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AC-170 Vehicle

Nicox Ophthalmics, Inc. · Phase 3 active Small molecule Under review

AC-170 Vehicle is a Small molecule drug developed by Nicox Ophthalmics, Inc.. It is currently in Phase 3 development for Ocular hypertension or glaucoma (Phase 3 development).

AC-170 Vehicle is a formulation component designed to deliver the active pharmaceutical ingredient AC-170 to ocular tissues.

AC-170 is a vehicle used in clinical trials for the treatment of allergic conditions such as Allergic Conjunctivitis, Atopic Disease, Rhinitis, and other allergic conditions. It has been tested in concentrations of 0.05%, 0.1%, and 0.24% in studies evaluating its efficacy in treating these conditions.

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 nameAC-170 Vehicle
SponsorNicox Ophthalmics, Inc.
ModalitySmall molecule
Therapeutic areaOphthalmology
PhasePhase 3

Mechanism of action

As a vehicle formulation, AC-170 Vehicle serves as the delivery system for the active drug AC-170, optimizing bioavailability and residence time in the eye. The specific mechanism of AC-170 itself is not publicly detailed, but the vehicle formulation is engineered to enhance ocular penetration and therapeutic efficacy for ophthalmologic conditions.

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 AC-170 Vehicle

What is AC-170 Vehicle?

AC-170 Vehicle is a Small molecule drug developed by Nicox Ophthalmics, Inc., indicated for Ocular hypertension or glaucoma (Phase 3 development).

How does AC-170 Vehicle work?

AC-170 Vehicle is a formulation component designed to deliver the active pharmaceutical ingredient AC-170 to ocular tissues.

What is AC-170 Vehicle used for?

AC-170 Vehicle is indicated for Ocular hypertension or glaucoma (Phase 3 development).

Who makes AC-170 Vehicle?

AC-170 Vehicle is developed by Nicox Ophthalmics, Inc. (see full Nicox Ophthalmics, Inc. pipeline at /company/nicox-ophthalmics-inc).

What development phase is AC-170 Vehicle in?

AC-170 Vehicle is in Phase 3.

Related

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