Registry analysis reveals early-phase dominance and high attrition in antibody-drug conjugate trials, highlighting the need for biomarker-guided late-phase development.
Antibody-drug conjugates (ADCs) represent a breakthrough in tumor-targeted therapy, showing promise in both solid tumors and hematological malignancies. By 1 September 2025, more than 370 ADC candidates had entered clinical development, 17 unique products had received at least one regulatory approval worldwide, and more than 150 candidates had been discontinued. This study analyzes 3,077 ADC trials from Citeline Trialtrove, revealing that most trials are concentrated in the United States and China. At the data cutoff, 35% of trials were ongoing and 12% were classified as terminated in Trialtrove. ADC trials primarily focused on solid tumors, with brentuximab vedotin, disitamab vedotin, and gemtuzumab ozogamicin being the most frequently investigated agents. Early-phase trials predominated, whereas Phase III and IV trials were less frequent. EGFR, BRCA1, and TP53 were frequently recorded across trial-design and outcome-related fields. Future research should focus on advancing later-phase trials, refining safety and efficacy, and exploring new therapeutic targets with continued biomarker integration.
No takes yet. Share an insight, caveat, or question.
Hu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: