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Clinical Trials in the USA / NCT07224321
Recruiting Phase 2

INHALE-1st: Afrezza® For Youth With Newly-Diagnosed Type 1 Diabetes

NCT07224321 · tracked via the Priya Life Science USA tracker
Sponsor
Mannkind Corporation
Phase
Phase 2
Started
2026-02-04
Last updated
2026-08-13

Condition(s) studied

Type 1 Diabetes Mellitus

Investigational drug(s) / intervention(s)

Technosphere InsulinTechnosphere InsulinBasal insulin

Technosphere Insulin: 2 unit

Technosphere Insulin: 4, 8, 12 units

Basal insulin: subcutaneously-injected basal insulin

Study summary

INHALE-1st is a Phase 2, single-arm, multi-center, clinical study evaluating the safety and efficacy of Afrezza in combination with subcutaneously-injected basal insulin (BI) for youth 6 to \<18 years old with newly diagnosed stage 3 type 1 diabetes (T1D). The study will also evaluate the effect of an Afrezza plus BI reigmen on participant and parent/legally authorized representative satisfaction. Participants will be followed for 13 weeks during the main phase followed by an optional Extension Phase for participants continuing to use Afrezza in combination with BI for up to 26 weeks.

Eligibility

Sex
ALL
Min age
6 Years
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria: * Age 6 to \<18 years of age * Clinical diagnosis of stage 3 T1D, per the investigator. Stage 3 is defined as hyperglycemia, meeting ADA glycemic and clinical diagnostic criteria * Able to start the Afrezza-BI regimen within 21 days following T1D diagnosis (day 1 is based on the first insulin dose) * Forced Expiratory Volume in One Second (FEV1) \>80.0% of predicted Global Lung Function Initiative (GLI) value * Investigator believes that participant can be expected to follow the study protocol * No medical, psychiatric, psychosocial conditions, or medications being taken that in the investigator's judgment would be a safety concern for participation in the study Exclusion Criteria: * Prior insulin treatment for stage 2 T1D * In the judgment of the investigator, history of chronic lung disease, such as asthma, or chronic obstructive pulmonary disease, lung cancer, or any other clinically important pulmonary disease (e.g., cystic fibrosis, bronchopulmonary dysplasia) * Allergy or known hypersensitivity to human regular insulin * Smoking (includes cigarettes, cigars, pipes, marijuana, and vaping devices) within 3 months prior to screening and/or positive cotinine test for smoking * Positive urine pregnancy test for female subjects of childbearing potential

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Children's Hospital Los Angeles Los Angeles California Recruiting
University of California San Francisco San Francisco California Recruiting
Barbara Davis Center for Diabetes Young Adult Clinic Aurora Colorado Recruiting
Yale University New Haven Connecticut Recruiting
University of Florida Gainsville Florida Recruiting
Indiana University Indianapolis Indiana Recruiting
Joslin Diabetes Center Boston Massachusetts Recruiting
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma Recruiting
Baylor College of Medicine Houston Texas Recruiting
University of Virginia Charlottesville Virginia Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07224321 on ClinicalTrials.gov ↗ ← All trials in the USA