Lipella Pharmaceuticals to Present at PropThink Digital Investor Conference

health news

Chief Medical Officer Dr. Michael Chancellor will discuss hemorrhagic cystitis and the company’s lead candidate, LP-10

PITTSBURGH, Feb. 20, 2024 (GLOBE NEWSWIRE) — Lipella Pharmaceuticals Inc., (Nasdaq: LIPO) (“Lipella,” “our,” “us” or the “Company”), a pioneering, clinical-stage pharmaceutical company, announced today that Chief Medical Officer Dr. Michael Chancellor will present at the PropThink Digital Investor Conference’s key opinion leader (KOL) discussion on Friday, February 23, 2024, at 2 PM ET. Dr. Chancellor’s presentation will be titled: “Urologist Talks Bladder Cancer and Lasting Side Effects”.

PropThink is a leading online destination for investors seeking insights on publicly-traded, emerging growth companies in the healthcare sector.

Webinar Information:
     
Date:   Friday, February 23, 2024
     
Time:   2:00 pm Eastern Time
     
Register Here:   Urologist Talks Bladder Cancer & Lasting Side Effects
     
Presenters:   Dr. Michael Chancellor, CMO, Lipella Pharmaceuticals Inc.
Deniel Mero, Editor PropThink Conferences (Moderator)
     

Topic to include:

  • the urology community’s view on the surge of interest in bladder cancer.
  • the potential of therapies in late-stage development to replace existing, toxic standards of care.
  • why hemorrhagic cystitis (HC) is a large, overlooked opportunity and where existing treatments stand.
  • the promise of using tacrolimus as treatment for HC.
  • Lipella’s expectations for its planned Phase 2b clinical trial evaluating tacrolimus as a treatment for HC.

Following the presentation, investors will have an opportunity to ask relevant questions through an interactive Q&A portal. The webcast link will also be posted on the Investors section of Lipella’s company website, and archived following the event. The above listed dates and times are subject to change.

About LP-10

LP-10 is a liposomal tacrolimus formulation for intravesical administration to treat hemorrhagic cystitis (HC). LP-10 has been evaluated in a multi-center Phase 2a dose escalation trial of 13 subjects with moderate to severe refractory HC. Positive top line results demonstrated safety and efficacy, short duration of systemic uptake of LP-10, and a dose response including decreased hematuria, decreased cystoscopic bleeding and ulceration sites, and improved urinary symptoms in patients. Lipella has been granted Orphan Disease Designation by the FDA for LP-10 in the treatment of moderate to severe hemorrhagic cystitis.

About Hemorrhagic Cystitis

Hemorrhagic cystitis (HC), a severe yet rare condition often triggered by pelvic radiation therapy and specific chemotherapies, is characterized by gross hematuria and currently lacks approved drug treatment. Lipella’s LP-10 stands at the forefront of addressing this unmet medical need.

About Lipella Pharmaceuticals Inc.

Lipella Pharmaceuticals 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.

Forward-Looking Statements
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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