The INSPIRE Trial: A Study of Interferon Gamma-1b for Idiopathic Pulmonary Fibrosis (IPF)

A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study of the Safety and Efficacy of Interferon Gamma-1b in Patients With Idiopathic Pulmonary Fibrosis (The INSPIRE Trial)

• Purpose: A phase 3, randomized, double-blind, placebo-controlled trial to determine the efficacy and safety of 200 µg of recombinant Interferon gamma-1b administered by subcutaneous (SC) injection, compared with placebo, in patients with IPF
• Enrollment: Approximately 800 patients will be enrolled from approximately 80 centers in North America and Europe
• Randomization: 2:1 active-to-placebo ratio
• Duration: at least 2 years active drug or placebo (rescue therapy will be permitted for patients who meet predefined criteria)

Study Overview

• Status: Terminated
• Conditions: Idiopathic Pulmonary Fibrosis; Pulmonary Fibrosis; Lung Disease
• Intervention / Treatment: Drug: Interferon gamma-1b ("Actimmune")

Detailed Description

INSPIRE, the largest and most comprehensive clinical trial ever conducted in IPF, has now completed enrolling patients with mild to moderate IPF. Eligible patients will receive either Interferon gamma-1b or placebo for a minimum of 2 years.

• Study Type: Interventional
• Enrollment (Actual): 826
• Phase: Phase 3

Contacts and Locations

Study Locations

• United States
  • California
    • Brisbane, California, United States, 94005
      • InterMune, Inc.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 36 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion criteria:

• Clinical symptoms consistent with IPF of >= 3 months duration
• Diagnosis of IPF within 48 months before randomization
• Age 40 through 79, inclusive
• High-resolution computed tomographic scan (HRCT) showing definite IPF. For patients with surgical lung biopsy showing definite or probable usual interstitial pneumonia (UIP), the HRCT criterion of probable IPF is sufficient.
• For patients aged < 50 years: open or video-assisted thoracoscopic (VATS) lung biopsy showing definite or probable UIP within 48 months before randomization. In addition, there are no features supporting an alternative diagnosis on transbronchial biopsy or bronchoalveolar lavage (BAL) if performed.

• For patients aged < 50 years: At least one of the following diagnostic findings, as well as the absence of any features on specimens resulting from any of these procedures that support an alternative diagnosis, within 48 months before randomization:

  • Open or VATS lung biopsy showing definite or probable UIP
  • Transbronchial biopsy showing no features to support an alternative diagnosis
  • BAL showing no features to support an alternative diagnosis IPF Disease Severity and Progression
• FVC >= 55% of predicted value (post administration of bronchodilator)
• Hemoglobin (Hb)-corrected carbon monoxide diffusing capacity/carbon monoxide transfer capacity (DLCO/TLCO) >= 35% of predicted value
• At least one of either FVC or Hb-corrected DLCO/TLCO <= 90% of predicted value

• IPF disease progression evidenced by one or more of the following within the past year and the absence of evidence of improvement in the past year:

  • Absolute decrease of >= 10% in FVC
  • Absolute decrease of >= 15% in DLCO/TLCO
  • Evidence of clinically significant worsening on chest X ray or HRCT
  • Significant worsening of dyspnea
• Distance walked >= 150 meters (492 feet) with O2 saturation >= 83% on <= 6 L/min of O2 during the 6 Minute Walk Test (6MWT) oxygen titration procedure

Exclusion criteria:

1. Not a suitable candidate for enrollment or unlikely to comply with the requirements of this study, in the opinion of the Principal Investigator (PI)
2. Forced expiratory volume in the first second (FEV1)/FVC ratio < 0.6 (after administration of bronchodilator)
3. Residual volume (RV) > 140% of predicted (before administration of bronchodilator)
4. History of clinically significant environmental exposure known to cause pulmonary fibrosis (including but not limited to drugs, asbestos, beryllium, radiation, domestic birds)
5. Known explanation for interstitial lung disease, including but not limited to radiation, sarcoidosis, hypersensitivity pneumonitis, bronchiolitis obliterans organizing pneumonia, and cancer
6. Diagnosis of any connective tissue disease, including but not limited to scleroderma, systemic lupus erythematosus, and rheumatoid arthritis
7. Clinical evidence of active infection, including but not limited to bronchitis, pneumonia, sinusitis, urinary tract infection, and cellulitis

8. On a lung transplantation waiting list at time of randomization

   Medical Exclusions:

9. Any history of malignancy likely to result in death, significant disability, or likely to require significant medical or surgical intervention within the next 3 years. This does not include minor surgical procedures for localized carcinoma (e.g., basal cell carcinoma)
10. Any condition other than IPF which, in the opinion of the PI, is likely to result in the death of the patient within the next 3 years

11. History of unstable or deteriorating cardiac, vascular, or neurologic disease within the previous 6 months, including but not limited to the following:

    • Myocardial infarction, unstable angina pectoris, coronary artery bypass surgery, or coronary angioplasty
    • Congestive heart failure requiring hospitalization
    • Uncontrolled arrhythmias
    • Thromboembolic event (e.g., deep vein thrombosis, pulmonary embolism)
    • Transient ischemic attacks (TIAs) or cerebral vascular accident
12. Any condition, which, in the opinion of the investigator, might be significantly exacerbated by the known side effects, (e.g., flu-like syndrome) associated with the administration of IFN g 1b

13. History of any of the following medical conditions:

    • Multiple sclerosis
    • Seizures within the past 10 years or taking anti seizure medication
    • Severe or poorly controlled diabetes
14. Pregnancy or lactation. Females of childbearing potential are required to have a negative serum pregnancy test before treatment and must agree to practice abstinence or prevent pregnancy by at least a barrier method of birth control for the duration of the study
15. Inability to tolerate nonsteroidal anti-inflammatory drugs (NSAIDS) or acetaminophen (paracetamol)
16. History of ethanol abuse in the past 2 years
17. Known hypersensitivity to IFN-g or closely related interferons or to any component of the study treatment

18. Presence of human immunodeficiency virus (HIV) or chronic viral hepatitis

    Laboratory Exclusions:

19. Any of the following liver function test criteria above specified limits:

    Total bilirubin > 1.5 x upper limit of normal (ULN); aspartate or alanine aminotransferases (AST/SGOT or ALT/SGPT) > 2 x ULN; alkaline phosphatase > 2 x ULN; or albumin < 3.0 mg/dL

20. Any of the following hematology test criteria outside of specified limits: WBC < 2,500/mm3, hematocrit < 30% or > 59%, platelets < 100,000 /mm3

21. Creatinine > 1.5 x ULN

    Concomitant Therapy Exclusions:

22. Prednisone therapy (prednisone or equivalent, with dose adjusted for potency) in excess of 0.125 mg/kg ideal body weight (IBW) per day or in excess of 0.25 mg/kg IBW every other day. Patients will also be excluded if they were not on a stable dose of corticosteroid therapy for at least 28 days prior to screening.
23. Prior treatment with IFN g 1b
24. Investigational therapy (i.e., agents that are not approved by local regulatory agencies) for any indication within 28 days prior to screening

25. The following therapies are excluded within 28 days prior to screening:

    • Investigational therapy for IPF, including pirfenidone
    • Any cytotoxic/immunosuppressive agent other than corticosteroids (including but not limited to azathioprine, cyclophosphamide, methotrexate, cyclosporine)
    • Any cytokine modulators (including but not limited to etanercept, infliximab)
    • Any therapy targeted to treat IPF (including but not limited to d penicillamine, colchicine, bosentan, N-acetyl-cysteine [NAC])

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Survival time from randomization to treatment completion visit, or, end of treatment period, or, last known vital status.	3.5 years

Secondary Outcome Measures

Outcome Measure	Time Frame
Lung transplant-free survival time (ongoing assessment up to end of study).	3.5 years
Total number of days without hospitalization resulting from respiratory admission diagnosis (ongoing assessment up to end of study).	3.5 years
Changes from baseline measurement to week 96 measurement in the following (measured every 24 weeks): 6-minute walk test, shortness of breath	96 weeks

Collaborators and Investigators

• Sponsor: InterMune
• Investigators: Study Chair: InterMune, Inc., Medical Information

Publications and helpful links

General Publications

• Allen RJ, Stockwell A, Oldham JM, Guillen-Guio B, Schwartz DA, Maher TM, Flores C, Noth I, Yaspan BL, Jenkins RG, Wain LV; International IPF Genetics Consortium. Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis. Thorax. 2022 Aug;77(8):829-833. doi: 10.1136/thoraxjnl-2021-218577. Epub 2022 Jun 10.
• Kreuter M, Lee JS, Tzouvelekis A, Oldham JM, Molyneaux PL, Weycker D, Atwood M, Kirchgaessler KU, Maher TM. Monocyte Count as a Prognostic Biomarker in Patients with Idiopathic Pulmonary Fibrosis. Am J Respir Crit Care Med. 2021 Jul 1;204(1):74-81. doi: 10.1164/rccm.202003-0669OC.
• Kreuter M, Lederer DJ, Molina-Molina M, Noth I, Valenzuela C, Frankenstein L, Weycker D, Atwood M, Kirchgaessler KU, Cottin V. Association of Angiotensin Modulators With the Course of Idiopathic Pulmonary Fibrosis. Chest. 2019 Oct;156(4):706-714. doi: 10.1016/j.chest.2019.04.015. Epub 2019 Apr 29.
• Cottin V, Hansell DM, Sverzellati N, Weycker D, Antoniou KM, Atwood M, Oster G, Kirchgaessler KU, Collard HR, Wells AU. Effect of Emphysema Extent on Serial Lung Function in Patients with Idiopathic Pulmonary Fibrosis. Am J Respir Crit Care Med. 2017 Nov 1;196(9):1162-1171. doi: 10.1164/rccm.201612-2492OC.
• du Bois RM, Albera C, Bradford WZ, Costabel U, Leff JA, Noble PW, Sahn SA, Valeyre D, Weycker D, King TE Jr. 6-Minute walk distance is an independent predictor of mortality in patients with idiopathic pulmonary fibrosis. Eur Respir J. 2014 May;43(5):1421-9. doi: 10.1183/09031936.00131813. Epub 2013 Dec 5.
• King TE Jr, Albera C, Bradford WZ, Costabel U, Hormel P, Lancaster L, Noble PW, Sahn SA, Szwarcberg J, Thomeer M, Valeyre D, du Bois RM; INSPIRE Study Group. Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial. Lancet. 2009 Jul 18;374(9685):222-8. doi: 10.1016/S0140-6736(09)60551-1. Epub 2009 Jun 29.

Study record dates

Study Major Dates

• Study Start: December 1, 2003
• Study Completion (Actual): May 1, 2007

Study Registration Dates

• First Submitted: January 12, 2004
• First Submitted That Met QC Criteria: January 13, 2004
• First Posted (Estimate): January 14, 2004

Study Record Updates

• Last Update Posted (Estimate): July 2, 2009
• Last Update Submitted That Met QC Criteria: July 1, 2009
• Last Verified: July 1, 2009

More Information

Terms related to this study

• Keywords: Fibrosis; Lung; Pulmonary; Interferon; Gamma; IPF; Idiopathic; Actimmune; INSPIRE; InterMune
• Additional Relevant MeSH Terms: Pathologic Processes; Respiratory Tract Diseases; Fibrosis; Lung Diseases; Pulmonary Fibrosis; Idiopathic Pulmonary Fibrosis; Anti-Infective Agents; Antiviral Agents; Antineoplastic Agents; Interferons; Interferon-gamma
• Other Study ID Numbers: GIPF-007