Clinical trials
Study design, indications, phase, medicinal products, eligibility, endpoints, recruitment, countries and timelines.
We document all details about every clinical trial with medicinal products approved in the EU since 2021. Every single trial, with all information collected and structured.
Bring trial evidence, CRO experience, research sites, principal investigators, protocols and documents into your AI workflow through TrialAgents MCP.
https://mcp.trialagents.com/research/mcpAlready have an account or saved projects?
Open your projectsMove from a research question to comparable trials and the organizations, people and documents behind them.
Study design, indications, phase, medicinal products, eligibility, endpoints, recruitment, countries and timelines.
Organizations linked to trials, their recorded roles and the underlying study evidence. Compare relevant experience for your project.
Trial locations and site participation, connected to the trials that demonstrate their research experience.
Investigators, their trial participation and associated research sites, with evidence for your selection.
Available protocol text and trial documents for detailed questions about design, eligibility, endpoints and study conduct.
Connected records that agents can search, filter, compare and explain, with source evidence and clear distinctions between reported facts and analysis.
Each research selection supports up to 1,000 trials. The public preview shows up to 10 trials, sites, principal investigators and CROs each. Saving projects requires a connected account. Full matching lists and other paid capabilities depend on your account access. Connecting an account alone does not unlock paid access.
Ask for comparable trials, experienced CROs, sites or investigators. Refine the cohort by your study's criteria.
Explore trial profiles, compare selections, review available protocol and document content, and trace findings back to the evidence.
Save a project, revisit your selection and create Custom views such as reports, tables, charts and dashboards using your permitted data.
Try: “Find EU trials relevant to my Phase II oncology study and compare the CROs, sites and investigators with matching experience.” Then ask about their protocols, eligibility criteria, endpoints or timelines.
Agents should discover the live tool schemas, respect access limits and distinguish missing evidence from negative findings. Trial participation and recorded roles do not establish provider performance.
TrialAgents documents all details about every clinical trial with medicinal products approved in the EU since 2021, with all information collected and structured. The research connection brings that evidence into supported agent workflows. Individual document retrieval depends on document availability and account access.
Open your projects in TrialAgents Intel. If needed, you will be asked to log in through the existing TrialAgents sign-in flow.
This is the human-readable documentation page. Configure your agent with https://mcp.trialagents.com/research/mcp. Existing integrations using the legacy endpoint https://mcp.trialagents.com/mcp remain supported; do not change an existing integration's endpoint without checking its tool requirements.
TrialAgents uses its existing OAuth connection flow. Your client requests authorization when required. Email hints help fill in the login form; they do not authenticate a user or grant access to another account's projects.