The tools of drug creation are compounding. We back the platforms where they meet.

We’re a science-native venture firm.

We underwrite the biology first, then back the builders of what drug creation is becoming.

Why now

Drug creation is maturing faster than ever.

For the first time, the three tools of drug creation are advancing at once: we can start from causally-validated human biology, design a molecule to spec instead of screening and hoping, and deliver it to tissues that were out of reach a few years ago.

Together, these shifts raise the probability that a drug works.

The full thesis →
01 · The target

Start from causally-validated biology

Human genetics now lets a company begin from a causally-validated target. Genetically-supported targets look roughly twice as likely to reach approval, which goes after the biggest reason drugs fail.

Sources: Nelson et al., Nature Genetics (2015); King, Davis & Degner, PLoS Genetics (2019).

02 · The molecule

From screen-and-hope to design-to-spec

Design is starting to replace search. Since AlphaFold, de novo protein and sequence models let founders specify the binder or enzyme they need and, increasingly, get it.

03 · The delivery

Delivery is opening, tissue by tissue

For a decade the constraint was rarely the payload; it was reaching the right tissue. The advances that opened the liver are now reaching muscle, the CNS and immune cells.

If your edge is the science

We invest in the science before it’s obvious.

Building a biotech company, or considering liquidity in one?