Changeflow GovPing Pharma & Drug Safety OCUL101 Neovascular AMD Phase II/III Trial
Routine Notice Added Final

OCUL101 Neovascular AMD Phase II/III Trial

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Summary

ClinicalTrials.gov registered Outlook Therapeutics' Phase II/III trial (NCT07520318) evaluating OCUL101 ophthalmic solution in treatment-naive subjects with neovascular age-related macular degeneration. The study will assess multiple endpoints including change from baseline in best-corrected visual acuity at 12 months.

What changed

Clinical trial NCT07520318 registered for OCUL101, an ophthalmic solution being evaluated for neovascular age-related macular degeneration. The Phase II/III study will enroll treatment-naive subjects to assess efficacy and safety endpoints.

Affected parties including clinical investigators, trial sponsors, and healthcare providers should note the trial is now publicly listed with enrollment eligibility criteria, locations, and study endpoints available for review.

What to do next

  1. Monitor ClinicalTrials.gov for updates to trial status and results

Archived snapshot

Apr 11, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Last updated

Classification

Agency
NLM
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07520318
Docket
NCT07520318

Who this affects

Applies to
Clinical investigators Pharmaceutical companies Healthcare providers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Clinical trial registration Ophthalmic drug research
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Compliance frameworks
GxP
Topics
Pharmaceuticals Medical Devices

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