Clinical trial enrollment crisis threatens billions in revenue and patient access
Clinical trials are struggling with enrollment, with about 80% missing timelines and less than 5% of eligible adult cancer patients participating.
Delays have huge financial impact; each day a phase‑3 oncology trial is delayed can cost $600,000‑$8 million, and the industry loses an estimated $50 billion annually.
At the DPHARM conference in Boston, biopharma leaders highlighted site capacity as a key bottleneck, noting that many U.S. sites are already saturated.
The shortage of trial sites and the difficulty recruiting a patient pool that reflects real‑world demographics were identified as major contributors to the enrollment shortfall.
This writeup was produced by pharmadog from original reporting by Fierce Biotech.
Original headline: “DPHARM: How to address the clinical trial enrollment crisis?”
read at Fierce Biotech ↗
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