Espero Health provides a comprehensive platform for managing complex patient care pathways, focusing on oncology and specialty therapeutics. The system integrates clinical data and workflow automation to streamline treatment coordination across multidisciplinary teams. This results in improved adherence to evidence-based protocols and enhanced patient navigation through intricate care journeys.
Funding
Funding not disclosed
Founders
Product
Problem
Clinical trial protocol development is often a fragmented, manual process involving multiple stakeholders and systems, leading to inefficiencies, delays, and increased costs. The lack of seamless data exchange between protocol design and downstream systems, such as Electronic Data Capture (EDC) and Interactive Response Technology (IRT), further exacerbates these challenges.
Solution
Espero offers a digital-first eProtocol platform designed to streamline and accelerate clinical trial protocol development. The platform centralizes protocol authoring, facilitates collaborative workflows, and enables digital data flow (DDF) to downstream systems. By leveraging machine learning and advanced analytics, Espero automates tasks such as protocol template pre-population, insight generation from historical trials, and dynamic document generation (e.g., ICF, IB, CSR, SAP, and Lab Manuals). The platform also supports compliance with ICH M11 standards and automates FDA submissions, reducing manual effort and improving data quality.
Target Audience
Espero targets pharmaceutical companies, biotech firms, and clinical research organizations (CROs) seeking to improve the efficiency, quality, and speed of clinical trial protocol development.
Features
- Centralized platform for collaborative protocol authoring with audit trails and version control
- Data-driven protocol design using machine learning to analyze historical clinical trials and provide insights
- Automated generation of study documents, including ICF, IB, CSR, SAP, and Lab Manuals
- Streamlined FDA submission process compliant with ICH M11 standards
- Digital Data Flow (DDF) integration with EDC, IRT, and other downstream systems for automated eCRF builds
- Real-time feedback from sites and patient advocacy groups to optimize protocol design
- Cost forecasting tools for feasibility and trial planning