STOP-IPF: Saracatinib in the Treatment of Idiopathic Pulmonary Fibrosis
Study Details
Study Description
Brief Summary
Scarring of the lung, termed pulmonary fibrosis (PF), is a chronic, progressive, and usually fatal disorder. While two anti-fibrotic drugs have recently been approved for treating PF of unknown cause (idiopathic pulmonary fibrosis or IPF), neither drug is curative, and nearly 40% of patients stop taking the prescribed drug within a year because of side effects. The study includes the use of saracatinib, an investigational drug originally developed to treat certain types of cancers, in the treatment of IPF in a Phase 1b/2a clinical trial.
The objectives of this study are to: i) evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics, and to explore the efficacy of saracatinib in IPF; ii) identify biomarkers of Src kinase activity and fibrogenesis linked to pulmonary fibrosis; and iii) explore the application of these biomarkers to assess the anti-fibrotic effect of saracatinib in IPF patients
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1/Phase 2 |
Detailed Description
This is a double blind, randomized, placebo-controlled, single-dose, three-site trial. The trial is a biomarker-based, integrated Phase 1b/2a clinical trial involving 100 subjects. One group (n=50) will receive placebo, while the other group (n=50) will receive 125 mg of oral saracatinib once daily.
Randomization will be stratified by center. The randomization scheme will be in random blocks of 2 and 4 within each stratum to maintain balance. The study is designed to have interim analysis of the drop-out rates when approximately 30% of the randomized patients have achieved the 24-week assessment. Should the drop-out rate be higher than the 20% that is anticipated, a new sample size calculation will be performed to make sure that the power of the study is maintained at 80% .
Duration of follow-up will be 28 weeks including 24 weeks of treatment with saracatinib or placebo.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Saracatinab saracatinib 125 mg once daily by mouth for 24 weeks |
Drug: Saracatinab
125 mg once daily by mouth for 24 weeks
|
| Placebo Comparator: Placebo matching placebo once daily by mouth for 24 weeks |
Drug: Placebo
once daily by mouth for 24 weeks
|
Outcome Measures
Primary Outcome Measures
- Safety of saracatinib in IPF as measured by frequency of adverse events [24 weeks]
Safety data will be listed and summarized with patient counts and percentages in each treatment arm
- Tolerability of saracatinib in IPF as measured by Severity of adverse events [24 weeks]
A listing of all adverse eventsw by patient will be presented. This listing will include patient number, adverse event (actual term and preferred term), event stand and end dates, CTCAE grade, relationship to the study drug/procedure, seriousness and outcome. A listing of SAEs will be produced using the similar format. This is not a scale. It is a data capture tool.
- Pharmacokinetics of saracatinib in IPF as measured by serum levels [24 weeks]
Serum levels of saracatinib
- Pharmacodynamics of saracatinib in IPF as measured by change in serum β-CTX [24 weeks]
Change in serum β-CTX as a Src kinase dependent biomarker
- Efficacy of saracatinib in IPF as measured by change in FVC [24 weeks]
Change in FVC from baseline
Secondary Outcome Measures
- Efficacy of saracatinib in IPF (HRCT) [24 weeks]
Change in HRCT quantitative analysis of the extent of pulmonary fibrosis. The analysis pf HRCT data will involve data-driven texture analysis (DTA), a machine learning method capable of automatic detection and quantification of lung fibrosis on HRCT
- Efficacy of saracatinib in IPF (DLCO) as measured by change in DLCO [24 weeks]
Change in diffusing capacity of the lung for carbon monoxide (DLCO)
- Efficacy of saracatinib in IPF (exacerbations) as measured in time to first acute exacerbation [24 weeks]
Time to the first acute exacerbation
- Efficacy of saracatinib in quality of life in IPF (SGRQ) as measured by total score on SGRQ questionnaire [24 weeks]
Total score on the SGRQ questionnaire. St. George's Respiratory Questionnaire (SGRQ) is a 50-item, self-administered, respiratory-specific questionnaire with items covering three domains: symptoms, activities, impacts. Each domain and a total score range from 0-100, with higher scores connoting greater impairment.
- Efficacy of saracatinib in quality of life in IPF (L-IPF) as measured by total score on L-IPF questionnaire [24 weeks]
Total score on the L-IPF questionnaire. Living with IPF (L-IPF) is an IPF-specific questionnaire whose 43 items cover two modules: symptoms and impacts. A model-based scoring algorithm has been developed via psychometric methods.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
IPF of any duration, confirmed or diagnosed by ILD center or expert according to Fleischner Guidelines (33)
-
Women or men >40 years of age at the time of screening
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FVC%>45% of predicted value (GLI-2012)
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Single breath DLCO% 30 - 79 inclusive of predicted (without bronchodilator and uncorrected for hemoglobin)
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FEV1/FVC>70 (GLI-2012)
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Provision of signed/dated written informed consent prior to any study-specific procedures
-
Females must be of nonchildbearing potential (defined as surgically sterilized [ie, bilateral tubal ligation, bilateral oophorectomy or complete hysterectomy] or postmenopausal [defined as 12 months with no menses without an alternative medical cause] with a follicle-stimulating hormone [FSH] > 25.8 IU/L) or use a highly effective method of contraception (defined as combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation; progestogen only hormonal contraception associated with inhibition of ovulation; intrauterine device (IUD); intrauterine hormone-releasing system (IUS) for the duration of the study (from the time they sign consent) and for 3 months after the last dose of drug/matching placebo
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Male subjects must be surgically sterile or using an acceptable method of contraception (defined as barrier methods in conjunction with spermicides) for the duration of the study (fr om the time they sign consent) and for 3 months after the last dose of drug/matching placebo to prevent pregnancy in a partner. Male subjects must not donate or bank sperm for the duration of the study (from the time they sign consent) and for 3 months after the last dose of drug/matching placebo.
Exclusion Criteria:
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Requirement for supplemental oxygen > 4 L/min at rest to maintain saturation > 90%
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Active infection at screening or randomization
-
Known active or latent hepatitis B or C
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Life expectancy for disease other than IPF < 2.5 years (Investigator assessment)
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Listed for lung transplantation
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Taking pirfenidone or nintedanib in the last 4 weeks
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Pregnancy or lactation
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Known allergic reactions to components of saracatinib
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Treatment with another investigational drug or other intervention within 8 weeks
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Current smoker or tobacco use within 4 months
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Major surgery within the past 2 months
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Advanced hematologic, renal, hepatic, any lung disease determined by the investigator to be non-IPF related or metabolic disease that, in the opinion of the investigator, would make it unsafe for the person to receive study drug.
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Previous lung transplantation
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Inability to attend scheduled study visits
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Inability to give informed consent
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Inability to perform pulmonary function testing
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History of malignancy in the past two years, other than squamous or basal cell skin cancer
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Previous acute exacerbation of IPF requiring hospitalization and/or antibiotics within 90 days before the first dose of the investigational product
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Liver function test results ≥3× upper limit of normal (ULN) liver isoform of aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma glutamyl transpeptidase (GGT), or alkaline phosphatase (ALP) or ≥2×ULN total bilirubin (excepting documentation of benign hereditary cause). An isolated total bilibrubin elevation (ie, no significant concomitant elevation in ALT or AST) at baseline of ≤ 2xULN is permitted. If there is concomitant elevation in ALT or AST to ≤3xULN, then the threshold for total bilirubrin is ≤1.5xULN.
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Creatinine clearance <30 mL/min calculated by Cockcroft-Gault formula
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Known pulmonary hypertension (PH) requiring PH-specific treatment
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Chronic oral corticosteroids at doses greater than prednisone 10 mg/day (or equivalent)
-
Refer to 6.5 Concomitant Therapy for exclusions based on co-medications
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | National Jewish Health | Denver | Colorado | United States | 80206 |
| 2 | Yale University School of Medicine | New Haven | Connecticut | United States | 06510 |
| 3 | Icahn School of Medicine at Mount Sinai | New York | New York | United States | 10029 |
| 4 | Baylor Scott & White Research Institute | Dallas | Texas | United States | 75246 |
Sponsors and Collaborators
- National Jewish Health
- Yale University
- Icahn School of Medicine at Mount Sinai
- AstraZeneca
- National Center for Advancing Translational Science (NCATS)
Investigators
- Principal Investigator: Gregory Downey, MD, National Jewish Health
- Principal Investigator: Annetine C Gelijns, PhD, Icahn School of Medicine at Mount Sinai
- Principal Investigator: Naftali Kaminski, MD, Yale University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 5UH3TR002445
- UG3TR002445