Sunnyside, a US-based Alcohol Use Disorder (AUD) treatment and prevention company, announced on Thursday the launch of two new programs that pair semaglutide, a GLP-1 medication, with naltrexone, a medication FDA-approved for alcohol dependence since 1994, as an innovative new option for adults who want to drink less or quit.
Both programs pair medication with Sunnyside's support program, which combines app-based tools and AI-driven personalisation with a layered human support system integrating peer connection, coaches, care coordinators, and licensed clinicians. The company says that insurance is not required.
Sunnyside Med says that its program is designed for prevention and early intervention, with medication prescribed as a first-line treatment, rather than a last resort.
Sunnyside Med's GLP-1 + Naltrexone Microdose Program costs USD199 a month, and the GLP-1 + Naltrexone Full Dose Program costs USD299 a month, plus a one-time USD50 intake fee, with specific BMI requirements for each program. Medication is shipped as an 84-day supply, and members check in with a provider before each refill shipment. Sunnyside Med's naltrexone-only program is still available at USD99 a month. Both new programs are available now, in all 50 states and Washington, D.C.
Semaglutide is not FDA-approved to treat alcohol use disorder.
bioMérieux secures FDA clearance and IVDR CE marking for VITEK PRO diagnostic platform
Compass Pathways completes FDA application for COMP360 in treatment-resistant depression
bioMérieux secures FDA clearance for updated gastrointestinal diagnostic panels
Photocure maintains 2028 Medicare coverage target for AssureMDx following CMS update
Johnson & Johnson reveals new Phase 2 nipocalimab study data in Sjögren's disease
SK Biopharmaceuticals submits cenobamate supplemental New Drug Application to US FDA
Agilent acquires Proscia for USD240m
BeOne Medicines wins FDA Priority Review for BRUKINSA combination in first-line mantle cell lymphoma
United Therapeutics eliminates Pfizer royalty obligations on ralinepag for USD525m
Pentixapharm advances preparationsfor Phase 3 PANDA study
StimLabs launches DermaForm collagen scaffold particulate device
Merck launches Phase 3 trial of Ohtuvayre for COPD exacerbation prevention
Vivesto secures US orphan drug designation for Cantrixil in acute myeloid leukemia