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Jazz Pharmaceuticals Announces U.S. FDA Accelerated Approval of Zepzelca™ (lurbinectedin) for the Treatment of Metastatic Small Cell Lung Cancer

Approval represents an important advance for adult patients whose metastatic SCLC has progressed on or after platinum-based chemotherapy Zepzelca is approved

articleJazz Pharmaceuticals PlcJune 15, 20205/company/jazz-pharmaceuticals-plc/news/jazz-pharmaceuticals-announces-us-fda-accelerated-approval-of-zepzelcatm-lurbinectedin-for-the-treatment-of-metastatic-small-cell-lung-cancer
Jazz Pharmaceuticals Announces U.S. FDA Accelerated Approval of Zepzelca™ (lurbinectedin) for the Treatment of Metastatic Small Cell Lung Cancer

About this update from Jazz Pharmaceuticals Plc

[{"type":"text","content":"Approval represents an important advance for adult patients whose metastatic SCLC has progressed on or after platinum-based chemotherapy\n Zepzelca is approved under accelerated approval based on overall response rate and duration of response demonstrated in an open-label, monotherapy clinical trial\n Zepzelca is expected to be commercially available in the U.S. in early July\n Investor webcast on Wednesday, June 17 at 6:15 p.m. EDT\n\n\nDUBLIN, June 15, 2020 /PRNewswire/ -- Jazz Pharmaceuticals plc (Nasdaq: JAZZ) today announced along with its partner PharmaMar (MSE: PHM) that the U.S. Food and Drug Administration (FDA) approved Zepzelca™ (lurbinectedin) for the treatment of adult patients with metastatic small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy.1 Zepzelca was approved under accelerated approval based on overall response rate (ORR) and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.1\nThe FDA approval of Zepzelca is based on monotherapy clinical data from an open-label, multi-center, single-arm study in 105 adult platinum-sensitive and platinum-resistant patients with SCLC who had disease progression after treatment with platinum-based chemotherapy.2 The data, which appeared in The Lancet Oncology May 2020 issue, showed that in patients with relapsed SCLC, Zepzelca demonstrated an ORR of 35 percent and a median duration of response of 5.3 months as measured by investigator assessment (30 percent and 5.1 months respectively, as measured by an independent review committee (IRC)).1 \n\"Small cell lung cancer is a disease with limited treatment options, and the approval of Zepzelca represents an important advance for patients whose metastatic SCLC has progressed on or after platinum-based therapy,\" said Bruce Cozadd, chairman and CEO of Jazz Pharmaceuticals. \"While patients may initially respond to traditional chemotherapy, they often experience an aggressive recurrence that is historically resistant to treatment. Jazz congratulates PharmaMar on the successful development of Zepzelca and we are proud to partner with them to bring this new therapy to the U.S. market, expanding our presence in oncology.\"\nZepzelca will be commercially available in the U.S. in early July...

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