Last reviewed · How we verify
AN2690, 2.5%
AN2690, 2.5% is a sodium-activated potassium channel inhibitor Small molecule drug developed by Pfizer. It is currently in Phase 2 development for Treatment of essential tremor.
AN2690 is a small molecule that acts as a selective and potent inhibitor of the sodium-activated potassium channel, KCNN4.
AN2690 is a treatment being studied for onychomycosis, specifically distal, subungual onychomycosis, and onychomycosis, in clinical trials. The treatment is being tested in different concentrations, including 2.5%, 5%, and 7.5%, in a randomized, double-blind, vehicle-controlled study.
-
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). -
Big-pharma sponsor
+3.0pp
Pfizer is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
| 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 | AN2690, 2.5% |
|---|---|
| Sponsor | Pfizer |
| Drug class | sodium-activated potassium channel inhibitor |
| Target | KCNN4 |
| Modality | Small molecule |
| Therapeutic area | Neurology |
| Phase | Phase 2 |
Mechanism of action
By inhibiting KCNN4, AN2690 is thought to reduce the excitability of neurons and potentially alleviate symptoms of certain neurological disorders. The exact mechanism of action is still being investigated, but it is believed to involve a reduction in the release of neurotransmitters and a decrease in neuronal excitability.
Approved indications
- Treatment of essential tremor
Common side effects
- Headache
- Dizziness
- Nausea
Key clinical trials
- Cumulative Irritation Test (PHASE1)
- Study of Different Doses of a Novel Treatment for Onychomycosis (PHASE2)
- Study of Different Doses of a Novel Treatment for Onychomycosis (PHASE2)
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:
- AN2690, 2.5% CI brief — competitive landscape report
- AN2690, 2.5% updates RSS · CI watch RSS
- Pfizer portfolio CI
Frequently asked questions about AN2690, 2.5%
What is AN2690, 2.5%?
How does AN2690, 2.5% work?
What is AN2690, 2.5% used for?
Who makes AN2690, 2.5%?
What drug class is AN2690, 2.5% in?
What development phase is AN2690, 2.5% in?
What are the side effects of AN2690, 2.5%?
What does AN2690, 2.5% target?
Related
- Drug class: All sodium-activated potassium channel inhibitor drugs
- Target: All drugs targeting KCNN4
- Manufacturer: Pfizer — full pipeline
- Therapeutic area: All drugs in Neurology
- Indication: Drugs for Treatment of essential tremor
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing