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% — DRUGPatients 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
- Emma Iacobucci215-662-9393
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Scheie Eye Institute | Philadelphia | Pennsylvania | 19104 | Bennie Jeng, MD |
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