Deerfield Beach, FLNCT07675824Now EnrollingIRB Ready

Primary Open Angle Glaucoma (POAG) Clinical Trial in Deerfield Beach, FL

Access cutting-edge primary open angle glaucoma (poag) treatment through this phase 1/2 clinical trial at a research site in Deerfield Beach. Study-provided care at no cost to qualified participants.

Sponsored by Regeneron Pharmaceuticals

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Expert Care in Deerfield Beach

Access primary open angle glaucoma (poag) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related primary open angle glaucoma (poag) treatment provided free

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Check if you qualify for this primary open angle glaucoma (poag) clinical trial in Deerfield Beach, FL

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Why Participate?

  • No-Cost Study Care

  • Local to Deerfield Beach

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Deerfield Beach site if eligible
  4. 4Begin participation

About This Primary Open Angle Glaucoma (POAG) Study in Deerfield Beach

This study will test an experimental drug called REGN22530 ("study drug") to see if it can help treat people with primary open angle glaucoma or ocular hypertension. REGN22530 is an experimental drug that is designed to bind with a protein in the eye that has been shown to cause a buildup of fluid inside the eye and cause increased Intraocular Pressure (IOP). REGN22530 attaches to this protein and stops it from working which may allow more fluid to drain out of the eye and decrease the pressure. The study is looking at: * What side effects REGN22530 might cause * How much REGN22530 is in the blood and eye fluid at different times * If the body has any reactions to REGN22530 (which may cause REGN22530 to not work as well) * How the body and eye pressure respond after having REGN22530, which can help researchers understand why REGN22530 works better in some people than others * How well REGN22530 works

Sponsor: Regeneron Pharmaceuticals

Who Can Participate

Inclusion Criteria

Diagnosis of OHT or POAG of mild to moderate severity as described in the protocol
Best-Corrected Visual Acuity (BCVA) of ≥35 Early Treatment Diabetic Retinopathy Study (ETDRS) letters (Snellen equivalent of better than or equal to 20/200) in the study eye on day 1
BCVA of ≥55 EDTRS letters (Snellen equivalent of better than or equal to 20/80) in the non-study eye on day 1
Phakic or pseudophakic with a posterior chamber intraocular lens that has been implanted ≥3 months prior to Screening Visit 1
Sufficiently clear ocular media, adequate pupillary dilation and fixation to permit quality posterior segment imaging in the study eye Key

Exclusion Criteria

Ocular-specific exclusion criteria apply to the Study Eye only, unless otherwise specified.
OAG or OHT secondary to pigment dispersion, pseudoexfoliation, trauma, uveitis, neovascularization, a vascular disorder, or steroid use
Congenital or traumatic cataract, or visually significant cataract that is likely to require surgical intervention during the study
Presence of significant corneal scarring or irregularities that could interfere with reliable IOP measurement
Prior incisional or bleb-forming glaucoma surgery, suprachoroidal procedures, Trabecular Meshwork (TM)-stripping Microinvasive Glaucoma Surgery (MIGS), angle-based implants other than iStent or iridectomy/iridotomy as described in the protocol
History of Selective Laser Trabeculoplasty (SLT) within 6 months prior to day 1
History of transscleral (including micropulse) or endoscopic cyclophotocoagulation within 1 year prior to day 1 Note: Other protocol defined Inclusion/ Exclusion criteria apply

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Deerfield Beach?

Yes, this clinical trial (NCT07675824) has an active research site in Deerfield Beach, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Primary Open Angle Glaucoma (POAG) Treatment Options in Deerfield Beach, FL

If you're searching for primary open angle glaucoma (poag) treatment options in Deerfield Beach, FL, this clinical trial (NCT07675824) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Deerfield Beach research site is actively enrolling participants for this phase 1/2 clinical trial. You'll receive care from experienced primary open angle glaucoma (poag) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all primary open angle glaucoma (poag) clinical trials near you to find additional studies recruiting in your area.

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