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Don’t miss our top 5 cancer-related stories this month,
including a guest commentary from an industry leader, our two-part series on
trends in cancer research and more!
Revolutionizing and
personalizing global health
By E. Kevin Hrusovsky, PerkinElmer Inc. As the complexity and volume of data continue to rise, bioinformatics is emerging as one of the cornerstones of personalized medicine, from enabling discovery and development of novel treatments and diagnostics to facilitating collection, analysis and interpretation of data that ultimately helps an individual patient. SPECIAL REPORT PART 1: ‘Good enough’ is no longer good enough By Randall Willis, ddn Features Editor Aiming beyond the standard of care in oncology SPECIAL REPORT PART 2:
An aside on side effects
By Randall Willis, ddn Features Editor Are we really making things better for cancer patients? High-profile oncology partnership By Jim Cirigliano, ddn Contributing Editor Araxes Pharma and Janssen Biotech ink oncology drug development deal Natural neighbors By Kelsey Kaustinen, ddn Features Editor OSU, Biosortia link up to identify natural products for potential cancer treatments |
Homing in on hematology
March 2012
SHARING OPTIONS:
SUMMIT, N.J.—Celgene Corp. started 2012 off with an eye
toward protein silencing therapeutics, snatching up privately held Avila
Therapeutics Inc. in a definitive merger agreement.
Per the terms of the agreement, Celgene will acquire Avila
for $350 million in cash, with the potential for as much as $195 million more
in milestones based on the development and regulatory of AVL-292, Avila’s most
advanced product candidate, as well as up to $380 million in potential
milestone payments based on the development and regulatory approval of
candidates generated from the Avilomics platform. The transaction has been
approved by the board of directors of both Celgene and Avila, and is expected
to close during the first quarter of 2012.
“Avila Therapeutics is a remarkable company that is aligned
with our commitment to improve the lives of patients worldwide through
innovative science and disease-altering therapies,” Dr. Tom Daniel, president
of research and early development at Celgene, said in a press release. “In
particular, we see Avila’s unique approach to protein silencing as an area of
great promise for our research initiatives in hematology, oncology and
immune-inflammatory diseases.”
Avila specializes in targeted covalent drugs, and in
addition to sharing cancer as a therapeutic area of focus with Celgene, Avila
also focuses on viral infection and autoimmune diseases. The company’s pipeline
is based on its proprietary Avilomics platform. Targeted covalent drugs are
small-molecule medicines that can silence disease-causing proteins. The drugs
form durable bonds with the targeted proteins, shutting down activity
throughout the life of the protein. As a result, targeted covalent drugs offer
selectivity and efficacy against mutations, and also represent the possibility
of a decrease in side effects. On its website, Avila notes that there are
currently more than 38 covalent drugs that have gained U.S. Food and Drug
Administration approval in the fields of oncology, inflammatory, central
nervous system, anti-infectives and vascular and gastrointestinal disorders.
AVL-292, a highly selective Bruton’s tyrosine kinase (Btk)
inhibitor and Avila’s lead candidate, is currently in Phase I clinical testing
as a treatment for lymphoma and autoimmune diseases. Btk plays a significant
role in the development and activation of B cells, and inhibition of Btk
represents a promising approach for treating B-cell driven diseases, including
hematologic cancers such as B-cell chronic lymphocytic leukemia and
non-Hodgkin’s lymphoma, and autoimmune diseases such as rheumatoid arthritis.
The drug candidate bonds to Btk to silence its activity, and preclinical
studies proved AVL-292 to be effective in animal disease models. In addition,
Avila has also developed a companion covalent probe technology that is capable
of determining how much of the target protein was bonded by the drug.
The acquisition is a good fit for Celgene in terms of focus
compatibility. As Celgene already has experience in the field of hematologic
cancers, including seven hematology compounds in various stages of clinical
development in its pipeline, the acquisition of Avila supplements its foothold
within that therapeutic area. In addition, Avila’s approach expands upon
Celgene’s own current drug discovery methods, as Celgene works on therapies
that operate through gene and protein regulation.
“Celgene and Avila are uniquely matched, both strategically
and scientifically,” Katrine Bosley, Avila’s CEO, said in a press release.
“Celgene’s global leadership in hematology and emerging franchise in
immune-inflammatory diseases will accelerate and expand the clinical
development of our Btk inhibitor program. Equally important, we value the high
standards of creativity and rigor of Celgene’s scientists. We believe working
together may accelerate the advancement of more innovative medicines from the
Avilomics platform.”
The transaction is subject to customary closing conditions,
including the expiration of the waiting period under the Hart-Scott-Rodino
Antitrust act. Celgene expects that the acquisition will be neutral to 2012
non-GAAP diluted earnings guidance.
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