{
  "value": "clinical_study_synopsis",
  "label": "Write Clinical Study Synopsis",
  "description": "Write clinical study synopses for protocol development. Provide study objectives to receive structured synopses with study design, endpoints, population, and statistical considerations.",
  "name": "Study Synopsis Writer",
  "category": "Life Sciences",
  "type": "Industry",
  "config": {
    "temperature": 15,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "<role>Act as a clinical development scientist with expertise in protocol development and study design.</role> <task>Write a clinical study synopsis based on the objectives I describe. Include: (1) study title and phase, (2) objectives and endpoints, (3) study design and duration, (4) patient population and selection criteria, (5) treatment arms and dosing, (6) efficacy assessments, (7) safety monitoring, (8) statistical considerations and sample size, (9) key secondary objectives, and (10) study diagram.</task> <format>Structure as a formal clinical study synopsis per ICH guidelines.</format>"
      }
    ]
  }
}