USFDA Approves MannKind's Inhaled Insulin Afrezza for Children with Diabetes

Written By :  sheeba farhat
Published On 2026-05-31 05:30 GMT   |   Update On 2026-05-31 05:30 GMT

New Delhi: The U.S. Food and Drug Administration (USFDA) has approved ‌expanded use of MannKind's inhaled rapid-acting insulin in children with diabetes, offering patients under 18 years of age a needle-free treatment option, the company said on ​Friday.

The approval ​broadens treatment options for younger patients who require insulin, often ⁠several times a day, to manage diabetes, a condition where ​the body cannot properly regulate blood sugar levels.

According to Jennifer Segrist, mother ​of 15-year-old Taisie Segrist, who was part of MannKind's research study, her daughter initially needed several injections a day, which was traumatizing for a child her age.

But ​switching to inhaled insulin had been "life changing," making her more independent ​in managing the condition, Segrist told Reuters.

"It really does make a huge difference… ‌diabetes ⁠is not such a huge weight on her shoulders anymore."

Unlike conventional insulin, which is injected subcutaneously and could affect adherence especially in children, MannKind's Afrezza is inhaled through a small device to help control blood ​sugar levels at ​mealtimes.

It was first ⁠approved by the FDA for adults in June 2014.

The drug, approved for use in children aged six ​and above with Type 1 and Type 2 diabetes, ​has ⁠a rapid onset and short duration of action, more closely mimicking the body's natural insulin response to meals. The company said eligible patients can ⁠access ​Afrezza for $35 or less a month.

However, the ​company said Afrezza could cause serious side effects such as sudden lung problems.

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Article Source : Reuters

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