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Study of the AeriSeal System for HyPerInflation Reduction in Emphysema (ASPIRE)

A

Aeris Therapeutics

Status and phase

Terminated
Phase 3

Conditions

Pulmonary Emphysema

Treatments

Other: Optimal Medical Therapy
Device: Treatment plus Optimal Medical Therapy

Study type

Interventional

Funder types

Industry

Identifiers

NCT01449292
03-C11-003PLV

Details and patient eligibility

About

The purpose of this study is to demonstrate the safety and efficacy of AeriSeal System treatment plus optimal medical therapy compared in patients with advanced upper lobe predominant (ULP) heterogeneous emphysema.

Enrollment

300 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Willing and able to provide informed consent

  2. Age ≥ 40 years

  3. On optimal medical therapy* for more than 1 month

  4. Advanced upper lobe predominant emphysema confirmed by CT scan

  5. Two (2) subsegments appropriate for treatment in 2 different upper lobe segments in each lung based upon CT scan (total 4 available subsegments)

  6. MRCD score of ≥ 2 post pulmonary rehab (using modified MRCD scale of 0-4)

  7. 6MWT distance ≥ 150 m post pulmonary rehab

  8. Spirometry 15 minutes after administration of a bronchodilator showing BOTH:

    1. FEV1 < 50% predicted
    2. FEV1/FVC ratio < 70%
  9. Plethysmographic lung volumes showing BOTH:

    1. TLC > 100% predicted
    2. RV > 150% predicted
  10. DLco ≥ 20% and ≤ 60% predicted

  11. Blood gases and oxygen saturation showing BOTH:

    1. SpO2 ≥ 90% on ≤ 4 L/min supplemental O2
    2. PaCO2 < 65 torr
  12. Smoking history of ≥ 20 pack-years with abstinence for 16 weeks

Exclusion criteria

  1. Prior lung volume reduction surgery, lobectomy or pneumonectomy, or lung transplantation

  2. Requirement for ventilator support (other than CPAP or BPAP for sleep apnea)

  3. Three (3) or more COPD exacerbations requiring hospitalization within 1 year of Screening visit or a COPD exacerbation requiring hospitalization within 8 weeks

  4. Use of systemic steroids > 20 mg/day or equivalent immunosuppressive agents, heparins, oral anticoagulants or investigational medications

    Exclusion Criteria (continued):

  5. a-1 antitrypsin serum level of < 80 mg/dL (immunodiffusion) or < 11 µmol/L (nephelometry)

  6. CT scan: Presence of any of the following radiologic abnormalities:

    1. Pulmonary nodule on CT scan greater than 1.0 cm in diameter
    2. Radiologic picture consistent with active pulmonary infection
    3. Significant interstitial lung disease
    4. Significant pleural disease
    5. Giant bullous disease
  7. Clinically significant asthma

  8. Clinically significant bronchiectasis

  9. Pulmonary hypertension

  10. Allergy or sensitivity to medications required to safely perform AeriSeal System treatment under general anesthesia or conscious (moderate procedural) sedation

  11. Participation in an investigational study of a drug, biologic, or device not currently approved for marketing

  12. Body mass index < 15 kg/m2 or > 35 kg/m2

  13. Female patient pregnant or breast-feeding or planning to be pregnant in the next year

  14. Any abnormal screening laboratory test result

  15. Significant comorbidity including any of the following:

    1. HIV/AIDs
    2. Active malignancy
    3. Stroke or TIA within 12 months
    4. Myocardial infarction within 12 months
    5. Congestive heart failure within 12 months
  16. Any condition that would interfere with the intent of the study or would make participation not in the best interest of the patient such as alcoholism, high risk for drug abuse or noncompliance in returning for follow-up visits

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups

Treatment plus Optimal Medical Therapy
Experimental group
Description:
Patients will be treated with the AeriSeal System and Optimal Medical Therapy
Treatment:
Device: Treatment plus Optimal Medical Therapy
Optimal Medical Therapy
Active Comparator group
Description:
Patients will be treated according to Optimal Medical Therapy
Treatment:
Other: Optimal Medical Therapy

Trial contacts and locations

40

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Data sourced from clinicaltrials.gov

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