Summary

Eligibility
for people ages 10-17 (full criteria)
Location
at UCSF
Dates
study started
study ends around
Principal Investigator
by Laya Ekhlaspour, MD (ucsf)
Headshot of Laya Ekhlaspour
Laya Ekhlaspour

Description

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 10 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.

Official Title

INHALE-1st: Technosphere Insulin (Afrezza®) In Combination With Basal Insulin For Youth With Newly-Diagnosed Type 1 Diabetes

Keywords

Type 1 Diabetes Mellitus, Diabetes Mellitus, Insulin, Inhaled, Afrezza, Technosphere, Pediatric, Inhaled Insulin, Type 1 Diabetes, Newly diagnosed type 1 diabetes, Technosphere Insulin, rapid-acting inhaled insulin, Meal-time inhaled insulin, Insulin Resistance, Respiratory Aspiration, Basal insulin, Afrezza (Technosphere Insulin) + Basal Insulin

Eligibility

You can join if…

Open to people ages 10-17

  • Age 10 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 10 days following T1D diagnosis (day 1 is based on the first insulin injection) if not hospitalized with diabetic ketoacidosis (DKA) and within 10 days of hospital discharge if hospitalized with DKA
  • 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

You CAN'T join if...

  • Prior insulin treatment for stage 2 T1D
  • 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) in the judgment of the investigator
  • 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

Locations

  • University of California San Francisco not yet accepting patients
    San Francisco California 94158 United States
  • Children's Hospital Los Angeles not yet accepting patients
    Los Angeles California 90027 United States
  • Barbara Davis Center for Diabetes Young Adult Clinic accepting new patients
    Aurora Colorado 80045 United States
  • Joslin Diabetes Center accepting new patients
    Boston Massachusetts 02215 United States

Lead Scientist at University of California Health

  • Laya Ekhlaspour, MD (ucsf)
    I am a physician-scientist and an assistant Professor of Pediatrics at the University of California, San Francisco, and my research is focused on the use of technology in children with type 1 diabetes.

Details

Status
accepting new patients at some sites,
but this study is not currently recruiting here
Start Date
Completion Date
(estimated)
Sponsor
Mannkind Corporation
ID
NCT07224321
Phase
Phase 2 research study
Study Type
Interventional
Participants
Expecting 100 study participants
Last Updated