COMPOUND WITH CONFIDENCE: PCCA Membership, $895/month.
Stay current on PCCA news and events, market trends, and all things compounding!
In the world of GLP-1 receptor agonists, semaglutide has become a key player for several health conditions. But with growing patient demand and evolving regulations, healthcare providers are looking beyond traditional injections to explore new ways to deliver this powerful therapy.
One of the most promising alternatives? Sublingual administration.
In this article, we’ll discuss several considerations for sublingual semaglutide, including patient care and regulatory compliance.
Peptide drugs like semaglutide are notoriously difficult to deliver orally; when taken by mouth, up to 1% of the drug is absorbed under ideal conditions.
Sublingual dosing offers an alternative route of administration by allowing absorption directly into the bloodstream through the mucosal tissue, bypassing the gastrointestinal system and first-pass metabolism. This may improve bioavailability and make therapy more accessible for patients who struggle with injections.
Sublingual therapy isn’t as simple as “place and swallow.” For improved absorption, the medication should stay in contact with the sublingual or buccal tissue for as long as possible.
The minimum hold time is 30 seconds, but ideally, patients should aim for 5 to 15 minutes. Increased contact time with the sublingual tissue may help with sublingual absorption. Swallowing the compounded preparation would likely result in very limited absorption.
Sublingual semaglutide should follow a titration approach, with typical starting doses of 0.75 mg to 1 mg daily for new patients. Increase the dose every 4 weeks, if needed, based on patient response.
While GLP-1 medications like semaglutide are best known for their role in weight management and diabetes, emerging research is pointing to broader therapeutic potential, including:
As with any GLP-1 therapy, thoughtful patient selection and regular monitoring are essential, with special attention paid to:
Compounded semaglutide, whether sublingual or injectable, sits under a shifting regulatory microscope. Shortages of commercial GLP-1 drugs initially opened the door for compounding, but as supply chains recover, the rules are tightening.
Key points for pharmacies:
An important takeaway from the latest research and clinical experience is that patient care must remain personalized. Flexibility and close monitoring are essential.
Sublingual semaglutide is more than just an alternative to injections — it represents a significant opportunity to improve access, adherence and possibly unlock new therapeutic applications.
As with any evolving treatment landscape, the best results come from careful dosing, ongoing education and staying current on regulatory developments.
Whether you’re a prescriber, pharmacist or patient, the message is clear: Personalized care, open communication and compliance are the keys to success.
PCCA members with clinical services access may contact our Clinical Services team for help with sublingual semaglutide and other compounding concerns.