MannKind to Showcase Pediatric and Adult Afrezza Data at ATTD 2026

  • MannKind to present new Afrezza data at ATTD 2026, including pediatric and adult studies.
  • FDA review for Afrezza pediatric indication set for May 29, 2026.
  • INHALE-1 study highlights dosing and titration patterns in pediatric patients.
  • Afrezza is the only ultra-rapid-acting inhaled insulin approved for adults with diabetes.

MannKind's presentation at ATTD 2026 underscores the growing interest in inhaled insulin as a non-invasive alternative to traditional injection methods. The potential FDA approval for pediatric use could significantly expand the market for Afrezza, addressing a critical unmet need in diabetes care. The company's focus on real-world dosing and titration patterns highlights its commitment to personalized diabetes management across different patient populations.

Regulatory Approval
Whether the FDA will approve Afrezza for pediatric use by the May 29, 2026 target date.
Market Expansion
How successful MannKind will be in positioning Afrezza as the first needle-free insulin option for pediatric patients.
Clinical Efficacy
The impact of the new data on clinician and patient adoption of Afrezza for both adult and pediatric diabetes management.