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Engineering the Next Generation of Small-Molecule Medicines

CRAFT Therapeutics

An AI-enabled precision prodrug company using the ALX Engine to transform established small-molecule drugs into differentiated assets designed to overcome clinical limitations.

Why ALX Matters

ALX creates structurally distinct small-molecule successor drugs before LOE closes. Pharma teams use ALX to protect franchises, differentiate pipeline assets, and unlock new commercial life for existing small molecules.

ALX compounds are new chemical entities (NCEs) — not reformulations.

CRAFT = Chemically Re-Architected Functional Therapeutics

One Platform, Multiple Value Layers

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Better Products

Engineered therapeutics with improved safety, pharmacokinetics, and tissue distribution relative to the originator compound.

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New Composition-of-Matter IP

Each ALX construct is a structurally distinct, new chemical entity, generating independent intellectual property protection.

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Extended Commercial Life

New IP coverage and differentiated clinical profiles extend the commercial runway beyond loss-of-exclusivity timelines of the originator.

Existing Drugs Have Fixable Limitations

Approved small-molecule drugs carry well-documented limitations that create a clear opportunity for engineering-led improvement.

01

Safety Liabilities

On-target and off-target toxicity

02

PK Limitations

Suboptimal ADME profiles

03

Tissue Distribution Challenges

Poor selectivity for target tissue

04

Dosing Burden

Frequent dosing requirements

05

Loss of Exclusivity

Patent cliffs eroding commercial value

ALX Solution: A Modular Product-Profile Engineering Architecture

ALX is a modular architecture that combines three defined components to create structurally distinct, new therapeutic entities, not reformulations.

A

Activator

Validated Drug

A clinically validated small-molecule drug as the active foundation.

L

Linker

Reversible & Controlled

Reversible linker enabling controlled release and modulated pharmacokinetics.

X

Effector

Tunable Domain

Tunable effector domain that modulates the overall therapeutic profile.

ALX Feasibility Criteria

  • ✓
    Small-molecule drugs with clean conjugation handles
  • ✓
    CRO-available bioassays
  • ✓
    Biologically triggered linker compatibility (Val-Cit, amino acids, sugars, metabolites)
  • ✓
    Small-molecule X-domains only (no peptides, proteins, polymers)

A Large, Repeatable Opportunity Universe

The addressable market for ALX is substantial, spanning both marketed drugs and pipeline candidates.

Marketed TAM
$310B–$390B
  • ~70–80% of 3000+ marketed small molecules are structurally amenable
  • Targets approved drugs with established safety and commercial profiles
Pipeline TAM
$150B–$400B
  • ~5,100–6,400 pipeline candidates applicable
  • Spans early-stage through late-stage development

Multiple Paths to Value Creation

Pharma Partnerships

Licensing

Co-Development

Internal Development

About CRAFT Therapeutics

Building next-generation small-molecule medicines using the patent-pending ALX architecture.

For Pharma, CROs, and CDMOs

CRAFT partners with pharma IR teams, CROs, and manufacturing organizations to evaluate ALX feasibility, generate ALX variants, and license ALX molecules for development and manufacturing.

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Partnership Inquiries

For pharma, CRO, CDMO, and manufacturing partners interested in ALX evaluation or licensing, we’d be happy to connect.