Last reviewed · How we verify

FP-025 capsules

Foresee Pharmaceuticals Co., Ltd. · Phase 2 active Small molecule ✓ Verified Jun 2026 Quality 10/100

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.

Likelihood of approval
15.3% vs 15.3% industry baseline
If approved by FDA: likely 2031–2034
Steps remaining: Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • 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).
Predicted approval windows by jurisdiction (conditional on FDA approval)
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 nameFP-025 capsules
Also known asAdermastat, Placebo
SponsorForesee Pharmaceuticals Co., Ltd.
ModalitySmall molecule
PhasePhase 2

Approved indications

Common side effects

No common side effects on file.

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.

SourceUsed for
ClinicalTrials.govTrial 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:

Frequently asked questions about FP-025 capsules

What is FP-025 capsules?

FP-025 capsules is a Small molecule drug developed by Foresee Pharmaceuticals Co., Ltd..

Who makes FP-025 capsules?

FP-025 capsules is developed by Foresee Pharmaceuticals Co., Ltd. (see full Foresee Pharmaceuticals Co., Ltd. pipeline at /company/foresee-pharmaceuticals-co-ltd).

Is FP-025 capsules also known as anything else?

FP-025 capsules is also known as Adermastat, Placebo.

What development phase is FP-025 capsules in?

FP-025 capsules is in Phase 2.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing