May 15, 2024 - PSTV
A whisper is building in the oncology world, a whisper carrying the name "rhenium obisbemeda." It's the name of Plus Therapeutics' lead drug candidate, a targeted radiotherapeutic that's showing remarkable results in two devastating forms of brain cancer: Leptomeningeal Metastases (LM) and recurrent Glioblastoma (GBM). While analysts are buzzing about the impressive survival data and the company's aggressive expansion plans, there's a hidden narrative buried within the recent Q1 2024 earnings call transcript [1], a narrative that hints at a seismic shift in the landscape of brain cancer treatment.
Plus Therapeutics, a relatively small biotech with a market cap of roughly $12 million, may be on the cusp of disrupting the current paradigm of radiation therapy, a domain long dominated by big pharma and their expensive, complex external beam radiation therapy (EBRT) machines.
The clue lies in CEO Marc Hedrick's strategic reframe of the GBM development program. He urges us to move beyond seeing rhenium obisbemeda as merely a GBM drug. Instead, he invites us to envision it as the centerpiece of a "novel targeted radiotherapeutic delivery ecosystem," a comprehensive approach that leverages not just the drug's unprecedented radiation dosage, but a suite of cutting-edge technologies: state-of-the-art imaging, custom treatment planning software, neuronavigational technology, and optimized convection-enhanced delivery catheters.
This ecosystem, Hedrick argues, has the potential to not only "improve upon the standard of care in radiation delivery for GBM," but to "leapfrog the primary means of radiation delivery for all CNS neoplasms." This is a bold claim, a claim that goes far beyond the current focus on recurrent GBM and hints at a revolution in the way we approach brain cancer treatment as a whole.
EBRT, the current standard, is limited in the amount of radiation it can deliver. It's also imprecise, often damaging healthy brain tissue. Plus Therapeutics' approach, however, delivers 10x to 20x the radiation dose of EBRT directly to the tumor while minimizing collateral damage.
The data is already showing the promise of this ecosystem. In their Phase 2 GBM trial, Plus Therapeutics reported a median overall survival of 13 months, a staggering 63% improvement over the standard of care. And critically, this was achieved with a single administration of the drug. Imagine the possibilities if multiple doses could be safely delivered.
This is where the hidden narrative takes a dramatic turn. Plus Therapeutics is quietly building a robust supply chain, aiming to have two fully validated GMP manufacturers in place by 2024. This is not merely a move towards commercial readiness for their GBM and LM programs; it's a clear signal that the company is preparing for a much broader application of their technology.
Consider this: The global radiation oncology market is projected to reach $12.5 billion by 2027. If Plus Therapeutics' ecosystem can truly "leapfrog" EBRT as Hedrick suggests, they could capture a significant portion of this market, not just for GBM and LM, but for a wide range of brain cancers.
This ambitious goal is further underscored by their aggressive pursuit of non-dilutive grant funding. They're targeting $10 million in grant applications this year alone, a 43% increase over last year. This influx of capital will fuel their expansion into pediatric brain cancers, further solidifying their position as a leader in targeted radiotherapeutics.
The implications are profound. Plus Therapeutics, with their disruptive ecosystem, could fundamentally alter the treatment landscape for millions of brain cancer patients worldwide. They could render expensive EBRT machines obsolete, providing a more effective, less invasive, and potentially more affordable treatment option. This is not just a win for patients; it's a potential windfall for investors who recognize the magnitude of this impending disruption.
However, there are significant hurdles. Plus Therapeutics will need to replicate their impressive Phase 2 GBM results in larger trials, navigate the complexities of regulatory approval, and overcome the inherent challenges of scaling a complex manufacturing process. Yet, the early data and the company's strategic vision suggest a future where this small biotech, armed with rhenium obisbemeda and its revolutionary ecosystem, could become a dominant force in the fight against brain cancer, leaving Big Pharma scrambling to catch up.
"Hypothesis: Plus Therapeutics' targeted radiotherapeutic delivery ecosystem has the potential to disrupt the radiation oncology market, particularly for CNS neoplasms.Key Numbers:Global radiation oncology market projected to reach $12.5 billion by 2027.Plus Therapeutics' Phase 2 GBM trial showed a 63% improvement in median overall survival compared to standard of care. The company is building a robust supply chain, capable of producing commercial-scale quantities of rhenium obisbemeda. Plus Therapeutics is targeting $10 million in non-dilutive grant funding in 2024."
To illustrate Plus Therapeutics' commitment to its goals, let's analyze its recent financial performance based on its Q1 2024 and Q4 2023 earnings calls [1, 2]:
As a development-stage biotech company, Plus Therapeutics is not yet profitable. However, the significant grant revenue and recent private placement financing of up to $19.25 million [1] demonstrate strong support for its development programs. The company is strategically managing its resources to advance its clinical trials and build a commercially viable supply chain.
Reference: [1]
"Fun Fact:Rhenium-186, the radioisotope used in rhenium obisbemeda, is a relatively new medical isotope. Its unique properties make it ideal for targeted radiation therapy, allowing for precise delivery of high radiation doses to tumors while minimizing damage to surrounding healthy tissue."