πŸ›οΈ Verified NIH Record β€’ Updated 2025-04-01

Evaluate the Safety of DEXYCU for the Treatment of Inflammation Following Ocular Surgery for Childhood Cataract (NCT05191706)

A Phase 3/4, Prospective, Randomized, Active Treatment-Controlled, Parallel-Design, Multicenter Study to Evaluate the Safety of DEXYCU for the Treatment of Inflammation Following Ocular Surgery for Childhood Cataract

🟒 Recruiting Phase4 πŸ’Š Investigational Drug / Biologic Sponsor: EyePoint Pharmaceuticals, Inc.

🩺 Plain-English Summary (8th-Grade Level)

A Phase 3/4, Prospective, Randomized, Active Treatment-Controlled, Parallel-Design, Multicenter Study to Evaluate the Safety of DEXYCUfor the Treatment of Inflammation Following Ocular Surgery for Childhood Cataract

Who can join: Review the eligibility criteria below.

Location: EyePoint Investigational Site β€” Huntington Beach, California

Age range: Not specified to 3 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (9 Sites)

  • EyePoint Investigational Site β€” Huntington Beach, California
  • EyePoint Investigational Site β€” Palo Alto, California
  • EyePoint Investigative Site β€” Boston, Massachusetts
  • EyePoint Investigational Site β€” Jackson, Mississippi
  • EyePoint Investigational Site β€” Omaha, Nebraska
  • EyePoint Investigational Site β€” Buffalo, New York
  • EyePoint Investigative Site β€” New York, New York
  • EyePoint Investigational Site β€” Rochester, New York
  • EyePoint Investigational Site β€” Charleston, South Carolina

πŸ“ž Contact the Study Coordinator

Phone: (833) 393-7646

Email: rribeiro@eyepointpharma.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Cataract clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—