SNAPSNAPBiosciences

One cell.One adaptor.Multiple targets.

We are developing a novel switchable CAR-T/NK cell platform for the treatment of cancer and autoimmune disorders.

01 — About us

The future of cell therapy is Programmable.

We are SNAP Bio, a wholly-owned subsidiary of Coeptis Holdings, Inc.

Our switchable CAR-T/NK platform is designed to overcome major limitations of conventional “hard-wired” CAR designs, as well as outperform the new class of “switchable” CAR prototypes.

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02 — Our Science

One adaptor. Multiple antigens.

Switching the adaptor to switch the target isn’t new. What is: a single adaptor that engages two or more antigens at once. One cell, one adaptor, multiple targets.

Conventional CAR

Hard-wired to one target

The receptor is fixed to a single antigen — maybe two. Every new target means re-engineering the whole cell.

Other switchable CARs

Swappable, still single-target

Change the adaptor to change the target — but each adaptor still binds just one antigen at a time.

SNAP-CAR

Switchable and multi-antigen

A single adaptor engages two or more antigens at once. Switch the adaptor, switch the target — and hit several together.

03 — Our chemistry

Why “SNAP” is better.

A switchable CAR grips its adaptor with affinity on both sides — a bond that is always half-letting-go. Receptor signaling stutters, so the target has to be densely expressed for the cell to stay engaged.

SNAP-CAR welds the adaptor on with a covalent bond — the receptor and adaptor become one piece. Signaling holds, and the cell stays lethal even against low-abundance targets.

Tumor cellAntigenAdaptorReceptorCAR-T cellSwitchable CARAffinity bond · reversibleSIGNALSNAP!Tumor cellAntigenAdaptorSNAP-CARSNAP-CAR-TSNAP-CARCovalent bond · lockedSIGNAL

04 — Our Roadmap

01
Complete

Platform licensing & integration

The universal SNAP-CAR adaptor platform is licensed and integrated. One manufactured T- or NK-cell product, redirected by swappable adaptors across liquid and solid tumors.

02
Underway

Preclinical platform optimization

IND-enabling optimization of the platform, establishing preclinical efficacy and proof of concept ahead of the clinic.

03
2027

IND submission

Filing the Investigational New Drug application. A successful submission clears SNAP-CAR into first-in-human study.

04
Phase 1

First patient dosed

The Phase 1 trial opens and the first patient is dosed with a SNAP-CAR product.

05
Phase 1+

Dose escalation & platform expansion

Dose escalation with safety and PK/PD assessment, generating preliminary efficacy and biomarker data, while expanding the platform to new targets and indications.

Team

Experienced leaders.

Deep expertise in oncology drug and cell therapy development, business strategy, and operational excellence.

Dave Mehalick

Dave Mehalick

Co-Founder, President & CEO

30 years across healthcare, IT, finance, and capital markets leadership.

Brian Cogley

Brian Cogley

CFO

15+ years in life sciences, pharmaceutical finance, and corporate strategy.

Dan Yerace

Dan Yerace

Co-Founder & VP of Operations

10+ years spanning pharmaceutical operations, supply chain, and business development.

Christine Sheehy

Christine Sheehy

VP of Compliance & Corporate Secretary

30 years leading finance, operations, and global systems for life sciences.

Lara Ionescu Silverman, PhD

Lara Ionescu Silverman, PhD

VP of CMC

10+ years advancing gene and cell therapy CMC and development.

Partner with us to make cell therapy programmable.

We’re always looking to connect with collaborators, investors, and future team members.