The U.S. healthcare contract research organization market is expected to grow from $15.01 billion in 2025 to $29.68 billion by 2034, driven by increasing R&D investments and technological advancements.
Clinical trial sites are struggling with technological overload, with 60% of sites managing over 20 overlapping software systems, creating significant administrative burden for investigators.
Syneos Health successfully integrated 20/20 Onsite's Mobile Clinical Suite to conduct comprehensive eye safety assessments for over 65 patients in a Phase 1 clinical trial.
The U.S. cell and gene therapy bioanalytical testing services market is projected to grow from $181.73 million in 2025 to $349.29 million by 2034, representing a CAGR of 7.53%.
Syneos Health is hosting a forward-looking webinar on January 28th exploring emerging healthcare trends, focusing on digital health, biotechnology advances, and personalized medicine solutions.
The global clinical trial outsourcing market is projected to grow from $43.1 billion in 2025 to $91.2 billion by 2034, representing a robust CAGR of 7.46% as pharmaceutical companies increasingly rely on CROs to streamline research processes.
The FDA has cleared CytoDyn's phase 2 trial of leronlimab in relapsed/refractory microsatellite stable colorectal cancer (MSS CRC).
CytoDyn has received FDA clearance to begin a Phase II oncology trial evaluating leronlimab in patients with relapsed/refractory microsatellite stable colorectal cancer.
CytoDyn has obtained FDA clearance to initiate a Phase II trial evaluating leronlimab in patients with relapsed/refractory microsatellite stable colorectal cancer.
CytoDyn has obtained FDA clearance to initiate a Phase II oncology trial evaluating leronlimab in patients with relapsed/refractory microsatellite stable colorectal cancer.