Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Prometa** is a branded addiction-treatment regimen rather than a single new molecular entity. Public clinical-trial and publication records describe the PROMETA protocol as a **combination of flumazenil, gabapentin, and hydroxyzine**, used off-label with the goal of reducing withdrawal symptoms, craving, and relapse in substance use disorders, particularly methamphetamine dependence. The program was marketed by **Hythiam** and studied in academic trials, including a placebo-controlled UCLA study in methamphetamine abuse, but published controlled evidence found the protocol was **not superior to placebo** for methamphetamine dependence. Because the queried name refers to the branded multi-drug protocol itself, the best annotation is as a **combination pharmaceutical product/program** rather than a distinct single active ingredient.
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 Prometa.