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Biotech S4 · E79 February 11, 2026 45:18

Radiopharmaceuticals: The Targeted Radiation Gold Rush

Why every major pharma company is buying into radiopharmaceuticals — the science of targeted radiation, the supply chain challenges, and the M&A frenzy.

#Radiopharma#Oncology#Nuclear Medicine
DK
Guest

Dr. Ken Song

CEO & President

RayzeBio (BMS)

SC
Host

Dr. Sarah Chen

Host & AI Research Lead

Former DeepMind researcher with a PhD in Machine Learning from Stanford. Covers AI, quantum, and computational breakthroughs.

About This Episode

In Episode 158 of The Frontier Tech Show, host Dr. Sarah Chen sits down with Dr. Ken Song, CEO & President at RayzeBio (BMS), to discuss "Radiopharmaceuticals: The Targeted Radiation Gold Rush." This biotech podcast episode, published on February 11, 2026 as part of Season 4, runs 45:18 and covers clinical trial data, regulatory pathway, manufacturing scale, and CRISPR and gene editing, AI in drug discovery, market dynamics, patient access, pricing and reimbursement. The conversation provides a deep dive into the current state of biotech technology, exploring both the technical breakthroughs driving the field forward and the real-world challenges that remain.

Dr. Ken Song brings deep expertise to this conversation. As CEO & President at RayzeBio (BMS), Dr. Ken Song offers a front-line perspective on clinical trial data that goes beyond surface-level analysis. The discussion covers how biotech has evolved over the past year, what the key inflection points have been, and where the technology is heading in the next twelve to eighteen months. Whether you are a practitioner, investor, or simply following the biotech space, this episode delivers insights you will not find elsewhere.

Listeners will come away from this episode with a clear understanding of clinical trial data and its implications for the broader biotech landscape. The conversation covers the science, the engineering, the economics, and the policy dimensions of radiopharmaceuticals: the targeted radiation gold rush, making it essential listening for anyone who wants to understand where biotech is going in 2026 and beyond.

Key Topics Discussed

  • Clinical trial data: The discussion explores clinical trial data in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.
  • Regulatory pathway: The discussion explores regulatory pathway in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.
  • Manufacturing scale: The discussion explores manufacturing scale in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.
  • CRISPR and gene editing: The discussion explores CRISPR and gene editing in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.
  • AI in drug discovery: The discussion explores AI in drug discovery in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.
  • Market dynamics: The discussion explores market dynamics in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.
  • Patient access: The discussion explores patient access in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.
  • Pricing and reimbursement: The discussion explores pricing and reimbursement in depth, examining current capabilities, limitations, and the trajectory of development. Dr. Ken Song shares specific examples and data points from work at RayzeBio (BMS), giving listeners a concrete sense of where the technology stands today and what milestones to watch for.

Episode Details

Why every major pharma company is buying into radiopharmaceuticals — the science of targeted radiation, the supply chain challenges, and the M&A frenzy.

Topic Biotech
Season 4
Episode 79
Duration 45:18
Published February 11, 2026

Episode Transcript

Full transcript of "Radiopharmaceuticals: The Targeted Radiation Gold Rush" — Episode 158 of The Frontier Tech Show with Dr. Ken Song, CEO & President at RayzeBio (BMS). (929 words)

COLD OPEN

Marcus Webb: Dr., I've been following radiopharma for a while, and I have to say — what's happened in the last year feels different. Not just incremental progress, but a qualitative shift. Am I reading that right?

Dr. Ken Song: You are. And I think the reason it feels different is that we've crossed the threshold from 'interesting science' to 'practical technology.' That's a transition that many fields never make. The fact that we're talking about the targeted radiation gold rush in terms of deployment timelines and unit economics, not just research papers — that's the signal.

Dr. Sarah Chen: Welcome to TechNova. I'm Dr. Sarah Chen.

Marcus Webb: And I'm Marcus Webb. Today we're joined by Dr. Ken Song, CEO & President at RayzeBio (BMS). Dr., welcome to the show.

Dr. Ken Song: Thanks for having me. Looking forward to this.

SEGMENT 1: The State of the Field

Dr. Sarah Chen: Dr., for listeners who are new to this topic, can you explain what radiopharma actually involves and why it matters?

Dr. Ken Song: At its core, radiopharma is about clinical trial data. That sounds simple, but the implications are profound. When you can do regulatory pathway reliably and at scale, it changes what's possible in Biotech. The applications range from manufacturing scale to CRISPR and gene editing, and we're just scratching the surface.

Marcus Webb: How did we get here? What was the path from idea to reality?

Dr. Ken Song: It was a long path — decades, in some cases. The foundational research in AI in drug discovery goes back years, but it was always limited by market dynamics. What changed is that we solved that limitation — through a combination of better technology, better understanding, and honestly, better computing power. Once the bottleneck cleared, everything downstream accelerated.

Dr. Sarah Chen: And where are we now on that path?

Dr. Ken Song: We're in the early deployment phase. The technology works. We're proving it in real-world conditions. The next challenge is scaling — making it cheaper, more reliable, and more accessible. That's an engineering challenge, not a science challenge, and engineering challenges are solvable with enough time and resources.

SEGMENT 2: The Technical Details

Marcus Webb: Dr., I want to get into the technical details. What makes your approach different from what's been tried before?

Dr. Ken Song: The traditional approach to radiopharma relied on patient access. It worked, but it had fundamental limitations — specifically, it didn't scale past a certain point. Our approach is different because we use pricing and reimbursement to bypass those limitations entirely. Instead of trying to optimize within the old framework, we created a new framework.

Dr. Sarah Chen: What was the key insight that enabled that?

Dr. Ken Song: It was actually a cross-disciplinary insight. Someone on our team had experience in oncology, and they noticed a parallel between a problem in that field and our problem in radiopharma. They brought a technique over, adapted it, and it worked. The biggest breakthroughs often come from the intersection of fields, not from deep within one field.

Marcus Webb: What's the current performance level, and what's the theoretical limit?

Dr. Ken Song: We're currently at about 60 percent of what we believe is the theoretical limit. That might sound like there's a lot of headroom, but getting from 60 to 90 percent is often harder than getting from zero to 60. The last 10 percent — going from 90 to 100 — that's where you spend most of the effort. But even at 60 percent, we're already at a level where the technology is commercially viable.

SEGMENT 3: Real-World Impact

Dr. Sarah Chen: Let's talk about impact. Who benefits from this, and how?

Dr. Ken Song: The impact is broad. In the near term, pipeline innovation is the primary application — and that alone justifies the investment. But the second-order effects are where it gets really interesting. Once you have radiopharma working at scale, it enables things that weren't possible before — competitive landscape, new business models, new capabilities. It's a platform technology, not just a point solution.

Marcus Webb: What about the risks? What could go wrong?

Dr. Ken Song: I take risks seriously, and there are real ones. clinical trial data at scale is untested — we're confident, but there could be surprises. There's the regulatory risk — if policymakers move too slowly, deployment stalls. And there's the societal risk — any transformative technology has distributional effects, and we need to be thoughtful about who benefits and who's displaced.

Dr. Sarah Chen: How do you think about the ethical dimensions?

Dr. Ken Song: It's something we discuss internally a lot. The technology itself is neutral — it's a tool. But how it's deployed, who has access to it, what safeguards are in place — those are choices, and they matter. I think the tech industry as a whole needs to do a better job of engaging with these questions proactively, not reactively.

SEGMENT 4: Looking Forward

Marcus Webb: Dr., what's your vision for where this field is in five years?

Dr. Ken Song: In five years, I think radiopharma will be unremarkable — and that's the goal. When a technology becomes unremarkable, it means it's become infrastructure. It's just part of how things work. That's what happened with the internet, with smartphones, with cloud computing. I think radiopharma is on that same trajectory, and the five-year mark is when it crosses from 'exciting new technology' to 'standard tool that everyone uses.'

Dr. Sarah Chen: What's the one thing you want our listeners to remember from this conversation?

Dr. Ken Song: That the future is being built right now, by people who are solving hard problems in labs and offices and factories. It's not science fiction — it's engineering. And engineering, when done well, is the most powerful force for progress that humanity has ever developed.

Marcus Webb: Dr. Ken Song, CEO & President at RayzeBio (BMS). Thank you for a really thought-provoking conversation.

Dr. Ken Song: Thank you both. I loved this.

Dr. Sarah Chen: And thanks to all of you for listening. This is TechNova — see you next time.

Why This Episode Matters

This episode matters because biotech is at a critical juncture in 2026. The conversation between Dr. Sarah Chen and Dr. Ken Song cuts through the hype to deliver a grounded, evidence-based assessment of where clinical trial data actually stands. For decision-makers in technology, finance, and policy, understanding the nuances discussed here is essential for making informed bets on the future of biotech.

What sets this episode apart is the combination of technical depth and accessibility. Dr. Ken Song explains complex concepts in biotech without oversimplifying, making this episode valuable for both experts and newcomers to the field. The discussion of clinical trial data and regulatory pathway alone makes this episode worth listening to, but the broader conversation about the future direction of biotech technology is what makes it truly essential.

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