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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

 

Aeris Therapeutics, Inc.
10K Gill Street
Woburn, MA 01801
Tel: 781.937.0110
Fax: 781.937.0077