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Safety Study of Zileuton Injection in Patients With Asthma

Information source: Critical Therapeutics
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Asthma

Intervention: Zileuton injection (Drug)

Phase: Phase 1/Phase 2

Status: Completed

Sponsored by: Critical Therapeutics

Official(s) and/or principal investigator(s):
Dana Hilt, MD, Study Director, Affiliation: Critical Therapeutics Incorporated


The prevalence of asthma continues to increase. Despite the large number of available therapies, many patients continue to require emergency deparment (ED) visits and intensive therapy. However, ED visits continue to be a major contributor to the healthcare cost of asthma treatment. In the United States alone, asthma is the 11th most common reason for ED visits, with ED visits and hospitalizations accounting for almost 50% of the healthcare cost for asthma. Additionally, while only 20% of asthmatics have had ED visits or hospitalizations, these patients account for over 80% of the direct costs for asthma treatment. Current National Asthma Education and Prevention Program (NAEPP) guidelines regarding management of acute asthma exacerbations in the ED setting include: oxygenation for most patients, inhaled short-acting β2-agonists and systemic corticosteroids. Zileuton, a specific 5-lipoxygenase inhibitor, has been extensively studied in inflammatory diseases such as asthma, which involve leukotrienes as mediators of inflammation. Zileuton Immediate Release (IR) tablets (Zyflo®) were approved by the Food and Drug Administration (FDA) in December 1996 for the prevention and treatment of asthma in adults and children 12 years of age and older. The results of the 2 pivotal studies in asthmatics with zileuton IR tablets demonstrated that zileuton at a dose of 600 mg QID produced and maintained a lasting improvement of lung function. In addition to the lasting effect of zileuton, an acute bronchodilation (as early as 60 minutes) was observed after administration of the first 600 mg oral dose. This acute bronchodilator effect may benefit patients during an acute exacerbation of asthma when added to the usual care in the ED or clinic setting. Critical Therapeutics has developed an injectable formulation of zileuton that will be explored for use in acute asthma exacerbations. This initial study is intended to provide PK data, information on safety and tolerability and some indication of pharmacologic activity as evidenced by lung function changes. In an attempt to enhance the potential for observing effects on lung function, only those patients with a demonstrated ability to respond by an increase in FEV1 of at least 10% within 3 hours after oral zileuton dosing will be enrolled.

Clinical Details

Official title: Assessment of Safety, Tolerability, and Pharmacokinetics of Zileuton Injection in Patients With Asthma

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Primary outcome:

Clinical laboratory tests through 48 hours post-injection

Vital signs through 10 hours post-injection

Pulse oximetry through 10 hours post-injection

Injection site evaluations through 10 hours post-injection

Adverse event assessments through 48 hours post-injection

Blood samples for PK through 10 hours post-injection

Secondary outcome:

Spirometry through 10 hours post-injection

Peak expiratory flow rates through 20 min. post-injection


Minimum age: 12 Years. Maximum age: N/A. Gender(s): Both.


Inclusion Criteria:

- Diagnosis of asthma

- Morning FEV1 of 40-80% of predicted normal

- Evidence post-bronchodilator increase in FEV1 of at least 15%

- Evidence of at least 10% increase in FEV1 within 3 hours after oral 600 mg zileuton


- Signed IRB approved informed consent

- Patients must be willing and able to withhold:

- short acting β2-agonists for at least 6 hours prior to spirometry

- inhaled corticosteroids (ICS) for at least 24 hours prior to sprirometry

- long acting β2-agonists (LABA) for 7 days and be willing and able to switch from a

LABA/ICS combination product to a monotherapy ICS product Exclusion Criteria:

- Females of childbearing potential not using effective contracception

- Any uncontrolled systemic disease other than asthma

- Patient with known hypersensitivity to zileuton IR tablets or zileuton injection or

any of the components found therein

- An upper or lower respiratory tract infection within 2 weeks of screening

- An ED visit or hospitalization for asthma within 3 months of screening

- Oral or parenteral corticosteroid use for asthma exacerbation within 3 months of


- Current cigarette smoker and/or >10 pack-year smoking history

- History of hepatitis B (HBV) or hepatitis C infection or other active liver disease

or chronic hepatitis

- Screening ALT >1. 5x ULN

- Patient with impaired renal function or serum creatinine >1. 5x ULN

- History of HIV infection

- History of drug or alcohol abuse within 1 year of screening

- Patient taking any of the following asthma/allergy medications:

- Anti-IgE meds within 3 months of screening

- Zileuton IR tablets within 1 month of screening

- Inhaled or oral steroids not stable for at least 1 month

- Theophylline, cromolyn, or nedocromil within 7 days of screening

- Leukotriene receptor agonists within 7 days of screening

- Warfarin, propranolol, inhaled or sytemic anticholinergics within 7 days of screening

- Long acting beta agonist within 7 days of screening

- Oral beta-2 agonists within 12 hours of screening

- Immunotherapy injections not in a stable dosing phase

- Female patient who is pregnant or breast-feeding or plans to become pregnant during

the study period

- Participation in another research study within 30 days of screening

- Patient is the Investigator or other staff or relative who is directly involved in

the conduct of the study

Locations and Contacts

Allergy & Asthma Specialist Medical Group, Huntington Beach, California 92647, United States

Allergy and Asthma Medical Group and Research Center, San Diego, California 92123, United States

Colorado Allergy and Asthma Centers, PC, Englewood, Colorado 80112, United States

Northeast Medical Research Associates, North Dartmouth, Massachusetts 02747, United States

Clinical Research Institute, Minneapolis, Minnesota 55402, United States

The Clinical Research Center, L.L.C., St. Louis, Missouri 63141, United States

Princeton Center for Clinical Research, Skillman, New Jersey 08558, United States

Bernstein Clinical Research Center, Cincinnati, Ohio 45231, United States

Allergy Associates Research Center, Portland, Oregon 97213, United States

Western Sky Medical Research, El Paso, Texas 79902, United States

Additional Information

Related publications:

Fuhlbrigge AL, Adams RJ, Guilbert TW, Grant E, Lozano P, Janson SL, Martinez F, Weiss KB, Weiss ST. The burden of asthma in the United States: level and distribution are dependent on interpretation of the national asthma education and prevention program guidelines. Am J Respir Crit Care Med. 2002 Oct 15;166(8):1044-9.

Colice GL, Burgt JV, Song J, Stampone P, Thompson PJ. Categorizing asthma severity. Am J Respir Crit Care Med. 1999 Dec;160(6):1962-7.

Rodrigo GJ, Rodrigo C, Hall JB. Acute asthma in adults: a review. Chest. 2004 Mar;125(3):1081-102. Review.

Starting date: January 2006
Last updated: September 24, 2007

Page last updated: August 23, 2015

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