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PROTAC Protein Degraders Enter Phase 3 Trials, Targeting 'Undruggable' Proteins

9 months ago1 min read

Key Insights

  • PROTAC protein degraders, designed to target previously 'undruggable' proteins, are now advancing into late-stage clinical trials.

  • These degraders work by inducing proteolysis, offering a novel approach to target proteins lacking traditional active sites for inhibition.

  • The advancement represents a significant milestone in drug development, potentially expanding the range of treatable diseases.

Proteolysis-targeting chimeras (PROTACs) are a novel class of drugs designed to degrade previously 'undruggable' proteins, are now entering phase 3 clinical trials. These proteins, often lacking traditional active sites or being inaccessible to conventional drugs, have long posed a challenge to drug developers.
PROTACs function by inducing proteolysis, a process where the targeted protein is marked for degradation and subsequently removed by the cell's natural machinery. This approach bypasses the need to inhibit or agonize a protein's activity, opening up new therapeutic possibilities.
The advancement of PROTACs into late-stage clinical trials marks a significant milestone in the field. If successful, these trials could pave the way for new treatments for a variety of diseases currently considered intractable due to the limitations of traditional drug discovery methods.
This innovative approach represents a paradigm shift in drug development, potentially expanding the scope of treatable targets and offering new hope for patients with unmet medical needs.
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