Targeted Protein Degradation in Oncology Markets
Targeted Protein Degradation in Oncology: Market Forecast, Competitive Landscape and Strategic Opportunities, 2027–2031
Global forecasts by modality, indication, target, E3 ligase and product, with country and regional breakouts and 12 company profiles.
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Our Take
Targeted protein degradation is about to change hands. Today 98% of the $7.0 billion market is Revlimid, Pomalyst and their generics; by 2031 next-generation degraders account for two-thirds of a $10.7 billion market. CELMoDs hold the myeloma franchise for Bristol Myers Squibb, but the real growth is in PROTAC-type degraders for BTK and the androgen receptor that are still in Phase 3, and the first approved PROTAC, Veppanu, shows that approval alone does not make a commercial success.

Situation Analysis: what is really happening
- The IMiD franchise is going generic. Revlimid and Pomalyst, with their generics, fall from $6.4 billion to $3.4 billion as U.S. generic pomalidomide follows lenalidomide.
- CELMoDs hold myeloma. Zenbexus (iberdomide) won accelerated approval in August 2026 and mezigdomide has an FDA decision in May 2027. Together they reach $3.0 billion and keep myeloma revenue almost flat.
- The growth is in PROTACs still in Phase 3. The BTK degraders BGB-16673 and bexobrutideg and the androgen receptor degrader BMS-986365 drive PROTACs from $8 million to $3.3 billion. Their approval timing is the largest risk to the forecast.
- Big pharma is buying platforms. J&J's $3.05 billion Halda acquisition, Roche's upfront of more than $700 million for bexobrutideg and its October 2026 Defand deal show where large companies expect value.
Company Analysis: who is positioned, who is exposed
- Bristol Myers Squibb: Owns both the IMiD franchise and its replacements, Zenbexus, mezigdomide and BMS-986365, and remains the leader in oncology degraders throughout the forecast.
- Arvinas, Pfizer and Rigel: Veppanu was the first PROTAC approved, but its narrow ESR1-mutated label led Arvinas and Pfizer to license it to Rigel for $70 million upfront.
- Roche: The most active dealmaker, with Nurix's BTK degrader, C4's degrader-antibody conjugates and a new molecular glue deal with China's Defand.
- Nurix Therapeutics: Bexobrutideg, co-developed with Roche, must beat established BTK inhibitors and catch up with BeOne's more advanced BGB-16673.
- Johnson & Johnson / Halda: A $3.05 billion bet on the RIPTAC induced-proximity platform, still early in prostate cancer.
- NATCO Pharma: First with U.S. generic pomalidomide, with shared 180-day exclusivity, and at the front of the IMiD generic wave.
Plus 3 more company profiles covering molecular glue platform companies and big pharma partners.
Questions this report answers
- How fast will Revlimid and Pomalyst revenue fall as generics spread?
- Can CELMoDs replace the IMiD franchise in multiple myeloma?
- Which PROTACs will reach the market by 2031, and how large can they become?
- Will BTK and androgen receptor degraders beat the inhibitors they aim to replace?
- How fast is China moving in degraders and generic IMiDs?
- Is cereblon still the only E3 ligase that matters commercially?
What’s inside
- 161 pages, 23 chapters, 34 tables and 55 figures
- 12 company profiles with technology, pipeline, strategy and risks
- Forecasts 2027–2031 from a 2026 base (actual) year, by modality, indication, target, E3 ligase and product, for 14 countries and regions
- Approved product registry and 2025 sales benchmarks
- Generic erosion of the IMiDs, regulatory pathways, and a China ecosystem chapter
- Delivered as 3 files: full report PDF, Situation Analysis PDF, and Excel workbook of all charts and tables
- Download the Table of Contents (PDF)
See inside before you buy
Get a free sample: the full table of contents plus real pages of analysis, company profiles, tables and charts.
Who buys this report
- Business development and licensing teams: find platform and asset partners and track who leads each modality.
- Investors and equity analysts: model the IMiD generic decline and the timing of next-generation launches.
- Degrader developers: choose the targets, E3 ligases and indications with the most room to grow.
- Generic manufacturers: size the lenalidomide and pomalidomide generic opportunity.
Licences and support
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About the author
Greg Powell, B.Sc., M.B.A., has worked in laboratory testing and management for more than 20 years, with executive training at Harvard Business School and the Burke Institute.