- Affecting about 6 million People, OLP is a persistent inflammatory illness affecting the mucous membranes of the mouth
- No FDA-approved remedy at present exists for OLP
- Affected person registry and OLP examine info is now obtainable
PITTSBURGH, Aug. 22, 2024 (GLOBE NEWSWIRE) — Lipella Prescription drugs, Inc. (NASDAQ: LIPO) has launched an Oral Lichen Planus (OLP) Affected person Registry. This on-line platform is designed to reinforce analysis and drive the event of latest therapies for OLP, a persistent inflammatory illness affecting the mucous membranes of the mouth. Characterised by signs corresponding to burning ache, white patches, swollen tissue, and open sores, OLP impacts roughly 6 million People and at present has no FDA-approved therapies.
The registry is now obtainable, and the location offers extra info on the investigational examine of LP-310 for OLP, an oral rinse derived from the corporate’s lead candidate, LP-10, which is at present being evaluated for hemorrhagic cystitis. LP-310 has obtained FDA approval for medical analysis for the remedy of OLP.
Dr. Michael Chancellor, Chief Medical Officer of Lipella Prescription drugs, acknowledged: We’re happy to introduce this important registry with the goal of accelerating consciousness and accelerating analysis into Oral Lichen Planus, a situation that urgently requires efficient remedy choices for hundreds of thousands of victims throughout the globe.
Dr. Jonathan Kaufman, CEO of Lipella Prescription drugs, added: “We are encouraged by the strong interest from all stakeholders involved in improving patient outcomes and advancing coordinated research for the Oral Lichen Planus community. This registry aligns with our mission to enhance treatment approaches for this challenging condition.
For more information on the LP-310 clinical trial, please visit: https://lipella.com/oral-lichen-planus-treatment/, or visit: https://clinicaltrials.gov/study/NCT06233591.
About Oral Lichen Planus
Oral Lichen Planus is a debilitating condition marked by chronic oral mucosal lesions, which present significant management challenges. The current therapeutic landscape is limited, highlighting the urgent need for innovative solutions. Lipella Pharmaceuticals is addressing this gap through its Phase 2a clinical trial of LP-310, a novel liposomal-tacrolimus oral rinse based on the company’s lead candidate LP-10, which is also being evaluated for hemorrhagic cystitis.
Accessing the Oral Lichen Planus Patient Registry
The Oral Lichen Planus Patient Registry is now available at https://form.jotform.com/242106204151136. Additional information can be found on the American Academy of Oral Medicine’s dedicated page at https://www.aaom.com/oral-lichen-planus.
About Lipella Pharmaceuticals
Lipella is a clinical-stage biotechnology company focused on developing new drugs by reformulating the active agents in existing generic drugs and optimizing these reformulations for new applications. Additionally, Lipella maintains a therapeutic focus on diseases with significant, unaddressed morbidity and mortality where no approved drug therapy currently exists. Lipella completed its initial public offering in December 2022. For more information, please visit www.lipella.com or LinkedIn.
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CONTACT
Dr. Jonathan Kaufman, CEO
Lipella Pharmaceuticals
Info@Lipella.com
1-412-894-1853
Jeff Ramson
PCG Advisory
jramson@pcgadvisory.com
646-863-6893
Supply: Lipella Prescription drugs Inc.
