Lipella Pharmaceuticals has completed enrollment in its Phase IIa trial evaluating LP-310, a liposomal tacrolimus oral rinse, for treating oral lichen planus across three dose cohorts at seven US trial sites.
The FDA has approved an Expanded Access Program for LP-310, an innovative oral rinse therapy targeting oral lichen planus, a condition affecting 6 million Americans with no current FDA-approved treatments.
A new report highlights the unmet need for targeted Lichen Planus (LP) treatments, as current options primarily offer palliative care.
Lipella Pharmaceuticals' LP-310, a liposomal-tacrolimus oral rinse, demonstrated statistically significant improvements in treating oral lichen planus (OLP).
Lipella Pharmaceuticals completes the first cohort dosing in its Phase 2a trial of LP-310 for Oral Lichen Planus (OLP).
Lipella Pharmaceuticals received U.S. Patent No. 12,138,345 for its liposomal drug delivery platform, enhancing targeted therapeutic agent delivery.