{ "meta": { "data_length": 1, "message": "Statement id stmt:ema:glivec:5:0 retrieved successfully", "request_url": "https://api.moalmanac.org/statements?statement_id=stmt%3Aema%3Aglivec%3A5%3A0", "status": "success", "status_code": 200, "timestamp_elapsed": 0.002209, "timestamp_received": "2026-10-16T23:30:55.300557+00:00Z", "timestamp_returned": "2026-10-16T23:30:55.302766+00:00Z", "trace_id": "dc251528-8b56-4172-9414-f18ad8b7230c" }, "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:ema:glivec:5:0", "type": "Statement", "description": "The European Medicines Agency (EMA) has authorized imatinib for the treatment of adult patients with advanced hypereosinophilic syndrome (HES) and/or chronic eosinophilic leukaemia (CEL) with a FIP1L1::PDGFRA rearrangement.", "contributions": [ { "id": "ctrb:vanallenlab:2024-10-20:0", "type": "Contribution", "description": "Adding EMA approvals for use to database", "date": "2024-10-20", "contributor": { "id": "agent:user:vanallenlab", "type": "Agent", "agentType": "contributor", "name": "Van Allen lab", "description": "Van Allen lab, Dana-Farber Cancer Institute" } }, { "id": "ctrb:ema:2001-11-07:0", "type": "Contribution", "description": "Indication received approval from the European Commission.", "date": "2001-11-07", "contributor": { "id": "agent:org:ema", "type": "Agent", "agentType": "organization", "name": "European Medicines Agency", "description": "Regulatory agency that approves medicines for use in the European Union." } } ], "reportedIn": [ { "id": "doc:ema:glivec", "type": "Document", "documentType": "Regulatory approval", "name": "Glivec (imatinib) [product information]. 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