Site icon pharmaceutical daily

AmerisourceBergen Selected by Karyopharm to Support XPOVIO™

New rare disease therapy supported by AmerisourceBergen’s unified offerings including specialty pharmacy dispensing, distribution services, 3PL and community oncology services

VALLEY FORGE, Pa.–(BUSINESS WIRE)–AmerisourceBergen, a global healthcare solutions leader, announced today that it has been selected by Karyopharm Therapeutics Inc. (Karyopharm) to support XPOVIO™ (selinexor). AmerisourceBergen is providing a unified commercialization approach for XPOVIO™, which was approved by the U.S. Food and Drug Administration (FDA) on July 3, 2019. XPOVIO™ is a nuclear export inhibitor indicated in combination with dexamethasone for the treatment of adult patients with relapsed or refractory multiple myeloma (RRMM) who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, at least two immunomodulatory agents, and an anti-CD38 monoclonal antibody.

In the United States, there are 32,000 new cases of multiple myeloma, a cancer of plasma cells, each year.1 There are approximately 130,000 patients living with multiple myeloma in the United States today.2 The blood cancer is characterized by disease-related symptoms, including fatigue or weakness, unusual bleeding or bruising, and bone pain or fractures.3 Patients who suffer from relapsed and refractory multiple myeloma have an average five to nine month survival rate depending on the number of prior lines of therapy.4 XPOVIO™ inhibits the function of a nuclear export protein called XPO1 and induces the accumulation of tumor suppressor proteins in the cell nucleus, leading to the selective death of cancer cells.5

“We are proud to work with Karyopharm to introduce a new treatment option to our customers for patients affected by this rare disease,” said Joe Cappello, Senior Vice President, Global Specialty & Branded Product Strategy & Access at AmerisourceBergen. “At AmerisourceBergen, we act as one unified business, offering a breadth of services and custom commercialization plans to our manufacturing partners. Through this seamless experience, we can improve product performance and increase patient access to specialized therapies like XPOVIO™.”

AmerisourceBergen’s established expertise in supporting rare disease treatments helps ensure that critical medications are safely delivered from manufacturers to patients every day. AmerisourceBergen is supporting XPOVIO™ through:

AmerisourceBergen’s unified approach is supported by world-class commercialization support services – from global clinical trial and specialty logistics to patient access and adherence. By offering assistance at all stages of the product life cycle, AmerisourceBergen enables manufacturers to stay focused on developing life-saving therapies, while also having the confidence that their developments are expertly commercialized and brought to patients in need.

About AmerisourceBergen

AmerisourceBergen provides pharmaceutical products, value-driving services and business solutions that improve access to care. Tens of thousands of healthcare providers, veterinary practices and livestock producers trust us as their partner in the pharmaceutical supply chain. Global manufacturers depend on us for services that drive commercial success for their products. Through our daily work — and powered by our 21,000 associates — we are united in our responsibility to create healthier futures. AmerisourceBergen is ranked #10 on the Fortune 500, with more than $160 billion in annual revenue. The company is headquartered in Valley Forge, Pa. and has a presence in 50+ countries. Learn more at amerisourcebergen.com.

[1] Key Statistics About Multiple Myeloma. (2019, January 9). Retrieved from https://www.cancer.org/cancer/multiple-myeloma/about/key-statistics.html.

[2] SEER Cancer Stat Facts, 2019. National Cancer Institute

[3] What Is Multiple Myeloma?. (2018, February 28). Retrieved from https://www.cancer.org/cancer/multiple-myeloma/about/what-is-multiple-myeloma.html.

[4] Risk of progression and survival in multiple myeloma relapsing after therapy with IMiDs and bortezomib: A multicenter international myeloma working group study. (2011, July 29). Retrieved from https://www.nature.com/articles/leu2011196.

[5] Karyopharm Announces FDA Extension of Review Period for Selinexor New Drug Application. (2019, March 14). Retrieved from https://investors.karyopharm.com/news-releases/news-release-details/karyopharm-announces-fda-extension-review-period-selinexor-new.

Contacts

Francesca Gunning, AmerisourceBergen

610-727-7433 – Office

215-603-9264 – Mobile

fgunning@AmerisourceBergen.com

Kelly Nguyen, Tierney Communications

215-790-4181 – Office

609-385-6701 – Mobile

knguyen@tierneyagency.com

Exit mobile version