BRM421 Ophthalmic Solution in Patients With Limbal Stem Cell Deficiency

Part of paid clinical trials in Philadelphia, Pennsylvania.

Sponsor
BRIM Biotechnology Inc.
Study ID
NCT07422389
Status
Available

Conditions

  • Limbal Stem Cell Deficiency (LSCD)

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • BRM421 Ophthalmic Solution, 0.06% — DRUG
    Patients eligible to participate will receive 0.06% BRM421 Ophthalmic Solutions to be administered two times daily (BID, morning and bedtime) on the eligible eye(s). The administration will be at least 12 weeks. The investigator may continue the treatment beyond the 12 weeks based on clinical response. For patients scheduled for LSC transplant, treatment with BRM421 should start only after surgery.

Study Details

The goal of this program is to provide patients with Limbal Stem Cell Deficiency access to the BRM421 eye drops. Participants will: * Use BRM421 two times a day for at least 12 weeks * Visit the clinic monthly for checkups and tests

Key Dates

Status verified
Feb 2026

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Scheie Eye InstitutePhiladelphiaPennsylvania19104
Bennie Jeng, MD

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