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FP-025 capsules
FP-025 capsules is a Small molecule drug developed by Foresee Pharmaceuticals Co., Ltd.. It is currently in Phase 2 development. Also known as: Adermastat, Placebo.
FP-025 capsules are a small molecule intervention being studied for their effects on allergen-induced airway responses in mild eosinophilic house dust mite-allergic asthma. The capsules are being investigated in clinical trials, including one registered on ClinicalTrials.gov as NCT03858686, where they are being compared to a placebo.
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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).
| 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 | FP-025 capsules |
|---|---|
| Also known as | Adermastat, Placebo |
| Sponsor | Foresee Pharmaceuticals Co., Ltd. |
| Modality | Small molecule |
| Phase | Phase 2 |
Approved indications
Common side effects
Key clinical trials
- The Effect of FP-025, on Allergen-induced Airway Responses in Mild Eosinophilic House Dust Mite (HDM)-Allergic Asthma. (PHASE2)
- Phase 1 Safety, Tolerability and Pharmacokinetics (PK) Study of FP-025 in Healthy Volunteers (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:
- FP-025 capsules CI brief — competitive landscape report
- FP-025 capsules updates RSS · CI watch RSS
- Foresee Pharmaceuticals Co., Ltd. portfolio CI
Frequently asked questions about FP-025 capsules
What is FP-025 capsules?
Who makes FP-025 capsules?
Is FP-025 capsules also known as anything else?
What development phase is FP-025 capsules in?
Related
- Manufacturer: Foresee Pharmaceuticals Co., Ltd. — full pipeline
- Also known as: Adermastat, Placebo
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing