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Lantern Pharma Secures EU Patent for AI-Designed Cancer Drug LP-284, Expanding Global Commercialization Efforts

By FisherVista

TL;DR

Lantern Pharma's new patent for LP-284 offers a competitive edge in the $4 billion non-Hodgkin’s lymphoma market, enhancing its global commercialization and partnership potential.

Lantern Pharma's LP-284, developed using AI, targets non-Hodgkin’s lymphoma with a patent securing exclusivity until 2039, streamlining its path through Phase 1 trials.

LP-284's development by Lantern Pharma promises a brighter future for patients with relapsed or refractory non-Hodgkin’s lymphoma, leveraging AI for faster, cost-effective treatments.

Discover how Lantern Pharma's AI-driven LP-284 is revolutionizing cancer treatment, with a new patent paving the way for innovative lymphoma therapies.

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Lantern Pharma Secures EU Patent for AI-Designed Cancer Drug LP-284, Expanding Global Commercialization Efforts

Lantern Pharma (NASDAQ: LTRN) has achieved a significant milestone with the European Patent Office issuing a notice of allowance for a composition of matter patent covering LP-284, its clinical-stage drug candidate aimed at treating relapsed or refractory non-Hodgkin’s lymphoma. This patent, expected to grant exclusivity through 2039, complements existing intellectual property protections in the U.S. and Japan, reinforcing the company's strategy for global commercialization.

LP-284, developed using Lantern Pharma's innovative RADR(R) AI platform, is currently in Phase 1 clinical trials. The drug has already received Orphan Drug Designations for Mantle Cell Lymphoma (MCL) and High-Grade B-Cell Lymphoma (HGBL), highlighting its potential to address unmet medical needs in these areas. Targeting a $4 billion global market, LP-284's development underscores the transformative potential of AI in oncology drug discovery, offering a faster and more cost-effective pathway to bringing life-saving treatments to market.

The significance of this patent extends beyond Lantern Pharma's portfolio. It represents a leap forward in the application of artificial intelligence in drug development, showcasing how AI can reduce the time and cost associated with traditional methods. With an average development timeline of 2-3 years and a cost of approximately $2.5 million per program, Lantern Pharma's approach could set a new standard for the industry, potentially accelerating the availability of innovative cancer therapies.

For patients battling relapsed or refractory non-Hodgkin’s lymphoma, the advancement of LP-284 through clinical trials and towards potential market approval offers hope. The drug's development is a testament to the power of combining cutting-edge technology with medical research, aiming to improve outcomes for those facing this challenging condition. As Lantern Pharma continues to expand its global IP portfolio, the implications for the oncology field and patient care are profound, marking a pivotal moment in the intersection of technology and healthcare.

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FisherVista

FisherVista

@fishervista