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

Browse all channel updates →
Amphista Therapeutics / Business Wire

Amphista previews BRD9 degradation findings and BRAMLIE trial design at ASH

Amphista announced an ASH oral presentation on AMX-883-mediated BRD9 degradation, describing disruption of hematopoietic transcriptional programs, myeloid differentiation, and reduced leukemic stem-cell frequency in experimental work. A separate abstract outlines the ongoing Phase 1 BRAMLIE study in AML and high-risk myelodysplastic syndrome. The announcement does not establish clinical efficacy for AMX-883.

Proceedings of the National Academy of Sciences / PubMed

Bispecific protein drives dual receptor degradation in mouse eye-disease models

A PNAS study reports RHV, a tetravalent bispecific protein designed to internalize and lysosomally degrade VCAM-1 and VEGFR on pathological vessels. The original abstract describes activity in mouse choroidal neovascularization models, including efficacy comparable to aflibercept at one-quarter of the molar dose. This is preclinical extracellular receptor degradation, distinct from an intracellular small-molecule PROTAC.

Selected company previews

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

Nurix Therapeutics

The 2026-10-12 announcement reports the first participant enrolled in Phase 3 DAYBreak CLL-306. NX-5948 is an oral, brain-penetrant BTK degrader. The company also reported collaboration progress with Roche, Gilead, Pfizer, and Sanofi.

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

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