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NCX 470 0.1%

Nicox Ophthalmics, Inc. · Phase 3 active Small molecule

NCX 470 0.1% is a Nitric oxide-donating prostaglandin F analog Small molecule drug developed by Nicox Ophthalmics, Inc.. It is currently in Phase 3 development for Open-angle glaucoma, Ocular hypertension. Also known as: NCX 470.

NCX 470 is a nitric oxide-donating prostaglandin F analog that lowers intraocular pressure by increasing uveoscleral outflow and releasing nitric oxide to enhance trabecular outflow.

NCX 470 is a nitric oxide-donating prostaglandin F analog that lowers intraocular pressure by increasing uveoscleral outflow and releasing nitric oxide to enhance trabecular outflow. Used for Open-angle glaucoma, Ocular hypertension.

Likelihood of approval
58.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% 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 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +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 nameNCX 470 0.1%
Also known asNCX 470
SponsorNicox Ophthalmics, Inc.
Drug classNitric oxide-donating prostaglandin F analog
TargetProstaglandin F receptor (FP receptor); nitric oxide pathway
ModalitySmall molecule
Therapeutic areaOphthalmology
PhasePhase 3

Mechanism of action

NCX 470 combines the intraocular pressure-lowering effects of a prostaglandin F analog with nitric oxide donation. Nitric oxide enhances aqueous humor drainage through both the conventional (trabecular) and unconventional (uveoscleral) pathways. This dual mechanism may provide superior efficacy compared to prostaglandin analogs alone in reducing intraocular pressure in glaucoma patients.

Approved indications

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.

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 NCX 470 0.1%

What is NCX 470 0.1%?

NCX 470 0.1% is a Nitric oxide-donating prostaglandin F analog drug developed by Nicox Ophthalmics, Inc., indicated for Open-angle glaucoma, Ocular hypertension.

How does NCX 470 0.1% work?

NCX 470 is a nitric oxide-donating prostaglandin F analog that lowers intraocular pressure by increasing uveoscleral outflow and releasing nitric oxide to enhance trabecular outflow.

What is NCX 470 0.1% used for?

NCX 470 0.1% is indicated for Open-angle glaucoma, Ocular hypertension.

Who makes NCX 470 0.1%?

NCX 470 0.1% is developed by Nicox Ophthalmics, Inc. (see full Nicox Ophthalmics, Inc. pipeline at /company/nicox-ophthalmics-inc).

Is NCX 470 0.1% also known as anything else?

NCX 470 0.1% is also known as NCX 470.

What drug class is NCX 470 0.1% in?

NCX 470 0.1% belongs to the Nitric oxide-donating prostaglandin F analog class. See all Nitric oxide-donating prostaglandin F analog drugs at /class/nitric-oxide-donating-prostaglandin-f-analog.

What development phase is NCX 470 0.1% in?

NCX 470 0.1% is in Phase 3.

What are the side effects of NCX 470 0.1%?

Common side effects of NCX 470 0.1% include Conjunctival hyperemia, Eye irritation, Increased iris pigmentation, Eyelash growth.

What does NCX 470 0.1% target?

NCX 470 0.1% targets Prostaglandin F receptor (FP receptor); nitric oxide pathway and is a Nitric oxide-donating prostaglandin F analog.

Related

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