Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Buprenorphine extended-release injection is a long-acting formulation of buprenorphine, a partial mu-opioid receptor agonist and kappa-opioid receptor antagonist, used for the treatment of moderate-to-severe opioid use disorder (OUD). The formulation (specifically the 300 mg/1.5 mL strength) is designed to provide sustained therapeutic plasma levels of buprenorphine over a one-month period following subcutaneous injection. In the context of clinical research led by Pouya Azar, this drug is being evaluated as part of the Symptom-inhibited Naloxone Induction (SINI) protocol. This protocol aims to facilitate a rapid transition for patients from high-potency synthetic opioids (such as fentanyl) to long-acting buprenorphine by using low-dose intravenous naloxone to precipitate mild withdrawal, followed by sublingual buprenorphine/naloxone and a subsequent subcutaneous injection of the extended-release formulation.
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 buprenorphine extended-release injection.