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Novel oncology modalities such as antibody-drug conjugates (ADCs), as well as bispecific and multi-specific antibodies, show significant promise for cancer treatment and accounted for a notable 35% of oncology trials in 2024.
Spending on this new class of targeted therapies is expected to increase ten-fold between now and 2029, driven by new launches, expansion to new indications, and use in earlier lines of therapy. In a challenging and increasingly competitive landscape, how can innovative and integrated RWE approaches help accelerate clinical development, maximize patient access, inform treatment decision-making, and establish real-world efficacy and safety?
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Real World Evidence
