Phase I Study Evaluating the Safety and Pharmacokinetics of Budesonide, Glycopyrronium, and Formoterol Fumarate Inhalation Aerosol (BGF MDI) in Healthy Volunteers

Completed · Phase 1

Conditions studied: Healthy Volunteers

In brief

This is a Phase I, Randomized, Double-Blind Within Device, Single-Dose, Four-Period, Six-Treatment, Cross-Over Study Evaluating the Safety and Pharmacokinetics of Three Doses of Budesonide, Glycopyrronium, and Formoterol Fumarate Inhalation Aerosol (BGF MDI), One Dose of Glycopyrronium and Formoterol Fumarate Inhalation Aerosol (GFF MDI), and Two Doses of Symbicort® Inhalation Aerosol in Healthy Volunteers. The primary objective of the study is to determine a dose of budesonide that when formulated with glycopyrronium and formoterol fumarate in BGF MDI provides comparable systemic exposure \[pharmacokinetics (PK)\] to budesonide following administration of Symbicort MDI.

Key facts

Study ID

NCT01980615

Run by

Pearl Therapeutics, Inc.

People needed

84

Starts

2013-11-01

Expected to finish

2013-12-01

Last updated by the study team

2014-04-14

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Provide signed written informed consent form
• 18 and 45 years (inclusive)
• Healthy subject confirmed by a thorough medical history and physical examination, ECG, vital signs and clinical laboratory tests
• Females of childbearing potential and males with female partners of childbearing potential must agree to use medically acceptable contraception
• Body mass index (BMI) between 18.5 and 32 kg/m2 (inclusive) and a minimum weight of 50 kg at the screening visit
• Results of complete laboratory analyses should be within the normal range or determined to be not clinically significant by the Investigator

You may not qualify if…

• Pregnancy, nursing female subjects, or subjects trying to conceive
• Clinically significant medical conditions
• History of ECG abnormalities
• Symptomatic prostatic hypertrophy, bladder neck obstruction, or urinary retention
• Known diagnosis of glaucoma
• Known or suspected history of substance-related disorders within 1 year of screening
• Treatment with an investigational drug within 30 days or five half-lives (whichever is longer) prior to screening period
• Hypersensitivity to lactose or any drug or component of the formulation(s) used in this study
• Positive screen for human immunodeficiency virus (HIV), hepatitis B surface antigen (HbsAg) or positive hepatitis C antibody at screening.
• Major surgery within four weeks or minor surgery within 2 weeks of drug administration
• Any other condition and/or situation that causes the Investigator to deem a subject unsuitable for study participation

Where it is running

• Pearl Therapeutics Study Site — Baltimore, Maryland, United States

Full record on ClinicalTrials.gov

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