Experts discuss the FDA's priority review of gepotidacin, an oral gonorrhea treatment, highlighting its potential to improve women's health and access to care.
In part 2 of this 7-part Special Report, the panel turned to treatment advances, focusing on the US Food and Drug Administration FDA’s approval of gepotidacin (Blujepa), an oral agent for uncomplicated UTIs in patients aged 12 and older. Moderator Kylee Johnson, MS, ARNP, noted the potential impact for women’s health—particularly among adolescent and adult populations. She emphasized that oral therapies tend to increase acceptance compared with injectable regimens, which often present adherence challenges despite patient awareness of the consequences of untreated infection.
Brooke Redmond, MD, highlighted the relevance for young patients and their families, noting that oral options are typically better received by both adolescents and caregivers. Johnson further underscored how an oral treatment could enhance access in rural and underserved areas, where distance and logistical barriers can delay care. From a public health perspective, she said, faster treatment initiation and easier partner therapy represent major wins in reducing transmission.
Both panelists acknowledged concerns about patient adherence with oral regimens, which require trust that the full course is completed. They agreed that patient counseling will remain central to maximizing efficacy and minimizing resistance. Ultimately, they hope gepotidacin will be a significant innovation that can streamline care, bolster acceptance, and potentially improve treatment rates across diverse patient populations.
Our Experts:
Redmond and Johnson have no relevant disclosures to report. Relevant disclosures for Heaney include Roche.
Get the latest clinical updates, case studies, and expert commentary in obstetric and gynecologic care. Sign up now to stay informed.