Despite addressing a small market, the US Food and Drug Administration approval of ViiV Healthcare’s Cabenuva (cabotegravir, rilpivirine) in adolescents could make a big difference in terms of uptake and adherence of HIV therapy in that age group, the company believes, as well as helping to address some of the lingering stigma around HIV and related psychological issues that adolescent patients face.
ViiV Sees Cabenuva In Adolescents Addressing Adherence, Psychological Distress
Reducing the frequency of dosing to six times a year instead of daily pills could help reduce some of the psychological trauma teens with HIV face, chief medical officer Harmony Garges told Scrip.

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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
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After a long wait for patients, Vykat has become the first drug approved for Prader-Willi syndrome symptoms, opening the market up for Soleno and future challengers.
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