Next-Generation Ocular Implants

PolyActiva’s pipeline of ocular implants with Prezia™ technology are being developed to offer a safe and effective, fully biodegradable therapy for eye care professionals treating patients with a wide range of ocular diseases.

Latanoprost Acid Ocular Implant - PA5108

Being developed to reduce IOP caused by Open-Angle Glaucoma & Ocular Hypertension
Clinical Investigation Stage: Phase II

Micro implant.
Sustained drug release.

The Target Product Profile for the Latanoprost Acid Ocular Implant, PA5108, currently under development, aims to deliver the following clinical benefits:

PolyActiva achieved study objectives in completed clinical study (NCT03604328) and interim analysis of ongoing study NCT04060758. The Latanoprost Acid Ocular Implant has not been approved by the U.S. Food and Drug Administration (FDA).

IOP Reduction Without Daily Drops

  • Fixed daily dose designed to provide consistent IOP reduction over 6 months
  • Maximum compliance and adherence

Fully Biodegradable

  • No implant persists beyond 4-6 weeks after treatment
  • Additional implants can be safely administered near the end of therapy

Biocompatible

  • Designed to be safe and well tolerated with no immune response, ocular inflammation, or toxicity
  • Zero implant-related ocular adverse events

In-Office Procedure

  • Rapid and minimally invasive administration in outpatient setting
  • Administration integrates into clinical workflow and aligns with patient’s normal visit cycle

Levofloxacin Ocular Implant

Being developed to reduce the risk of Endophthalmitis following ocular (cataract) surgery
Clinical Investigation Stage: Phase I

Micro implant.
Maximum infection
protection.

The Target Product Profile for the Levofloxacin Ocular Implant, currently under development, aims to deliver the following clinical benefits:

Early clinical studies (NCT04682288) conducted by PolyActiva have met clinical trial objectives.
The Levofloxacin Ocular implant has not been approved by the U.S. Food and Drug Administration (FDA)

Reduce Risk of Post-Operative Infection

Fixed daily dose substitutes for peri-operative antibiotics and post-op drop therapy, maximizing compliance and adherence

Fully Biodegradable

No implant remains after 60 days

Biocompatible

Designed to be safe and well tolerated with no immune response, ocular inflammation, or toxicity

Streamlined Procedure

Rapid and minimally invasive administration integrated with cataract surgery