| Symbol | HROW |
|---|---|
| Name | HARROW, INC. |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Biotechnology: Pharmaceutical Preparations |
| Address | 1A BURTON HILLS BLVD.,SUITE 200, NASHVILLE, Tennessee, 37215, United States |
| Telephone | +1 615 - 733-4730 |
| Fax | — |
| — | |
| Website | https://www.harrow.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001360214 |
| Description | Harrow Health Inc is an ophthalmology-focused pharmaceutical company. The company is specialized in the development, production, and sale of medications that offer competitive advantages and serve unmet needs in the marketplace. Its cornerstone of ophthalmology program consists of proprietary Dropless Therapy injectable and LessDrops topical formulations that are designed to address patient compliance issues and provide other compelling medical and economic benefits. Additional info from NASDAQ: Additional info from NASDAQ: |
Harrow Acquires Global Rights to TYRVAYA®, the First and Only FDA-Approved Nasal Spray for Dry Eye Disease
Read moreHarrow To Report Second Quarter 2026 Financial Results After Market Close on August 10, 2026
Read moreSamsung Bioepis and Harrow Present Interim Data from a Large-Scale Post-Marketing Surveillance Study on SB11 (BYOOVIZ® / AMELIVU®), a Biosimilar to Lucentis (ranibizumab), at ASRS 2026
Read moreHarrow Highlights Growing Clinical Evidence Supporting IHEEZO® and BYOOVIZ® at ASRS 2026 Annual Meeting
Read moreSamsung Bioepis Relaunches BYOOVIZ® (ranibizumab-nuna) in the United States in Partnership with Harrow
Read moreDirector Sternberg Perry J. 🟢 acquired 5.2K shares (1 derivative) of HARROW, INC. (HROW) Transaction Date: Jun 18, 2026 | Filing ID: 029659
Read moreDirector SILVERNAIL LAUREN P 🟢 acquired 5.2K shares (1 derivative) of HARROW, INC. (HROW) Transaction Date: Jun 18, 2026 | Filing ID: 029658
Read moreDirector Graves Adrienne L 🟢 acquired 5.2K shares (1 derivative) of HARROW, INC. (HROW) Transaction Date: Jun 18, 2026 | Filing ID: 029657
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT07368595 | Comparison of Conjunctival Goblet Cell Density in Dry Eye Patients Treated With… | Phase4 | Dry Eye Disease (DED) | Not_Yet_Recruiting | 2026-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07224529 | Efficacy of Vevye Ophthalmic Solution for the Treatment of Meibomian Gland Dysf… | Phase4 | Meibomian Gland Dysfunction (MGD) | Recruiting | 2026-06-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07566975 | Real-World Assessment of VEVYE® for Short-Term Symptom and Sign Improvement of … | — | Dry Eye | Recruiting | 2026-03-31 | 2026-11-30 | ClinicalTrials.gov |
| NCT07456826 | Study Evaluating the Efficacy and Safety of Chloroprocaine HCl Ophthalmic Gel 3… | Phase4 | Diabetic Macular Edema (DME) | Enrolling_By_Invitation | 2026-03-31 | 2026-08-01 | ClinicalTrials.gov |
| NCT05934253 | The Effects of Low Viscosity Chloroprocaine Ophthalmic Gel 3% on the Bactericid… | Phase4 | Antiseptic | Completed | 2023-07-15 | 2024-02-15 | ClinicalTrials.gov |
| NCT07588074 | Tolerability Comparison of Flarex to Lotemax SM | Phase4 | Ocular Inflammation | Completed | 2021-05-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT02372552 | Microwave Coagulation Using CROMA Electrosurgical System | Na | Polyp of Large Intestine | Completed | 2015-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00157066 | Effects of Vitamin D Supplementation on Antimycobacterial Immunity | Na | Tuberculosis | Completed | 2002-12-01 | 2006-09-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| Vevye(Cyclosporine 0.1% Ophthalmic Solution) | Other | Phase PHASE4 | Meibomian Gland Dysfunction (MGD) | RECRUITING | NCT07224529 |
| Cyclosporine emulsion | Other | Phase PHASE4 | Dry Eye Disease (DED) | NOT_YET_RECRUITING | NCT07368595 |
| Vevye® | Other | Phase PHASE4 | Dry Eye Disease (DED) | NOT_YET_RECRUITING | NCT07368595 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Loteprednol Etabonate Ophthalmic Gel 0.38% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Fluorometholone Acetate Ophthalmic Suspension 0.1% | Other | Phase PHASE4 | Ocular Inflammation | COMPLETED | NCT07588074 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Cyclosporine ophthalmic solution 0.1% | Other | Preclinical | Dry Eye | RECRUITING | NCT07566975 |
| Ergocalciferol | Other | Approved | Tuberculosis | COMPLETED | NCT00157066 |
| Ergocalciferol | Other | Approved | Tuberculosis | COMPLETED | NCT00157066 |
| CROMA | Other | Approved | Polyp of Large Intestine | COMPLETED | NCT02372552 |
| Chloroprocaine ophthalmic gel 3% | Other | Phase PHASE4 | Antiseptic | COMPLETED | NCT05934253 |
| Cyclosporine emulsion | Other | Phase PHASE4 | Dry Eye Disease (DED) | NOT_YET_RECRUITING | NCT07368595 |
| Vevye® | Other | Phase PHASE4 | Dry Eye Disease (DED) | NOT_YET_RECRUITING | NCT07368595 |
| Lidocaine Hydrochloride Injection 2% | Other | Phase PHASE4 | Diabetic Macular Edema (DME) | ENROLLING_BY_INVITATION | NCT07456826 |
| Proparacaine Hydrochloride Ophthalmic Solution 0.5% | Other | Phase PHASE4 | Diabetic Macular Edema (DME) | ENROLLING_BY_INVITATION | NCT07456826 |
| Sham Subconjunctival Injection | Other | Phase PHASE4 | Diabetic Macular Edema (DME) | ENROLLING_BY_INVITATION | NCT07456826 |
| Chloroprocaine Ophthalmic Gel 3% (IHEEZO) | Other | Phase PHASE4 | Diabetic Macular Edema (DME) | ENROLLING_BY_INVITATION | NCT07456826 |
| CROMA | DEVICE | Approved | Polyp of Large Intestine | COMPLETED | NCT02372552 |
| Lidocaine Hydrochloride Injection 2% | DRUG | Phase PHASE4 | Diabetic Macular Edema (DME) | RECRUITING | NCT07456826 |
| Proparacaine Hydrochloride Ophthalmic Solution 0.5% | DRUG | Phase PHASE4 | Diabetic Macular Edema (DME) | RECRUITING | NCT07456826 |
| Sham Subconjunctival Injection | PROCEDURE | Phase PHASE4 | Diabetic Macular Edema (DME) | RECRUITING | NCT07456826 |
| Chloroprocaine Ophthalmic Gel 3% (IHEEZO) | DRUG | Phase PHASE4 | Diabetic Macular Edema (DME) | RECRUITING | NCT07456826 |
| Cyclosporine emulsion | DRUG | Phase PHASE4 | Dry Eye Disease (DED) | NOT_YET_RECRUITING | NCT07368595 |
| Vevye® | DRUG | Phase PHASE4 | Dry Eye Disease (DED) | NOT_YET_RECRUITING | NCT07368595 |
| Vevye(Cyclosporine 0.1% Ophthalmic Solution) | DRUG | Phase PHASE4 | Meibomian Gland Dysfunction (MGD) | NOT_YET_RECRUITING | NCT07224529 |
| Chloroprocaine ophthalmic gel 3% | DRUG | Phase PHASE4 | Antiseptic | COMPLETED | NCT05934253 |