# Harrow Inc: Phase 3 study in Postoperative Ocular Inflammation, Postoperative Ocular Pain (250 participants)

**Score:** 65/100

| Field | Value |
|---|---|
| Sponsor | Harrow Inc |
| Sponsor type | Industry (pharma, biotech, medtech) |
| Study | A Phase 3 Study Evaluating the Safety and Efficacy of TRIESENCE® (Injectable Suspension) for the Treatment of Ocular Inflammation and Pain After Ophthalmic Surgery |
| NCT ID | NCT07832552 |
| Phase | Phase 3 |
| Status | enrolling by invitation |
| Conditions | Postoperative Ocular Inflammation; Postoperative Ocular Pain |
| Intervention types | procedure, drug |
| Target enrollment | 250 |
| Site countries | United States |
| Posted | 2026-09-22 |
| Planned start | 2026-05-25 |
| Event | Newly registered study |
| Event date | 2026-09-22 |

## Why this score
- Industry sponsor (buys outsourced services).
- Phase 3: multi-site, larger budget.
- 250 participants planned.

Source: ClinicalTrials.gov (U.S. National Library of Medicine) API v2 (https://clinicaltrials.gov/study/NCT07832552). Last refreshed: 2026-11-04T06:04:38.232Z.
From public ClinicalTrials.gov registrations. Sponsor and study level only: we never list investigators, contacts or participants. A registration describes a planned study and can change. Status changes are read from each study's current status, actual dates and latest posted update, not a full change history, so an update can be a correction rather than a new change. Verify on ClinicalTrials.gov.