Business of Biotech Shorts
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Ep. 256, Chapter 2: The Investment Landscape Of Psychedelic Drug Development With Srinivas Rao
7/18/2025
Dr. Srinivas Rao discusses the shifting investment landscape for psychedelic therapies. Momentum started to build following the 2019 approval of Spravato®, a form of ketamine used to treat depression. The COVID-19 pandemic brought a surge of biotech investments, fueling rapid growth in the psychedelic space, but that enthusiasm dwindled in late 2021 amid broader biotech downturns. Despite the challenges — regulatory obstacles, market volatility, and a cautious investor pool — promising assets can still attract funding.
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Ep. 256, Chapter 1: Introduction To Srinivas Rao And atai Life Sciences
7/18/2025
Chief Editor of Life Science Leader and Host of The Business of Biotech, Ben Comer, and CEO of atai Life Sciences, Srinivas Rao, M.D., Ph.D., discuss how Rao’s early passion for building and problem-solving led him from electrical engineering to biomedical applications and eventually, to a combined MD/PhD path focused on brain science. In 2018, atai Life Sciences was founded with the intention of delivering psychedelics and other innovative treatments for mental health conditions.
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Ep. 255, Chapter 5: Global Dollars And Sense with Yaniv Sneor
7/11/2025
Sneor clarifies that Mid Atlantic Bio Angels is agnostic to company location, investing across the US and internationally. While European and Asian syndicate partners often seek MAB Angels' investment in their opportunities, they are less inclined to invest in MAB Angels' portfolio companies — a disparity Sneor suggests stems from differences in startup environments, talent, and tolerance for failure across continents. Sneor also discusses his work as CEO of Native State Therapeutics, an early-stage company targeting protein misfolding neurodegenerative diseases like Parkinson's and Alzheimer's. He concludes by commenting upon the shakeup at NIH and FDA, which could influence pharma's R&D focus and ultimately affect MAB Angels' long-term investment strategies.
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Ep. 255, Chapter 4: Executable Exits with Yaniv Sneor
7/11/2025
Sneor points out that that, while Mid Atlantic Bio Angels supports and guides their portfolio companies through liaisons, they do not drive exits; the biotech management teams are expected to possess or acquire that capability. Additionally, Sneor states that opportunities in "buzzy" therapeutic areas like GLP-1s face no less scrutiny. Future market landscape, the biotech’s timeline for acquisition, a robust patent estate and a unique value proposition all must be considered. MAB Angels rarely fills a round alone, but they only refer deals to syndicate partners once they have made an investment decision themselves, which serves as a strong endorsement.
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Ep. 255, Chapter 3: Biotech Investors' Pet Peeves with Yaniv Sneor
7/11/2025
Sneor criticizes "spray and pray" pitches that lack personalization and don't align with the group's specific investment criteria, as well as "scientific pitches" that resemble a poster presentation, rather than a compelling financial story focused on the exit strategy and potential returns. He also cautions that familial relationships can compromise business accountability. Mid Atlantic Bio Angels offers guidance and network access, and they are drawn to opportunities with orphan drug designations that offer potential for expanded indications, or areas so attractive to larger pharma/device companies that early acquisition is likely, providing an efficient path to exit for investors.
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Ep. 255, Chapter 2: Hard Questions Investors Ask with Yaniv Sneor
7/11/2025
Sneor details Mid Atlantic Bio Angels’ considerations when deliberating whether to invest in a biotech startup. The group prioritizes understanding how each biotech plans to monetize its opportunity and achieve a successful exit within five to seven years — looking for a clear path, potential acquirers, and comparable deals — so commercial mindset is as important as scientific prowess. MAB Angels prefers to participate in smaller, syndicated investment rounds of $0.25-$1 million, which allow companies to maintain control and provide consistent progress for investors. Sneor notes that the inherent maturity of biotech companies driven by rigorous data generation and regulatory requirements translates to higher quality investment opportunities.
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Ep. 255, Chapter 1: Yaniv Sneor, Mid Atlantic Bio Angels
7/11/2025
Life Science Leader Chief Editor Ben Comer interviews Yaniv Sneor, co-founder of Mid Atlantic Bio Angels, an angel investor group specializing in life sciences. Sneor and two partners founded the company in 2012 to address the need for specific expertise in diligencing complex life science opportunities. In the past 13 years, the group has attracted an intelligent and engaged membership as well as evolved to an internal fund model. MAB Angels screens more than 100 applications monthly via a diligence process that involves initial gating questions, internal discussions, and a multi-day open voting system with mandatory rationale statements.
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Ep. 254, Chapter 4: LNP Progress & Regulation with Michelle Werner
7/11/2025
Alltrna's lead candidate for genetic diseases utilizes a lipid nanoparticle (LNP) for liver delivery and is currently in IND-enabling studies. LNPs being well-characterized and commercially available allows Alltrna to focus on the novel tRNA payload's safety and efficacy, rather than delivery. Alltrna also is engaging with health authorities to pave the way for its basket trial strategy, which aligns with regulators' stated interest in "many diseases at a time" approaches to address the vast unmet need. Moving forward, Werner says Alltrna's main challenge is transitioning from a research-focused company to one equally weighted in R&D, building clinical capabilities, and securing capital to advance its technology.
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Ep. 254, Chapter 3: What's A Stop Codon Disease? With Michelle Werner
7/11/2025
Welch and Werner discuss Alltrna's patient-first mindset and its practical implications for early-stage rare disease companies. Werner goes on to define the concept of a "stop codon disease" as a reclassification for patients with genetic diseases stemming from a premature termination codon (nonsense mutation). This reclassification, affecting approximately 10% of genetic diagnoses, could allow a single engineered tRNA therapy to address thousands of different life-threatening conditions, offering a universal solution instead of a disease-by-disease approach. Alltrna leverages AI and machine learning to navigate the vast combinatorial space of tRNA designs, optimizing their sequence and chemical modifications for enhanced activity and stability.
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Ep. 254, Chapter 2: Why tRNA? With Michelle Werner
7/11/2025
Alltrna's tRNA technology offers unprecedented ability to universally restore protein function across diverse disease models, regardless of affected gene, protein, or mutation location. For investors, Werner emphasizes the immense unmet need in genetic diseases, explaining how tRNA's universal approach to common nonsense mutations provides a compelling "reason to believe" backed by preclinical and now in vivo data. She highlights the company’s plan to utilize basket trials, a strategy common in oncology, to simultaneously its therapies simultaneously across multiple rare diseases sharing common mutations —not only optimizing development, but also unlocking value in ultra-rare diseases often overlooked due to small individual patient populations.