PD-L1 Protein Degrader

Targeting PD-L1 Evasion

PD-L1 is a protein that plays an important role in regulating the immune system, but some cancer cells take advantage of this natural mechanism to escape immune detection. Our lead compound, NDL2, is an optimized bicyclic peptide designed to selectively degrade disease-associated nuclear PD-L1 protein and restore the body’s natural anti-tumor immune response.

Pipeline

PD-L1 Protein Degrader
Study / Indication Preclinical Phase 1 Phase 2 Phase 3 Market Sponsor
Advanced Solid Tumors
Preclinical

Development Stage

Preclinical; IND expected in 2H 2027

Lead Indications

Solid tumors that are traditionally refractory to immunotherapy, such as metastatic breast cancer and colorectal cancer

Mechanism of Action

Recruiting Cellular Degradation Machinery

NDL2 selectively targets nuclear PD-L1 protein pools that are enriched in cancer cells and inaccessible to conventional checkpoint inhibitors. By recruiting the cell’s natural degradation machinery, it promotes the clearance of these intracellular tumor-specific PD-L1 protein, offering a mechanism to enhance immune-mediated tumor control.

We Opened a New Frontier

Advancing within Scientific Categories

Targeted Protein Degradation (TPD) therapies opened a new frontier for treating cancer by exploiting naturally occurring protein degradation pathways to disrupt critical cellular processes.

As a first-in-class therapy, NDL2 is advancing within a new scientific category, PD-L1 degradation, with no other compounds yet in clinical development.

Upcoming Advancements

  • Initiate IND-enabling studies
  • Integrate a clinical liquid biopsy to enable patient stratification, real-time monitoring, and personalized treatment optimization
  • Launch PD-L1 Degrader and NDL2 awareness campaign through abstracts, manuscripts, videos, and medical congress presentations

Ongoing Clinical Trials

Learn more about how our transformative therapies are progressing through clinical development by exploring our current clinical trials.

View Our Clinical Trials

Shifting Innovation

The future of targeted oncology lies not simply in blocking cancer signaling, but in reprogramming the biology that enables cancer to survive, adapt, and spread.

View Our Technology

Our Research in Focus

Explore our posters and publications to access our latest scientific data, clinical insights, and contributions to advancing oncology research.

View Our Posters & Publications

Discover Our Other Candidates

Paxalisib

Paxalisib is a potentially best-in-class, oral, brain-penetrant dual P13K/mTOR inhibitor designed to reprogram cancer biology through precision pathway inhibition, restoring anti-tumor immunity and overcoming therapeutic resistance.

Learn About Paxalisib

SETDB1 Inhibitor

We are developing MSETC, a first-in-class therapeutic targeting disease-associated SETDB1 complex, to restore anti-tumor immune signaling and overcome mechanisms of immune evasion.

Learn About SETDB1 Inhibitor

EVT801

EVT801 is an oral, highly selective small-molecule inhibitor of VEGFR-3 designed to modulate lymphangiogenesis and metastatic spread.

Learn About EVT801