Lurbinectedin: First Approval
- PMID: 32816202
- DOI: 10.1007/s40265-020-01374-0
Lurbinectedin: First Approval
Abstract
The oncogenic transcription inhibitor lurbinectedin (ZEPZELCA™) is being developed by PharmaMar as a treatment for various cancers. The drug has been granted orphan drug status for the treatment of small cell lung cancer (SCLC) by regulatory authorities in multiple countries worldwide and was approved in the USA in June 2020 for the treatment of adult patients with metastatic SCLC with disease progression on or after platinum-based chemotherapy. The US FDA and international regulators, including the Australian Therapeutic Goods Administration, are collaborating on the review of lurbinectedin under the Project Orbis initiative. Clinical investigation in other solid cancers is ongoing. This article summarizes the milestones in the development of lurbinectedin leading to this first approval for the treatment of metastatic SCLC.
References
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- PharmaMar. Oncology pipeline. 2020. https://pharmamar.com/science-and-innovation/oncology-pipeline/?lang=en . Accessed 6 Jul 2020.
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- PharmaMar. The U.S. Food and Drug Administration (FDA) has granted orphan drug designation to PharmaMar's lurbinectedin [media release]. 3 Aug 2018. https://www.pharmamar.com .
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