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Onco360 Selected As The Preferred National Specialty Pharmacy Partner For Karyopharm's Product XPOVIO, A First-In-Class, XPO-1 Inhibitor

Onco360 Selected As The Preferred National Specialty Pharmacy Partner For Karyopharm's Product XPOVIO, A First-In-Class, XPO-1 Inhibitor

Onco360 被选为 Karyopharm 产品 XPOVIO 的首选全国专业药房合作伙伴,XPOVIO 是一款同类首创的 XPO-1 抑制剂
Benzinga ·  03/13 16:38

Onco360, the nation's largest independent Oncology Pharmacy, is now the national specialty pharmacy network partner for Karyopharm's product XPOVIO (selinexor), a first-in-class, XPO-1 inhibitor. XPOVIO is approved in multiple oncology indications, including: (i) in combination with Velcade (bortezomib) and dexamethasone (XVd) in patients with multiple myeloma after at least one prior therapy; (ii) in combination with dexamethasone in patients with heavily pre-treated multiple myeloma; and (iii) in patients with diffuse large B-cell lymphoma (DLBCL), including DLBCL arising from follicular lymphoma, after at least two lines of systemic therapy.

美国最大的独立肿瘤药房Onco360现在是Karyopharm的产品XPOVIO(selinexor)的全国专业药房网络合作伙伴,XPOVIO(selinexor)是同类首创的 XPO-1 抑制剂。XPOVIO获准用于多种肿瘤学适应症,包括:(i)与Velcade(硼替佐米)和地塞米松(xVD)联合用于治疗至少一次先前治疗后的多发性骨髓瘤患者;(ii)与地塞米松联合用于严重预先治疗的多发性骨髓瘤患者;(iii)弥漫性大B细胞淋巴瘤(DLBCL)患者,包括在至少两线全身治疗后,由滤泡性淋巴瘤引起的DLBCL。

"Onco360 is excited to expand our partnership with the team at Karyopharm and become the preferred national specialty pharmacy partner for XPOVIO," said Benito Fernandez, Chief Commercial Officer.

首席商务官贝尼托·费尔南德斯表示:“Onco360很高兴扩大与Karyopharm团队的合作伙伴关系,成为XPOVIO首选的全国专业药房合作伙伴。”

Multiple myeloma is an incurable hematological malignancy involving plasma cells. Only 50 percent of patients diagnosed with multiple myeloma survive past five years following initial diagnosis. The National Cancer Institute estimates that in 2018, approximately 30,770 new patients were diagnosed with multiple myeloma in the U.S.1 Unfortunately, most multiple myeloma patients will relapse following the first complete remission and often require continuous treatment to prevent disease progression. Previously, there were no U.S. Food and Drug Administration (FDA)-approved products or regimens for patients with relapsed or refractory multiple myeloma who failed treatment with lenalidomide, pomalidomide, bortezomib, carfilzomib, and/or daratumumab.

多发性骨髓瘤是一种涉及浆细胞的无法治愈的血液学恶性肿瘤。在被诊断患有多发性骨髓瘤的患者中,只有50%在初步诊断后存活了过去五年。美国国家癌症研究所估计,2018年,美国约有30,770名新患者被诊断出患有多发性骨髓瘤1。不幸的是,大多数多发性骨髓瘤患者将在首次完全缓解后复发,通常需要持续治疗以防止疾病进展。以前,没有经美国食品药品监督管理局(FDA)批准的针对来那度胺、泊马度胺、硼替佐米、卡非佐米和/或达拉妥单抗治疗失败的复发或难治性多发性骨髓瘤患者的产品或方案。

XPOVIO is manufactured by Karyopharm Therapeutics, and has received multiple approvals from the U.S. FDA since 2019.2 XPOVIO functions by selectively binding to and inhibiting the nuclear export protein XPO-1.

XPOVIO由Karyopharm Therapeutics制造,自2019年以来已获得美国食品药品管理局的多次批准。2 XPOVIO通过选择性地结合和抑制核出口蛋白 XPO-1 发挥作用。

Please see the full Prescribing Information for XPOVIO

请查看 XPOVIO 的完整处方信息

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