Genetic Medicine · Rare Disease

Every patient
deserves a
medicine.

We develop genetic medicines for people living with rare and ultrarare diseases — conditions that have been waiting for the science to catch up. It has. We're building.

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1 in 5k
Boys born with DMD
~70%
DMD patients with one of many rare exons
Our Purpose

Science that knows
who it's for.

This may be the last generation where patients with rare diseases have no real options. In the past two decades, progress has been building up in every component of the complex chain that makes a medicine - effector chemistry, delivery vehicles, target biology, preclinical models, manufacturing solutions, regulatory innovation.

We started Stitch because the time is right. In many cases, we can assemble these tools into a medicine. Antisense chemistry has a clear regulatory path. Muscle delivery has real options. And computational tools can now accelerate the design work that once took years. The patients who have been waiting the longest — children with rare exon deletions in DMD, conditions too small for traditional pipelines — can finally be reached.

We are scientists and engineers. But we are also parents, siblings, and friends. We know the names behind the diagnoses we work on.

Stitching the genetic code
back together.

01 — Platform
Oligonucleotide Medicines

We design antisense oligonucleotides — short, precise sequences that redirect the cellular machinery to skip, silence, or correct broken genetic instructions. Decades of chemistry, refined for the smallest patient populations.

02 — Focus
Rare Exons in DMD

Duchenne Muscular Dystrophy affects many exons — but approved therapies cover only the most common deletions. Children with rare exon deletions have had no options. We are building therapies for exactly those patients, starting now.

03 — Delivery
Getting There

Delivery has always been the bottleneck. We leverage emerging delivery platforms to cut time-to-patient, but we also engineer fit-for-purpose shuttles conjugates on the back of proven mechanisms.

04 — Vision
Ultrarare as a Category

DMD is where we start, not where we stop. Computational design tools now let a small, expert team move across conditions that once required entire discovery organizations. We intend to build medicines for patients who have never had a program designed for them.

Why We're Here
Science moves fast - but for many patients, that's still not fast enough.

The rare disease community has fought hard and won important battles. But for every approved therapy, there are dozens of mutations, thousands of patients, and entire disease subtypes that remain without treatment.

Genetic medicine is uniquely positioned to close this gap — and we intend to use it.

Starting Program · DMD Rare Exons
Duchenne Muscular Dystrophy affects ~1 in 5,000 boys. The majority of affected patients carry deletions amenable to exon skipping — yet only a fraction have an approved therapy. Our first programs target the rare exon deletions that current programs do not include.

How we
work.

We are a small team with deep conviction. We move with urgency because the patients we work for don't have the luxury of time.

🧬
Rigorous

Our science is built on deep mechanistic understanding. We don't cut corners on the biology because we can't afford to be wrong.

🤝
Human

We work closely with patients and families. They are not endpoints. They are the reason every experiment gets done.

Urgent

Children with DMD are losing muscle while timelines slip. We build urgency into every decision, every hire, every experiment.

Let's talk

We're building.
Join us.

Whether you're a scientist, a potential partner, an investor, or a family affected by rare disease — we want to hear from you.