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Barnetil (SULTOPRIDE)
Barnetil (generic name: SULTOPRIDE) is a sultopride drug. It is currently in Phase 2 development.
Barnetil works by blocking the D(2) dopamine receptor, which helps regulate mood and emotional responses.
Barnetil is a small molecule with the synonyms SULTOPRIDA, SULTOPRIDE, and SULTOPRIDE. It has been studied in clinical trials for various conditions, including Major Depressive Disorder, Post Operative Nausea and Vomiting, Anorexia Nervosa, Clozapine-induced Hypersalivation, and Schizophrenia, with amisulpride being one of the interventions used.
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Baseline phase 2 → approval rate
+15.3pp
Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas). -
CNS / neurology attrition
-3.0pp
CNS drugs have historically high Phase 3 failure rates (notably in Alzheimer disease + major depression).
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2031–2034 | — |
| EMA | EU | 2032–2035 | +0.7 yr |
| MHRA | GB | 2032–2035 | +0.7 yr |
| Health Canada | CA | 2032–2036 | +0.9 yr |
| TGA | AU | 2032–2036 | +1.2 yr |
| PMDA | JP | 2032–2036 | +1.5 yr |
| NMPA | CN | 2033–2037 | +2.3 yr |
| MFDS | KR | 2032–2036 | +1.4 yr |
| CDSCO | IN | 2032–2037 | +1.8 yr |
| ANVISA | BR | 2033–2037 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | SULTOPRIDE |
|---|---|
| Drug class | sultopride |
| Target | D(2) dopamine receptor, D(3) dopamine receptor |
| Modality | Small molecule |
| Therapeutic area | Neuroscience |
| Phase | Phase 2 |
Mechanism of action
Think of dopamine like a messenger in your brain that helps you feel happy and motivated. When Barnetil blocks the D(2) receptor, it can help reduce excessive dopamine activity that may contribute to psychiatric symptoms. This can lead to improved mood and reduced anxiety.
Approved indications
Common side effects
Key clinical trials
- Multicenter Study to Assess the Efficacy and Safety of LB-102 in the Treatment of Adult Patients With BP1MDE. (PHASE2)
- Enhancing Recovery in Early Schizophrenia (PHASE2)
- Characterizing Drug Liking During Drug Administration in Peri-procedural Clinical Settings (EARLY_PHASE1)
- Magnetic Seizure Therapy for Psychotic Disorders (NA)
- Study of Intravenous Amisulpride for Prophylaxis of Post-operative Nausea and Vomiting (PONV) in Pediatric Patients (PHASE2,PHASE3)
- An Investigation of Early Life Stress and Depression (PHASE1)
- Efficacy of Adding Oral Amisulpride to Dual Prophylaxis for Postoperative Nausea and Vomiting in Patients at High Risk for Nausea and Vomiting Undergoing Gynecological Surgery (PHASE2)
- Dopamine Receptor Contributions to Prediction Error and Reversal Learning in Anorexia Nervosa (EARLY_PHASE1)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Barnetil CI brief — competitive landscape report
- Barnetil updates RSS · CI watch RSS
Frequently asked questions about Barnetil
What is Barnetil?
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What is the generic name of Barnetil?
What drug class is Barnetil in?
What development phase is Barnetil in?
What does Barnetil target?
Related
- Drug class: All sultopride drugs
- Target: All drugs targeting D(2) dopamine receptor, D(3) dopamine receptor
- Therapeutic area: All drugs in Neuroscience
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing