The approval extends the use of Liletta for an additional two years. It is the only hormonal IUD approved for continuous use up to eight years.
The FDA has approved Medicines360’s supplemental new drug application (sNDA) to extend the duration of use of Liletta (levonorgestrel-releasing intrauterine system). It is now extended to prevent pregnancy for up to eight years; previously the device could be used for up to six years. With this FDA approval, Liletta one of the longest approved durations of use for a hormonal intrauterine device (IUD) in the United States. The IUD first received approval in 2015.
Tina Raine-Bennett, M.D.
“As a nonprofit, mission-driven pharmaceutical organization, we are committed to closing critical gaps in women’s healthcare and ensuring that women have access to the medicines and devices they need to live their best and fullest lives,” Tina Raine-Bennett, M.D., chief executive officer of Medicines360, said in a press release.
This approval is based on data from ACCESS IUS study that Medicines360 first published in the American Journal of Obstetrics and Gynecology in May 2022. The phase 3 clinical trial recruited 1,751 women in the United States. Liletta was about 99% effective in preventing pregnancy for up to eight years in a diverse population of women. No new safety concerns arose with extended use. Among the most common reported events were Vulvovaginal infections with bacteria or yeast and urinary tract infections.
The wholesale acquisition of Liletta is $845.10, according to AbbVie. Medicines360 and AbbVie have partnered for the marketing of Liletta.
Trelegy and Breo Offer Incremental Improvement Over Generics
March 3rd 2025The Institute for Clinical and Economic Review has prepared a special report on Trelegy and Breo, two therapies that treat patients with chronic obstructive pulmonary disease that are part of CMS's drug price negotiation program.
Read More
In this episode of the "Meet the Board" podcast series, Briana Contreras, Managed Healthcare Executive editor, speaks with Ateev Mehrotra, a member of the MHE editorial advisory board and a professor of healthcare policy and medicine at Harvard Medical School. Mehtrotra is also a hospitalist at the Beth Israel Deaconess Medical Center in Boston. In the discussion, Contreras gets to know Mehrotra more on a personal level and picks his brain on some of his research interests including telehealth, alternative payment models and price transparency.
Listen
FDA Accepts sNDA for Zoryve Cream for Atopic Dermatitis Treatment in Young Children
February 26th 2025This once-daily topical treatment is the latest phosphodiesterase-4 (PDE4) inhibitor designed for mild to moderate atopic dermatitis (AD) in children aged 2 to 5 years. The PDUFA target action date of October 13, 2025, is set for its decision on the application.
Read More
FDA Accepts BLA Resubmission for Follicular Lymphoma Drug, Odronextamab
February 26th 2025The FDA has accepted the biologics licensing application (BLA) resubmission for odronextamab, a potential treatment for relapsed/refractory follicular lymphoma and diffuse large B-cell lymphoma.
Read More