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Lantern Pharma Achieves Milestone in Phase 2 HARMONIC Trial for Non-Smoker NSCLC Patients

By FisherVista

TL;DR

Lantern Pharma's early completion of Phase 2 HARMONIC trial enrollment in Japan positions it ahead in targeting never-smoker NSCLC markets with its AI-driven LP-300 therapy.

Lantern Pharma's Phase 2 HARMONIC trial uses the RADR platform to assess LP-300 combined with carboplatin and pemetrexed in never-smoker NSCLC patients post tyrosine kinase inhibitors.

Lantern Pharma's AI-driven cancer therapies aim to improve survival rates and quality of life for never-smoker NSCLC patients globally, starting with Japan and Taiwan.

Lantern Pharma leverages AI to fast-track cancer drug development, showing an 86% clinical benefit rate in early U.S. trials for never-smoker NSCLC.

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Lantern Pharma Achieves Milestone in Phase 2 HARMONIC Trial for Non-Smoker NSCLC Patients

Lantern Pharma (NASDAQ: LTRN), a pioneer in AI-driven oncology drug development, has successfully completed the targeted enrollment for its Phase 2 HARMONIC clinical trial in Japan ahead of schedule. This trial, focusing on never-smoker non-small cell lung cancer (NSCLC) patients who have progressed after tyrosine kinase inhibitors, represents a critical advancement in the fight against a subtype of lung cancer that disproportionately affects certain populations.

The trial, which has enrolled 10 patients across five sites including the National Cancer Center Japan, evaluates the efficacy of LP-300 in combination with carboplatin and pemetrexed. This milestone not only underscores Lantern Pharma's commitment to addressing unmet medical needs but also validates its international expansion strategy into regions with a higher prevalence of never-smoker NSCLC, such as Japan and Taiwan.

According to CEO Panna Sharma, the early completion of enrollment in Japan is a testament to the potential of LP-300, building on early U.S. data that showed an 86% clinical benefit rate, including a durable complete response lasting nearly two years. The global trial aims to enroll approximately 90 patients, further exploring the therapeutic benefits of LP-300 in a broader patient population.

The significance of this development cannot be overstated. NSCLC accounts for the majority of lung cancer cases worldwide, and never-smoker NSCLC presents unique challenges in treatment. Lantern Pharma's innovative approach, leveraging its proprietary RADR(R) platform, which utilizes over 100 billion oncology-focused data points, could revolutionize the way we treat this devastating disease. For more information on Lantern Pharma's groundbreaking work, visit https://ibn.fm/IcDma.

This trial's progress is a beacon of hope for patients and a significant milestone for the oncology community, demonstrating the power of AI in accelerating drug development and bringing life-changing therapies to those in need. With an estimated combined annual market potential of over $15 billion USD for its pipeline, Lantern Pharma is at the forefront of transforming cancer treatment.

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FisherVista

FisherVista

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