Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**NALSCY** is an investigational fixed-dose sublingual formulation of **buprenorphine + naloxone** developed for opioid dependence. Buprenorphine is a high-affinity partial agonist at the mu-type opioid receptor, reducing opioid withdrawal symptoms and cravings while limiting the pharmacology of full opioid agonists. Naloxone is an opioid-receptor antagonist included primarily to deter parenteral misuse; it has limited bioavailability by the intended sublingual route. Pain Therapeutics licensed European development and commercialization rights to SWYX Pharma while retaining United States rights.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on NALSCY.