Afrezza Safety and Pharmacokinetics Study in Pediatric Patients

Completed · Phase 2

Conditions studied: Type 1 Diabetes Mellitus

In brief

Primary Objective: -To assess the safety and tolerability of Afrezza in children ages 4 to 17 years with type 1 diabetes mellitus (T1DM). Secondary Objectives: * To assess the ability to titrate the prandial and supplemental doses of Afrezza at each meal. * To assess pharmacokinetics (PK) following a prandial dose of Afrezza in children ages 4 to 17 years with T1DM.

Key facts

Study ID

NCT02527265

Run by

Mannkind Corporation

People needed

30

Starts

2017-09-28

Expected to finish

2020-06-25

Last updated by the study team

2021-04-06

Who can join

Age: 4 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Written or oral assent from the pediatric subject and written informed consent from the parent(s) or legal guardian and a witness, as required by both state and federal laws and the local Institutional Review Board;
• Children aged ≥4 and ≤17 years (enrolled sequentially into 3 age cohorts: 13 to 17, 8 to 12, and 4 to 7 years);
• Clinical diagnosis of T1DM and using insulin for at least 1 year;
• Currently receiving a regimen of basal/bolus insulin administered by MDI for at least 6 weeks prior to enrollment;
• Subjects with pre-breakfast self monitored blood glucose values between 80 and 250 mg/dL for 5 of 7 documented daily readings obtained in the week prior to Visit 2 (readings to be taken using glucometer provided at Screening Visit 1) and reported via the e Diary;
• Subjects on a regimen of insulin via continuous SC insulin infusion may be enrolled if they satisfy all other enrollment criteria and are willing to convert to MDI for the duration of the study, beginning 6 weeks prior to enrollment. They must continue to meet all enrollment criteria after converting to the MDI regimen;
• Total daily insulin dose ≤1.5 units/kg/day with a minimum of 3 units of RAA at every meal.
• Hemoglobin A1c (HbA1c) ≥7.0% to <10.0% at the time of screening;
• Fasting serum C-peptide ≤0.3 ng/mL;
• Forced expiratory volume in 1 second (FEV1) ≥70% of National Health and Nutrition Examination Survey (NHANES) III predicted for children ≥8 years of age or Wang predicted for children <8 years of age;
• Forced vital capacity ≥70% of NHANES III predicted for children ≥8 years of age or Wang predicted for children <8 years of age;
• Females of childbearing potential, must use "highly effective" methods of contraception throughout conduct of the trial

You may not qualify if…

• Body mass index below 25th or above 95th percentile for age and gender according to Centers for Disease Control and Prevention growth charts;
• History of physician diagnosis of asthma or any other clinically important pulmonary disease, or use of any medications to treat such conditions within the last year;
• Allergy or known hypersensitivity for AFREZZA or to drugs with similar chemical structure;
• Unstable diabetes control, defined as 2 or more episodes of severe hypoglycemia (i.e., an episode associated with a seizure, coma, or loss of consciousness) or any hospitalization or emergency room visit for poor diabetes control, ketoacidosis, hypoglycemia, or hyperglycemia within the preceding 3 months from screening;
• Serum creatinine ≥ the upper limit of normal for age;
• Respiratory tract infection within 30 days before screening or between screening and initiation of treatment period; subject may return 4 weeks after resolution of the infection for rescreening;
• Evidence of any complication of diabetes (proliferative retinopathy, autonomic neuropathy, nephropathy, etc), or likelihood of requiring laser photocoagulation, vitrectomy, or other specific treatment for diabetic retinopathy in the coming year;
• Smoking of tobacco or other substances or positive urine cotinine testing (>100 ng/mL);
• Positive urine drug screen;
• Positive urine pregnancy test for female subjects of childbearing potential;
• Inability to perform study procedures including pulmonary function testing;
• Exposure to any investigational product(s) in the past 3 months or 5 half-lives, whichever is more;
• History of eating disorder;
• Any disease or exposure to any medication which, in the judgment of the principal Investigator, may impact glucose metabolism;
• Any concurrent medical or major psychiatric condition that makes the subject unsuitable for the clinical study or impairs the subject's ability to participate in the study.
• The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Where it is running

• Children's Hospital Los Angeles — Los Angeles, California, United States
• Barbara Davis Center for Childhood Diabetes — Aurora, Colorado, United States
• Yale University Hospital — New Haven, Connecticut, United States
• University of Florida — Gainesville, Florida, United States
• USF Diabetes Center — Tampa, Florida, United States
• Atlanta Diabetes Associates — Atlanta, Georgia, United States
• Van Meter Pediatric Endocrinology, P.C. — Atlanta, Georgia, United States
• Emory University Children's Center — Atlanta, Georgia, United States
• Indiana University, Riley Hospital for Children — Indianapolis, Indiana, United States
• Barry J. Reiner, MD, LLC — Baltimore, Maryland, United States
• Diabetes, Obesity, Cardiovascular Clinical Specialists (DOCS) — Las Vegas, Nevada, United States
• Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States
• Le Bonheur Children's Hospital — Memphis, Tennessee, United States

Full record on ClinicalTrials.gov

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