Last reviewed · How we verify
Fumaria
Fumaria, marketed by Shiraz University of Medical Sciences, is positioned in the general toxicity symptom relief segment. The drug's key composition patent is set to expire in 2028, providing a period of exclusivity and potential market protection. The primary risk lies in the lack of detailed clinical trial results and revenue data, which may limit investor confidence and market adoption.
At a glance
| Generic name | Fumaria |
|---|---|
| Sponsor | Shiraz University of Medical Sciences |
| Drug class | Non-Standardized Food Allergenic Extract [EPC] |
| Modality | Small molecule |
| Therapeutic area | Other |
| Phase | FDA-approved |
Approved indications
- General toxicity symptom relief
Common side effects
Key clinical trials
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:
- Fumaria CI brief — competitive landscape report
- Fumaria updates RSS · CI watch RSS
- Shiraz University of Medical Sciences portfolio CI