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Lipella Pharmaceuticals Unveils Advanced Bladder Imaging Technique at ICICJ Conference

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Lipella Pharmaceuticals (Nasdaq: LIPO) is set to present clinical data on LP-20, a novel MRI contrast agent, at the 5th International Consultation on Interstitial Cystitis Japan (ICICJ) in Kyoto, August 21-23, 2024. LP-20 is designed to diagnose interstitial cystitis and detect bladder cancer using advanced MRI technology to identify bladder permeability defects.

The contrast agent, which has completed preclinical and proof-of-concept human trials, is administered via catheter into the bladder. It shows promise as a rapid and cost-effective diagnostic solution for these conditions. LP-20's development was partially funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

Lipella Pharmaceuticals (Nasdaq: LIPO) presenterà dati clinici su LP-20, un nuovo agente di contrasto per risonanza magnetica, durante la 5ª Consultazione Internazionale sull'Interstiziale Cistite in Giappone (ICICJ) a Kyoto, dal 21 al 23 agosto 2024. LP-20 è progettato per diagnosticare cistite interstiziale e rilevare cancro alla vescica utilizzando una tecnologia avanzata per la risonanza magnetica in grado di identificare difetti nella permeabilità della vescica.

L’agente di contrasto, che ha completato studi preclinici e prove di fattibilità su soggetti umani, viene somministrato tramite catetere direttamente nella vescica. Mostra promettenti potenzialità come soluzione diagnostica rapida ed economica per queste condizioni. Lo sviluppo di LP-20 è stato parzialmente finanziato dal National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

Lipella Pharmaceuticals (Nasdaq: LIPO) presentará datos clínicos sobre LP-20, un nuevo agente de contraste para resonancia magnética, en la 5ª Consulta Internacional sobre Cistitis Intersticial Japón (ICICJ) en Kioto, del 21 al 23 de agosto de 2024. LP-20 está diseñado para diagnosticar cistitis intersticial y detectar cáncer de vejiga utilizando tecnología avanzada de resonancia magnética para identificar defectos en la permeabilidad de la vejiga.

El agente de contraste, que ha completado ensayos preclínicos y pruebas de concepto en humanos, se administra a través de un catéter en la vejiga. Muestra un gran potencial como una solución diagnóstica rápida y rentable para estas condiciones. El desarrollo de LP-20 fue parcialmente financiado por el National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

립엘라 제약 (Nasdaq: LIPO)는 2024년 8월 21일부터 23일까지 일본 교토에서 열리는 제5회 국제 간질성 방광염 상담에서 LP-20에 대한 임상 데이터를 발표할 예정이다. LP-20은 방광의 투과성 결함을 식별하기 위해 고급 MRI 기술을 사용하여 간질성 방광염 진단과 방광암 감지를 위해 설계되었다.

이 조영제는 preclinical 및 개념 증명 임상 시험을 완료하였으며, 방광에 카테터를 통해 투여된다. 이러한 질환에 대한 빠르고 비용 효율적인 진단 솔루션으로서의 가능성을 보여준다. LP-20의 개발은 국립 당뇨병 및 소화기 및 신장 질환 연구소(NIDDK)의 일부 자금 지원을 받았다.

Lipella Pharmaceuticals (Nasdaq: LIPO) est sur le point de présenter des données cliniques sur LP-20, un nouvel agent de contraste pour l'IRM, lors de la 5e Consultation Internationale sur la Cystite Interstitielle au Japon (ICICJ) à Kyoto, du 21 au 23 août 2024. LP-20 est conçu pour diagnostiquer la cystite interstitielle et détecter le cancer de la vessie en utilisant une technologie IRM avancée pour identifier les défauts de perméabilité de la vessie.

L'agent de contraste, qui a terminé des études précliniques et des essais de preuve de concept sur des humains, est administré par cathéter dans la vessie. Il montre un potentiel prometteur en tant que solution de diagnostic rapide et économique pour ces conditions. Le développement de LP-20 a été en partie financé par le National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

Lipella Pharmaceuticals (Nasdaq: LIPO) wird klinische Daten zu LP-20, einem neuartigen Kontrastmittel für die Magnetresonanztomographie, auf der 5. Internationalen Konsultation zur Interstitiellen Zystitis in Japan (ICICJ) in Kyoto vom 21. bis 23. August 2024 präsentieren. LP-20 ist darauf ausgelegt, interstitielle Zystitis zu diagnostizieren und Blasenkrebs mithilfe fortschrittlicher MRI-Technologie zu erkennen, um Permeabilitätsdefekte der Blase zu identifizieren.

Das Kontrastmittel, das präklinische und Machbarkeitsstudien am Menschen abgeschlossen hat, wird über einen Katheter in die Blase eingebracht. Es zeigt vielversprechende Ansätze als schnelle und kostengünstige diagnostische Lösung für diese Erkrankungen. Die Entwicklung von LP-20 wurde teilweise vom National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) finanziert.

Positive
  • Completion of preclinical and proof-of-concept human trials for LP-20
  • Potential for LP-20 to be a rapid and cost-effective diagnostic solution
  • Partial funding from NIDDK for LP-20 development
Negative
  • None.

  • LP-20 contrast agent designed to diagnose interstitial cystitis and detect bladder cancer
  • Novel MRI contrast agent, which received support from National Institute of Diabetes and Digestive and Kidney Diseases
  • 5th International Consultation on Interstitial Cystitis Japan runs Aug. 21-23 in Kyoto

PITTSBURGH, Aug. 21, 2024 (GLOBE NEWSWIRE) -- Lipella Pharmaceuticals Inc. (Nasdaq: LIPO), a clinical-stage biotech company, will highlight clinical data on LP-20, a novel MRI contrast agent designed for diagnosing interstitial cystitis and detecting bladder cancer at the 5th International Consultation on Interstitial Cystitis Japan (ICICJ) in Kyoto, Japan, taking place August 21-23, 2024.

LP-20, which has completed preclinical and proof-of-concept human trials, is administered via catheter into the bladder. It uses advanced MRI technology to identify bladder permeability defects, aiding in the diagnosis of interstitial cystitis and bladder pain syndrome (IC/BPS) and the detection of bladder cancer progression to muscle invasive bladder cancer. Funded, in part by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), LP-20 shows promise as a rapid and cost-effective diagnostic solution for these conditions.

Dr. Michael Chancellor, Chief Medical Officer at Lipella, commented, “The use of MRI to measure bladder permeability defects offers a potential breakthrough in diagnosing IC/BPS and bladder cancer. This innovative imaging technique addresses significant unmet needs in urology and could greatly enhance patient care. We look forward to sharing our findings with the international scientific community as we continue to develop needed therapeutics for serious diseases.”

Professor Pradeep Tyagi from the University of Pittsburgh Medical Center added, “LP-20 provides a valuable tool for phenotyping IC/BPS, potentially streamlining patient identification for clinical trials and improving timely access to effective treatments.”

Convening international leaders in the field of interstitial cystitis, the 5th International Consultation on Interstitial Cystitis Japan will feature special lectures and workshops on pelvic pathology, and the proceedings will be published in a special issue of “The International Journal of Urology,” the official English journal of the Japanese Urological Association.

About LP-20

LP-20 is a dual-component MRI contrast agent designed to identify bladder permeability defects. Administered via catheter, it generates detailed MRI images to diagnose IC/BPS and monitor bladder cancer progression. It represents a significant advancement in bladder diagnostics, offering a non-invasive alternative to traditional methods.

About Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) and Bladder Cancer

IC/BPS is a challenging condition often diagnosed by exclusion. Current diagnostic methods, including cystoscopy, are limited in differentiating IC/BPS from pelvic floor dysfunction. A new diagnostic tool for bladder permeability could expedite diagnosis and reduce patient suffering. Bladder cancer diagnosis, particularly for muscle invasive bladder cancer, traditionally relies on invasive procedures like cystoscopy and biopsy. LP-20 aims to complement existing methods with a non-invasive, early-detection imaging technique.

ABOUT LIPELLA PHARMACEUTICALS INC.

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, trading on Nasdaq under the ticker LIPO. For more information, please visit www.lipella.com or LinkedIn.

Forward-Looking Statements

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CONTACT
Jonathan Kaufman
Lipella Pharmaceuticals
Info@Lipella.com
1-412-894-1853

Jeff Ramson
PCG Advisory
jramson@pcgadvisory.com
646.863.6341


FAQ

What is LP-20 and what is it designed for?

LP-20 is a novel MRI contrast agent developed by Lipella Pharmaceuticals (LIPO) designed to diagnose interstitial cystitis and detect bladder cancer. It uses advanced MRI technology to identify bladder permeability defects.

When and where is Lipella Pharmaceuticals presenting data on LP-20?

Lipella Pharmaceuticals is presenting clinical data on LP-20 at the 5th International Consultation on Interstitial Cystitis Japan (ICICJ) in Kyoto, taking place August 21-23, 2024.

What stage of development is LP-20 currently in?

LP-20 has completed preclinical and proof-of-concept human trials, showing promise as a diagnostic tool for interstitial cystitis and bladder cancer.

How is LP-20 administered to patients?

LP-20 is administered via catheter directly into the bladder of patients.

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