The $2 Million Problem: Why Life-Saving Cell Therapies Can't Get Paid

A cell therapy turns a 2-month death sentence into 5 years of life. The company that made it is struggling to survive. Here's why — and what might fix it.

Jennifer Hinkel, MSc CHW FRSA consults on pharmaceutical market access and health policy through Sigla Sciences. Previously at Roche/Genentech and co-founder of a market access consultancy focused on health economics for high-cost oncology drugs. She holds patents on data containerization and tokenization methods for outcomes-based contracting.

Based on an interview with Jennifer Hinkel · Edited by Dr. Dominik Dotzauer

The Disconnect

Jennifer Hinkel has seen the future of medicine. It's spectacular. And it's broke.

Hinkel spent years at Roche and Genentech on the market access side. She co-founded a consultancy focused on health economics for high-cost oncology drugs. She's been in biopharma long enough to know when something is fundamentally broken.

"One of my consulting clients is a cell therapy company, and they're struggling. Their stock price is tanked. They have a drug that is really phenomenal — a game-changing drug in cancer."

The numbers are staggering: Patients who had exhausted all options — two months to live — are now alive five years later. Twenty percent of responders. From terminal to thriving.

2 mo → 5 yrs
Life expectancy for 20% of responders
"That is major value there. But the product innovator gets paid once, and they don't get any extra."

Once. For five years of life.

The company isn't struggling because the science failed. The science is miraculous. They're struggling because the business model is broken.

"We don't need to bring the price down. We need to shift the risk. It's a risk pricing problem, not a drug pricing problem."

The 12-Month Trap

Here's how healthcare payment works in the US:

Payers budget in 12-month cycles. They're looking at this year's expenses, this year's premiums, this year's bottom line.

"The payer is set up to price risk over a 12-month period. They're not set up to price risk or to hold risk over long times."

A $2 million cell therapy hits that budget like a meteor. Even if the patient lives another decade, even if they go back to work, pay taxes, raise kids — none of that shows up on the insurer's spreadsheet.

Worse: Hereditary diseases run in families. What if a family transfers into your health plan and two kids need gene therapy? That's a catastrophic financial event for your 12-month budget.

The misalignment: Pharma wants payment when the drug goes in the patient. Payers can only manage 12-month risk windows. Neither is set up to capture long-term value. So life-saving therapies sit on shelves while companies burn cash.

Wall Street Is Hungry

Here's what's interesting: Finance wants this problem.

"Talking to people in the finance industry, they would be hungry for that risk because it's an uncorrelated risk to equities markets. Clinical performance of a drug in a patient population is not correlated with how the stock market's performing."

Hedge funds, pension funds, banks — they're always looking for new instruments. Risks that don't move with the S&P 500. Healthcare outcomes are exactly that kind of risk.

But here's the problem:

"Finance people and biotech people don't talk to each other and don't understand each other. It's a completely different paradigm."

Hinkel has been working on this for nine years. Since 2017. She's patented data containerization and tokenization methods for outcomes-based contracting. The infrastructure exists. The translation layer doesn't.

The Pension Fund Paradox

Want to understand how weird healthcare finance gets? Consider pension funds.

"Pension funds are terrified that we're going to get an Alzheimer's blockbuster."

Think about it: Pension funds stop paying when beneficiaries die. A cure for a leading cause of death? That's bad for their balance sheet.

"COVID has been great for them because COVID took down overall life expectancy. So they're looking for hedges in the biotech sector where they could get some upside if one of these paradigm-shift drugs happens."

The money is there. The appetite is there. What's missing is a way for these capital holders to buy into healthcare outcome risk.

How It Could Work

Hinkel describes a model with three parties: Pharma, Payer, and a new Third-Party Finance layer.

For Pharma: Instead of hoping for $2 million (which they won't get after contracting anyway), they get $1 million upfront plus residuals tied to patient milestones. Maybe a kicker at every five-year survival milestone.

For Payers: Instead of a $2 million budget bomb, they pay a monthly subscription into a fund — like reinsurance for catastrophic events. Families move in and out of plans; the risk gets spread across the whole pool.

"It should feel like a reinsurance model to the payer. For pharma, it should feel like they're getting upfront net present value with potential long-tail rewards."

For Finance: They hold the long-term risk. They might even invest in early-stage biotechs and negotiate better pricing as part of the deal. The ecosystem creates new incentives.

The Weather Derivatives Guy

This isn't just theory. People are building adjacent infrastructure.

Hinkel describes a collaborator whose team came from parametric insurance and weather derivatives:

"You can buy risks, such as: I want a payout if the measured wind speed hits 150 miles an hour at the Miami airport. It's a hurricane hedge. Very specific, time-bound."

His team is now applying the same model to healthcare costs — building indices and instruments around hospital collections, insurance payouts, cost benchmarks.

Companies are beginning to build tradeable indices around healthcare costs — think S&P 500 for medical expenses — partnering with insurers so health systems can hedge against unexpected costs.

The infrastructure for healthcare derivatives is emerging. The question is whether pharma, payers, and regulators can align.

The 2008 Question

You're thinking it: "Didn't securitization cause a global financial crisis?"

Yes. And Hinkel is thinking about it too.

"The risk here — what we want to protect against — is things that could be like: 'I'm exposed if somebody has a disease that needs a gene therapy, so I'm going to send a hitman out to kill babies with that genetic disease.' I know that sounds crazy, but that's the kind of perverse incentive we need to design against."

Less extreme but equally important: preventing funds from profiting when therapies fail, or having incentives to deny treatment.

Proposed safeguards:

The mortgage crisis happened partly because no one understood what was in the bundles. Healthcare securitization would need radical transparency.

What This Means for Biotech BD

If you're in business development at a cell therapy company, you're living this problem daily.

You have a product that works. Clinical data that's undeniable. And a market that can't figure out how to pay for it.

The financing conversation used to be "What's your price?" Now it's "What's your payment model?" Outcomes-based contracts. Risk-sharing agreements. Creative structures that didn't exist five years ago.

This is where biotech BD is heading. Not just selling drugs — architecting deals.

The companies that figure out how to work with third-party finance, how to structure outcome-contingent payments, how to spread risk across larger pools — those are the ones that will survive the CGT reimbursement crisis.


Jennifer Hinkel, MSc CHW FRSA, consults on pharmaceutical market access and health policy through Sigla Sciences. Previously at Roche/Genentech and co-founder of a market access consultancy focused on health economics for high-cost oncology drugs. She holds patents on data containerization and tokenization methods for outcomes-based contracting.

Get smarter about biotech in 5 minutes

Join 2,700+ biotech & pharma professionals. Daily M&A, trials, FDA decisions.