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Bringing Proteins Together to Reshape Medicine

Rapafusyn is pioneering RapaGluesTM – a unique modality of non-degrading molecular glues for targets previously considered intractable

Bringing Proteins Together
to Reshape Medicine

Rapafusyn is pioneering RapaGluesTM – a unique modality of non-degrading molecular glues for targets previously considered intractable

Bringing Proteins Together
to Reshape Medicine

Rapafusyn is pioneering RapaGluesTM – a unique modality of non-degrading molecular glues for targets previously considered intractable

We are driven by the desire to create novel therapies for underserved patients.

Our Science: RapaGlues

Nature has created multiple FKBP12 binding medicines (FK-506, Rapamycin). Rapafusyn has novel technology to extend nature’s mechanism to many previously undruggable targets.

RapaGlues are cell permeable macrocycles that bring the abundant intracellular chaperone protein FKBP12 in proximity with a target of interest

Graphic describing the RapaGlue Mechanism of Action

FKBP12 forms neo-protein-protein interactions to block a target’s native function

Benefits of RapaGlues

Desirable Drug-Like Properties Icon
  • Permeability
  • Exquisite Selectivity
  • High Tunability
  • Oral Delivery
Ability to Tackle Previously Undruggable Target Icon

RapaGlues can be positioned to target nearly any intracellular protein including:

  • Protein-Protein Interactions
  • Intracellular domains of transmembrane proteins
  • Transcription Factors
  • Enzymes and Ligases
Validated Approach and Modality Icon
  • Multiple approved drugs utilize same FKBP binding mechanism (e.g. FK-506,
    Rapamycin and analogs)
Design element
Design element

Broad Utility of the Platform

The Rapafusyn platform of non-degrading molecular glues demonstrates superior properties in effectively inhibiting a wide range of intracellular and transmembrane targets. Inhibiting PPIs and intracellular domains of transmembrane proteins are targets where our modality may have advantages over other approaches.

Image showing how the RapaGlue:FKBP12 complex can inhibit a wide range of targets.

Our Pipeline

Track the progress we’re making on our internal programs.

Hit Identification Hit to Lead Lead to DC DC to IND
ENT1 Inhibitor
(SLC for Acute Kidney Injury)
ONC-003
(SLC for Oncology)
ONC-005
(GSTPase for Oncology)
ONC-006
(TF for Oncology)
ONC-001
(Immune-Regulatory Ligase for Oncology)
IMM-001
(TF for I&I)
IMM-002
(TNFR1 Specific PPI for I&I)
IMM-003
(TNFR1 Specific PPI for I&I)
Hit

IND
ENT1 Inhibitor
(SLC for Acute Kidney Injury)
 
DC to IND
ONC-003
(SLC for Oncology)
 
Hit to Lead
ONC-005
(GSTPase for Oncology)
 
Hit to Lead
ONC-006
(TF for Oncology)
 
Hit Identification
ONC-001
(Immune-Regulatory Ligase for Oncology)
 
Hit Identification
IMM-001
(TF for I&I)
 
Hit to Lead
IMM-002
(TNFR1 Specific PPI for I&I)
 
Hit to Lead
IMM-003
(TNFR1 Specific PPI for I&I)
 
Hit to Lead

SLC: Solute Carrier (transporter, membrane protein)
TF: Transcription Factor
I&I: Immunology & Inflammation
PPI: Protein-Protein Interaction

Want to Collaborate? Let’s Discuss Partnering Opportunities!

Latest News

September 2nd, 2026|

Rapafusyn Pharmaceuticals to Present at the H.C. Wainwright 28th Annual Global Investment Conference

December 11th, 2025|

Rapafusyn Founder Dr. Jun O. Liu Elected as National Academy of Inventors Fellow

September 4th, 2025|

Rapafusyn Pharmaceuticals Closes Over-Subscribed $44 Million Series A Financing

Contact Us

Want to Collaborate?
We actively pursue partnerships and collaborations to expand and accelerate the development of RapaGlues.

For Partnering Inquiries: partnering@rapafusyn.com

For General Inquiries: contact@rapafusyn.com

Rapafusyn Pharmaceuticals
855 N. Wolfe Street
Baltimore, MD 21205
410-995-8234

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