Clinical trials, from protocol to report.
One workspace for the full cycle.
- Plan: protocol draft, endpoints, cohort criteria and statistical analysis plan.
- Start and run: site feasibility, CRFs and monitoring summaries.
- Close: a clinical study report drafted from the final data.
Plan → Start → Run → Close · the cohort fills in
Three agents, one result.
You ask · agents take turns · results arrive cited · you sign off
Reader long-context LLM
Collects prior trials, guidelines and endpoints.
Analyst code model
Works on cohort criteria, sample size and data summaries.
Writer drafting LLM
Drafts the protocol, CRFs, SAP and CSR sections.
What you get back.
Protocol and SAP
Drafted from your study question and sources.
CRFs
Built from the protocol, field by field.
Monitoring summaries
What changed at each site, in plain words.
CSR draft
Sections drafted from the final data.
Common questions.
Does Cytogent run the trial?
No. Your team and your sites run the trial. Cytogent drafts and supports the documents around it. It is a research tool, not a medical device, and it makes no clinical decisions.
Can it work with our study data?
Yes. Study data is added to a project that only your team can see, with owner, editor and viewer roles. Agents work inside that project, and the data never trains shared models.
Who approves the documents?
Qualified people on your team. Every draft goes to review, and each sign-off is written into the project record, so it is always clear who approved what and when.
Works well with.
Regulatory documentation
IND/CTA modules, IVDR technical files and SOPs, structured for reviewer questions.
See this workflowLiterature & evidence
Papers, patents, protocols and registries in one query. Every claim points to its source.
See this workflowIn-silico studies
Screen, simulate and compare before the bench: docking, ADMET, pathway and PK models.
See this workflowBring your next question.
Tell us your field and what you want to do. We set up the workspace around it.
Request access