Induced-proximity therapeutics have emerged as a significant modality in drug discovery, enabling the selective elimination of disease-causing biomolecules by harnessing endogenous degradation, which drives the growth of the market.
Induced-proximity drug discovery represents a shift from classical occupancy-driven pharmacology to approaches that control protein function by enforced protein–protein interactions. Continued innovation in these modalities is expected to significantly impact drug discovery by allowing selective and durable modulation of proteins earlier considered undruggable. Induced proximity is a significant approach for regulating proteins via loss or gain of function. This innovative mechanism employs proximity-inducing molecules to bring proteins or nucleic acids to modulate the function of a target and the related cellular technology. Major biotech companies have leveraged the therapeutic potential of the encouraged proximity strategy to develop drugs against several diseases.
The global induced proximity molecules market size was estimated at USD 4.2 billion in 2025 and is predicted to increase from USD 4.99 billion in 2026 to approximately USD 23.32 billion by 2035, expanding at a CAGR of 18.7% from 2026 to 2035.
Induced proximity has changed into a versatile platform with the potential to transform drug discovery. Scientists developed a novel strategy using molecules called Group-transfer chimeras for inducing proximity (GRIPs). Increasing the induced-proximity paradigm beyond proteins, researchers have recently developed small-molecule chimeras that target RNA for degradation. These are known RIBOTACs, heterobifunctional or multispecific molecules that bind an RNA of interest and concurrently recruit an RNase to cleave that RNA. GRIPs avert rebound signalling, initiate PTM crosstalk, and clear pathogenic PTMs in cellular systems.
The top five companies in this group dominate the U.S. induced proximity molecules market. Meanwhile, Arvinas, the leader in PROTAC drug discovery, is taking the most advanced assets into clinical trials. C4 Therapeutics it is focusses in TPD to create novel medicines for cancer and neurodegenerative diseases. Monte Rosa Therapeutics (MA) is progressing precision medicine-based molecular glue degraders. Magnet Biomedicine, a molecular glue organization that evolved from stealth to expand the scope of glue medicines. Kayak Therapeutics, it develops covalent, induced proximity-driven therapies targeting E3 ubiquitin ligases.
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