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zuojinwan
zuojinwan is a Small molecule drug developed by Nanjing First Hospital, Nanjing Medical University. It is currently in Phase 1 development. Also known as: zuojin pills.
Zuojinwan is being studied in combination with Rabeprazole or Mosapride for the treatment of Functional Dyspepsia combined with Depression in a single-centre randomised controlled study. The conditions being studied also include Functional Dyspepsia, Depression, and Gastroesophageal Reflux Disease, with zuojinwan being compared to Rabeprazole sodium enteric-coated tablets and Mosapride citrate.
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Baseline phase 1 → approval rate
+9.6pp
Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2033–2036 | — |
| EMA | EU | 2034–2037 | +0.7 yr |
| MHRA | GB | 2034–2037 | +0.7 yr |
| Health Canada | CA | 2034–2038 | +0.9 yr |
| TGA | AU | 2034–2038 | +1.2 yr |
| PMDA | JP | 2034–2038 | +1.5 yr |
| NMPA | CN | 2035–2039 | +2.3 yr |
| MFDS | KR | 2034–2038 | +1.4 yr |
| CDSCO | IN | 2034–2039 | +1.8 yr |
| ANVISA | BR | 2035–2039 | +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 | zuojinwan |
|---|---|
| Also known as | zuojin pills |
| Sponsor | Nanjing First Hospital, Nanjing Medical University |
| Modality | Small molecule |
| Therapeutic area | Other |
| Phase | Phase 1 |
Approved indications
Common side effects
Key clinical trials
- Zuojin Wan Combined With Rabeprazole or Mosapride for the Treatment of Functional Dyspepsia Combined With Depression (NA)
- Zuojin Wan Combined With Woonosan Fumarate for the Treatment of GRD Combined With Depression (NA)
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:
- zuojinwan CI brief — competitive landscape report
- zuojinwan updates RSS · CI watch RSS
- Nanjing First Hospital, Nanjing Medical University portfolio CI
Frequently asked questions about zuojinwan
What is zuojinwan?
Who makes zuojinwan?
Is zuojinwan also known as anything else?
What development phase is zuojinwan in?
Related
- Manufacturer: Nanjing First Hospital, Nanjing Medical University — full pipeline
- Therapeutic area: All drugs in Other
- Also known as: zuojin pills
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing