Targeted Protein Degraders
PROTACs and molecular glues are a new therapeutic modality with multiple clinical-trial entries. The session covers ARV-471 (vepdegestrant) in ER+ breast cancer, BMS-986365 in androgen-receptor-positive prostate cancer, KT-474 in autoimmune disease, molecular-glue degraders (cereblon-binders like CC-220 iberdomide), ARV-110 (bavdegalutamide) discontinuation lessons, and the regulatory pathway for degraders. Discussion addresses PROTACs vs molecular glues comparison, hook-effect pharmacology, the catalytic stoichiometry advantage, oral bioavailability challenges, intracellular protein-protein-interaction targets newly accessible, and the IP and patent landscape.
- ARV-471 in breast cancer
- BMS-986365 prostate
- KT-474 autoimmune
- Molecular-glue degraders
- ARV-110 lessons
- PROTACs vs glues
- Hook effect
- Catalytic stoichiometry
Explore the full WCPD 2027 program
- 01Drug Discovery & Design
- 02Clinical Pharmacology
- 03Pharmacogenomics & Precision Medicine
- 04Drug Delivery Systems
- 05Toxicology & Safety Pharmacology
- 06Regulatory Science & Policy
- 07Pharmacovigilance
- 08Biopharmaceuticals
- 09Pharmaceutical Manufacturing
- 10mRNA & RNA Therapeutics
- 11Antibody Engineering
- 12Oligonucleotide Therapeutics
- 13AI for Drug Design
- 14Real-World Evidence
- 15Adaptive Clinical Trials
- 16Pharmaceutical Quality
- 17Generic & Biosimilars
- 18Access & Pricing
- 19Antimicrobial Drug Development
- 20Antiviral Drug Development
- 21Anticancer Therapies
- 22CNS Drugs
- 23Endocrine Drugs
- 24Pediatric Drug Development
- 25Geriatric Pharmacology
- 26Herbal & Natural Products
- 27Drug Repurposing
- 28Orphan Drugs
- 29Combination Therapies
- 30Drug-Drug Interactions
- 31Pharmacoeconomics
- 32Compounding Pharmacy
- 33Hospital Pharmacy
- 35Pharmacovigilance Innovation