The startup operates an independent Site Management Organization that conducts clinical trials by identifying, recruiting, and retaining patients at dedicated research sites. This service enables Contract Research Organizations and pharmaceutical companies to efficiently match patients with appropriate trials across various therapeutic areas.
Funding
$14.4M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Pharmaceutical companies and Contract Research Organizations (CROs) face challenges in efficiently identifying, recruiting, and retaining patients for clinical trials, leading to delays and increased costs in drug development. Traditional recruitment methods often struggle to reach diverse patient populations and maintain engagement throughout the trial duration.
Solution
Panthera Bio operates as an independent Site Management Organization (SMO), specializing in conducting clinical trials across a network of dedicated research sites. By focusing on patient recruitment and retention, Panthera enables pharmaceutical companies and CROs to accelerate clinical breakthroughs. Panthera's streamlined start-up processes reduce the time to first patient enrollment, while targeted recruitment strategies enhance retention and minimize dropouts. The company's model combines clinical precision with patient-focused care, ensuring high-quality data and a seamless collaboration from start to finish.
Target Audience
Panthera Bio serves pharmaceutical companies, biotech firms, and Contract Research Organizations (CROs) seeking to optimize patient recruitment and retention for clinical trials.
Features
- Dedicated clinical trial sites with comfortable surroundings and accessibility via public transport and road
- Sample processing laboratories managed by qualified technical staff
- GCP-trained professional staff with experience in running clinical trials and providing timely, accurate data
- Streamlined contracting and submission process, enabling recruitment to start sooner
- Innovative patient outreach and pre-screening model to recruit more patients while reducing screening visits
- Experienced investigators across a range of therapeutic areas, including cardiovascular disease, MASH, Alzheimer’s, and oncology
- Operational and quality excellence model ensuring consistency across all sites and data integrity
- eSource implementation project to modernize clinical trial processes and enhance data management
- Bespoke Digital Patient Pathway to enhance patient engagement and recruitment