using different treatment doses in patients with advanced homogeneous or upper lobe emphysema that is not responsive to medical therapy. All patients that meet the study inclusion / exclusion criteria and choose to participate receive the BLVR treatment.
Further information regarding clinical studies sponsored by Aeris may be found at www.clinicaltrials.gov; enter “Aeris” in the “Search Clinical Trials” box.
Participation Criteria for Aeris BLVR Clinical Trial
Criteria for participation in this trial include:
· ≥ 40 years of age
· Advanced homogeneous or upper lobe predominant emphysema that is disabling despite medical therapy
· Able to tolerate bronchoscopy
· Have not smoked for 4 months prior to and during study participation
· Have not had previous surgical procedures of the lung
· Have not had clinically significant asthma, chronic bronchitis, or bronchiectasis
Patients who believe they meet these participation criteria and are interested in learning more about the BLVR clinical trial, should review the Participating Sites for a BLVR clinical trial site near their home, and should contact the Site’s Study Coordinator.
Participating Sites – Aeris BLVR Clinical Trial
Active Sites:
UNITED STATES
Alabama
University of Alabama, Birmingham
Dr. Mark Dransfield – Principal Investigator
Study Coordinator: Sherry Tidwell (205-996-6602)
Stidwell@uab.edu
Arizona Pulmonary Associates, Phoenix
Dr. Mark Gotfried – Principal Investigator
Study Coordinator: Dr. Li Yi Fu (602-258-4951)
palyf@aol.com
Iowa
University of Iowa Hospitals and Clinics, Iowa City
Dr. Geoffrey McLennan – Principal Investigator
Study Coordinator: Kim Sprenger (319-353-8862)
kimberly-sprenger@uiowa.edu
Kansas
Veritas Clinical Specialties, Ltd., Topeka
Dr. William Leeds – Principal Investigator
Study Coordinator: Suzanne Nicklin (785-354-0735)
snicklin@verispecial.com
Maryland
St. Joseph’s Medical Center, Towson
Dr. Mark Krasna – Principal Investigator
Study Coordinator: Pat Johnson (410-337-4569)
patriciajohnson@catholichealth.net
Ohio
Akron General Medical Center, Akron
Dr. Sanjiv Tewari – Principal Investigator
Study Coordinator: Debbie Hudock (330-344-1570)
dhudock@agmc.org
Cleveland Clinic, Cleveland
Dr. Thomas Gildea – Principal Investigator
Study Coordinator: Yvonne Meli (216-445-4215)
meliy@ccf.org
Pennsylvania
Temple University, Philadelphia
Dr. Gerard Criner – Principal Investigator
Study Coordinator: Gayle Jones (215-707-4917)
JonesGM@tuhs.temple.edu
South Carolina Medical University of South Carolina Hospital, Charleston
Dr. Charlie Strange – Principal Investigator
Study Coordinator: Ester Cummings (843-792-6890)
cumminew@musc.edu
ISREAL
Rabin Medical Center
Belinson Hospital
Petach Tivka, 49100
Yael Refaely, MD - Principal Investigator
Study Coordinator: Avital Yacobi (972-3-937-6707)
avitaly@clalit.org.il
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