Acalabrutinib Granted Breakthrough Therapy Designation by US FDA for the Treatment of Patients with Mantle
Cell Lymphoma
AstraZeneca and its hematology research and development center of excellence, Acerta Pharma, today announced that the US Food
and Drug Administration (FDA) has granted Breakthrough Therapy Designation for acalabrutinib for the treatment of patients with
mantle cell lymphoma (MCL) who have received at least one prior therapy. Acalabrutinib is an investigational, highly selective,
potent Bruton tyrosine kinase (BTK) inhibitor in development for the treatment of multiple B-cell cancers.
The Breakthrough Therapy Designation is designed to expedite the development and regulatory review of new medicines that are
intended to treat a serious condition and that have shown encouraging early clinical results, which demonstrate substantial
improvement on a clinically-significant endpoint over available therapies and when there is significant unmet medical need.
Sean Bohen, Executive Vice President, Global Medicines Development and Chief Medical Officer at AstraZeneca, said: “New
treatments are urgently needed for people with mantle cell lymphoma who relapse or do not respond to therapy. Breakthrough Therapy
Designation for acalabrutinib will help us bring this potential medicine to appropriate patients as quickly as possible.”
The FDA granted Breakthrough Therapy Designation based on the totality of clinical data from the acalabrutinib development
program, including data from the Phase II ACE-LY-004 clinical trial in patients with relapsed or refractory MCL.
Flavia Borellini, PhD, Acerta Pharma Chief Executive Officer, said: “This is an exciting regulatory milestone for our work in
hematology. Acalabrutinib is a potent, irreversible BTK inhibitor with a high degree of specificity for its target. If approved, it
could be a clinically meaningful treatment option for patients with this devastating disease.”
This is the fifth Breakthrough Therapy Designation that AstraZeneca has received from the FDA for an oncology medicine since
2014, and the first for the Company in hematology. The acalabrutinib development program includes both monotherapy and combination
therapies in a broad range of blood cancers and solid tumors.
NOTES TO EDITORS
About mantle cell lymphoma (MCL)
Mantle cell lymphoma (MCL) is an aggressive B-cell non-Hodgkin lymphoma (NHL) with poor prognosis.1,2,3,4 MCL accounts
for approximately 3% to 6% of new NHL cases in Western countries each year, with an annual incidence of 0.5 per 100,000 persons and
an estimated prevalence of 3.5/100,000.2,5 The median age at diagnosis is 68 years, with a 3:1 male
predominance.2
About acalabrutinib
Acalabrutinib is an investigational highly selective, potent, covalent inhibitor of Bruton tyrosine kinase (BTK) with minimal
off-target activity observed in pre-clinical trials.6,7,8 This potential new medicine is in development for the
treatment of multiple B-cell and other cancers. The acalabrutinib development program includes both monotherapy and combination
therapy strategies in chronic lymphocytic leukemia (CLL), MCL, Waldenström macroglobulinemia, follicular lymphoma, diffuse large
B-cell lymphoma, and multiple myeloma, as well as monotherapy and combination trials in solid tumors. In total, more than 25
acalabrutinib clinical trials with more than 2,000 patients are underway or have completed. Acalabrutinib was granted Orphan Drug
Designation by the FDA for the treatment of patients with MCL in September 2015. Acalabrutinib is a potential new medicine not
approved for any current use.
About Acerta Pharma
Acerta Pharma, a member of the AstraZeneca Group, is creating novel selective therapies intended for the treatment of cancer and
autoimmune diseases. AstraZeneca acquired a majority stake interest in Acerta Pharma, which serves as AstraZeneca’s hematology
research and development center of excellence. For more information, please visit www.acerta-pharma.com.
About AstraZeneca in Oncology
AstraZeneca has a deep-rooted heritage in Oncology and offers a quickly growing portfolio of new medicines that have the potential
to transform patients’ lives and the Company’s future. With at least six new medicines to be launched between 2014 and 2020 and a
broad pipeline of small molecules and biologics in development, we are committed to advance New Oncology as one of AstraZeneca’s
five Growth Platforms focused on lung, ovarian, breast and blood cancers. In addition to our core capabilities, we actively pursue
innovative partnerships and investments that accelerate the delivery of our strategy as illustrated by our investment in Acerta
Pharma in hematology.
By harnessing the power of four scientific platforms – Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response and
Antibody Drug Conjugates – and by championing the development of personalized combinations, AstraZeneca has the vision to redefine
cancer treatment and one day eliminate cancer as a cause of death.
About AstraZeneca
AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialization of
prescription medicines, primarily for the treatment of diseases in three main therapy areas – Oncology, Cardiovascular &
Metabolic Diseases and Respiratory. The Company also is selectively active in the areas of autoimmunity, neuroscience and
infection. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For
more information, please visit www.astrazeneca-us.com and follow us on Twitter @AstraZenecaUS.
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US- 11256 Last Updated 8/17
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