{ "meta": { "data_length": 1, "message": "Statement id stmt:hc:rybrevant:2:0 retrieved successfully", "request_url": "https://api.moalmanac.org/statements?statement_id=stmt%3Ahc%3Arybrevant%3A2%3A0", "status": "success", "status_code": 200, "timestamp_elapsed": 0.00257, "timestamp_received": "2026-10-16T23:58:44.692163+00:00Z", "timestamp_returned": "2026-10-16T23:58:44.694733+00:00Z", "trace_id": "38b6bad8-3298-4cff-a5e1-dc80fdad5bbc" }, "service": { "github": "https://github.com/vanallenlab/moalmanac-db", "name": "Molecular Oncology Almanac", "license": "GPL-2.0", "release": "draft", "url": "https://moalmanac.org", "last_updated": "2026-08-02" }, "data": [ { "id": "stmt:hc:rybrevant:2:0", "type": "Statement", "description": "Health Canada approved amivantamab as monotherapy for the treatment of adult patients with locally advanced or metastatic NSCLC with activating EGFR Exon 20 insertion mutations whose disease has progressed on or after platinum-based chemotherapy.", "contributions": [ { "id": "ctrb:vanallenlab:2024-10-30:0", "type": "Contribution", "description": "Initial access of FDA approvals", "date": "2024-10-30", "contributor": { "id": "agent:user:vanallenlab", "type": "Agent", "agentType": "contributor", "name": "Van Allen lab", "description": "Van Allen lab, Dana-Farber Cancer Institute" } } ], "reportedIn": [ { "id": "doc:hc:rybrevant", "type": "Document", "documentType": "Regulatory approval", "name": "Rybrevant (amivantamab-vmjw) [product monograph]. 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