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RESEARCH GUIDE

Protein Degradation: Technologies, Drug Programs, and Services

Targeted Protein Degradation / PROTAC

This guide organizes companies and updates by PROTACs, molecular glue degraders, and other degradation approaches. Use the target, lead program, and development stage to distinguish mechanistic research, clinical development, and services offered to clients.

Questions to ask first

  • Which degradation approach does the lead program use, and what target and mechanism have been disclosed?
  • In which experimental systems or patient populations were degradation, selectivity, and disease-related outcomes observed?
  • Does the company develop its own pipeline or provide discovery, testing, delivery, or CMC services, and is the deliverable clearly defined?

Key terms

PROTAC
The heterobifunctional degrader category in this map, classified separately from molecular glue degraders and other approaches.
Molecular glue degrader
A distinct degradation category in this map, rather than a label applied to every PROTAC program.
CMC services
Development work addressing chemistry, manufacturing, and controls, assessed separately from drug discovery and clinical efficacy.

Evidence and scope

Technology categories support navigation; they are not ratings of efficacy or technical superiority. Cellular degradation does not establish clinical benefit, and starting a trial does not establish a positive outcome. Verify platform capabilities separately from the progress of individual drug programs.

Technology snapshot: 2026-10-31 · Research methods

Recent developments

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Nature Materials

In situ CAR engineering and nanoparticle-mediated TREM2 degradation for macrophage reprogramming in malignant ascites

A Nature Materials study describes mRNA-loaded LNPs that reprogram tumor-associated macrophages into Claudin18.2-targeting CAR macrophages. The lipid formulation also promotes TREM2 internalization and degradation, reshaping immune responses. The original abstract reports tumor suppression and longer survival with PD-1 blockade in mice, plus ex vivo patient-sample findings. These findings do not demonstrate clinical efficacy in treated patients.

Frontiers in Pharmacology

Review assesses the safety limits and translational gaps of MCL-1 degradation strategies

A Frontiers in Pharmacology review compares direct MCL-1 inhibition with approaches that reduce its abundance, including transcriptional interventions and targeted degradation. The original abstract highlights limited single-agent activity and cardiac safety concerns with inhibitors, while positioning degradation as an unvalidated clinical strategy. Biomarker-guided combinations and dynamic BH3 profiling are discussed; this review does not report a new clinical trial.

Evommune and Hinova / Business Wire

Evommune licenses Hinova's VAV1 molecular glue degrader outside Greater China

Evommune licensed EVO570, formerly HC118, from Hinova for development and commercialization outside Greater China. Upfront consideration totals $30 million: $20 million cash and $10 million in pre-funded warrants. Additional development, regulatory, and commercial milestones could reach approximately $1.1 billion, plus royalties. Phase 1 was expected to begin shortly; the announcement does not establish human efficacy.

Companies in this field 74

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The first six companies in this field’s editorial order, not a separate selection or capability ranking. The full directory uses the same data and order.

Arvinas

On 2026-05-01, FDA approved vepdegestrant for certain ESR1-mutated ER+/HER2- advanced breast cancers. In August, the company reported completion of a global license to Rigel and expected future data from three Phase 1 programs.

Protein degradation / PROTAC

Kymera Therapeutics

The 2026-10-29 announcement places KT-621 in Phase 2 for AD and asthma and reports Phase 1 healthy-volunteer results for KT-579. Sanofi is advancing KT-485 in Phase 1; Gilead is preparing a KT-200 CDK2 molecular glue IND.

Protein degradation / PROTAC

Gilead Sciences

Gilead's pipeline updated 2026-10-29 lists GS-6791 as a Phase 1 IRAK4 degrader for inflammatory diseases. Nurix's 2026-10-05 announcement confirms its oral route and clinical status.

Protein degradation / PROTAC

Novartis

An original Phase 1 DKY709 abstract at AACR 2026 describes an oral IKZF2 molecular glue and reports human pharmacodynamic, PK, and preliminary efficacy data through 2024-09-05.

Protein degradation / PROTAC

Merck & Co. / MSD

MSD's website records joint clinical development of an MGD candidate with Degron on 2026-05-21. Original MSD / Proxygen announcements describe a multi-target molecular glue collaboration. C4's 2026 SEC filing states that MSD's DAC agreement ended in November 2025.

Protein degradation / PROTAC

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