LIVE MARKETS-Targeted cancer therapies market set to reach $31 billion by 2030
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TARGETED CANCER THERAPIES MARKET SET TO REACH $31 BILLION BY 2030
The market for antibody-drug conjugates (ADCs), a lucrative class of targeted cancer therapies often described as "guided missiles", is projected to reach $31 billion by 2030, based on currently approved drugs, according to analysts at brokerage TD Cowen.
ADCs are designed to selectively kill tumor cells while sparing healthy ones, offering a more targeted approach than traditional chemotherapy, which can harm both.
The innovative class of cancer treatments combine targeted therapy and chemotherapy to deliver directly to diseased cells, acting as a "silver bullet" to limit systemic exposure to toxic drugs, the analysts noted.
The field has made notable progress in recent years, with 13 approved therapies across different types of cancer amounting to a $11.5 billion market in 2024. However, the first generation therapies face certain drawbacks of toxicity and resistance.
The focus is now shifting to questions regarding selection of target, drug payload, and conjugation technology, and development strategy.
The market potential could exceed current projections as new ADCs expand into more cancer types, and move into earlier stages of treatment.
On the other hand, bispecific antibody drug conjugates (bsADC) are an emerging therapeutic approach that presents advantages over traditional ADCs, according to GlobalData.
They use bispecific antibodies that bind to two different targets, making treatments more precise and reducing side effects.
There are four therapies currently in late-stage development for East Asian markets. Systimmune and Bristol Myers Squibb’s BMY.N izalontamab brengitecan, Shanghai JMT-Bio Technology’s JSKN-003, and Chia Tai Tianqing Pharmaceutical Group’s TQB-2102 are focused on China, whereas Amgen’s AMGN.O maridebart cafraglitide targets the Japanese market.
"This regional concentration aligns with the dominance of Chinese companies in ADC development and suggests that the first bsADC approval may occur in Asia, rather than in the US or EU," said Jasper Morley, Pharma Analyst at GlobalData.
(Sriparna Roy)
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