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ClinicalIntelPulse Trial Brief
x402
ClinicalIntelPulse Trial Brief is a paid API for AI agents from clinicalintelpulse.theaslangroupllc.com, paid per call via x402, $0.1/call, status unknown (last checked 2026-09-15).
Retrieves a comprehensive deep-dive profile of a specific ClinicalTrials.gov study by NCT ID, including trial design, endpoints, enrollment, sponsor, and publications.
Price / call$0.1
Success—
StatusUnknown
How this service works
Clinical trial deep dive by NCT ID — full trial design, primary/secondary endpoints, enrollment status and countries, sponsor, recruitment criteria, outcomes and publications for any ClinicalTrials.gov study. For research and biotech agents.
Output
A structured profile of the clinical trial including: trial design and phase, primary and secondary endpoints, current enrollment status and target enrollment numbers, list of participating countries, sponsor and collaborator names, inclusion/exclusion recruitment criteria, outcome measures, and linked publications.
Example use cases
Example prompt
“Pull the full trial brief for NCT04280705 — I need the trial design, primary and secondary endpoints, enrollment status, recruiting countries, sponsor, and any published outcomes.”
Technical details
Endpoint
GEThttps://clinicalintelpulse.theaslangroupllc.com/api/clinical/trial-briefWhen to prefer
Use this endpoint when you need a deep, structured profile of a single known clinical trial and already have its NCT ID. It is ideal for research agents, biotech analysts, and competitive intelligence workflows that need granular trial-level data including endpoints, recruitment details, and publications — rather than a broad disease-level landscape view.
Side effects
- Invalid or malformed NCT ID returns a 400 or not-found error
- NCT ID not yet indexed in ClinicalTrials.gov returns empty or null result
- Trial record has minimal data (e.g. newly registered study) resulting in sparse output
- Payment authorization failure via x402 protocol returns 402
- Rate limiting or upstream ClinicalTrials.gov API downtime causes timeout
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Output
Schema · Response
{
"type": "json",
"example": {
"design": {
"arms": [
"Tiragolumab + Atezolizumab + Carboplatin/Paclitaxel",
"Placebo + Atezolizumab + Carboplatin/Paclitaxel"
],
"masking": "Double-Blind",
"allocation": "Randomized",
"study_type": "INTERVENTIONAL",
"primary_purpose": "Treatment"
},
"endpoints": {
"primary": [
"Progression-Free Survival (PFS)",
"Overall Survival (OS)"
],
"secondary": [
"Objective Response Rate",
"Duration of Response",
"Safety/Tolerability"
]
},
"enrollment": {
"actual": 534,
"planned": 534,
"countries": [
"United States",
"Spain",
"Germany",
"Japan",
"Australia"
]
},
"interventions": [
{
"name": "Tiragolumab",
"role": "Anti-TIGIT immune checkpoint inhibitor",
"type": "DRUG"
}
],
"query_summary": {
"nct_id": "NCT04368728",
"retrieved_from": "ClinicalTrials.gov v2 API"
},
"trial_identity": {
"phase": "PHASE3",
"title": "A Study of Tiragolumab in Combination With Atezolizumab and Chemotherapy Versus Placebo in Untreated Locally Advanced Unresectable or Metastatic NSCLC (SKYSCRAPER-01)",
"status": "COMPLETED",
"sponsor": "Hoffmann-La Roche",
"start_date": "2019-06",
"primary_completion": "2022-12"
},
"outcome_summary": "SKYSCRAPER-01 failed to meet primary PFS endpoint (HR 0.93). Significant negative readout for anti-TIGIT in NSCLC.",
"regulatory_implications": "Setback for Roche tiragolumab program. Broader TIGIT class facing headwinds."
}
}Tags
x402
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