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Shorla Pharma, Eversana tie up for T-cell Leukemia treatment
Cambridge: Shorla Pharma and EVERSANA have announced a partnership to support the launch and commercialization of Shorla's oncology portfolio.
The new partnership will initially focus on SH-111, an oncology drug designed to treat T-cell leukemia, currently pending USFDA approval.
Under the terms of the agreement, Shorla maintains ownership of SH-111 as well as all financial, legal, regulatory, and manufacturing responsibilities for the product. EVERSANA receives the exclusive right to support all commercialization activities for SH-111 in partnership with Shorla.
"With the recent opening of our Cambridge, MA office, we are excited to announce EVERSANA's commercial support to bring SH-111 to patients with T-cell leukemia. This partnership will provide us with a fully integrated commercial organization to support the launch of SH-111," said Sharon Cunningham, CEO, Shorla Pharma. "New therapies for women and children are often overlooked or in short supply. Our goal is to bring to market products that represent a new standard of treatment for these patients."
In March, Shorla filed its application for SH-111 with the FDA and looks forward to expedited review and anticipates approval to bring this much needed product to market later this year. SH-111 is designed to treat T-cell leukemia, an aggressive blood and bone marrow cancer which progresses quickly. While most leukemias present in older people, T-cell leukemia is most common among children, with the current treatment often in shortage.
"Knowing that so many young patients and families eagerly await this much-needed treatment, EVERSANA stands ready to immediately deploy our commercialization expertise and infrastructure in the United States," said Jim Lang, CEO, EVERSANA. "This partnership will support Shorla's oncology innovations with our oncology commercialization expertise to ensure a successful launch and access to long-awaited treatment for patients."
Future EVERSANA services may include patient services, health economic research, market access, commercial deployment solutions, channel management, pharmacovigilance compliance and other services as the teams require.
Read also: Zydus Cadila cancer drug Lenalidomide gets USFDA okay
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751