WALTHAM, Mass.--(BUSINESS WIRE)--Bioverativ Inc. (NASDAQ: BIVV), a global biotechnology company focused on the discovery, development and commercialization of innovative therapies for hemophilia and other rare blood disorders, today announced that it has entered into a definitive agreement to acquire South San Francisco-based True North Therapeutics, a privately-held, clinical-stage rare disease biotechnology company, for an upfront payment of $400 million plus assumed cash. True North investors are also eligible to receive additional payments of up to $425 million contingent on the achievement of future development, regulatory and sales milestones.
As part of the acquisition, Bioverativ will obtain worldwide rights to True North’s lead candidate, TNT009, a first-in-class monoclonal antibody in development to treat cold agglutinin disease (CAD). CAD is a rare and chronic hemolytic condition that often leads to severe anemia, requiring numerous transfusions, and can result in life-threatening thrombotic events. There are no approved therapies for CAD, which occurs in approximately 16 people per million globally, including an estimated 5,000 people in the United States.
In May 2017, the U.S. Food and Drug Administration (FDA) granted TNT009 breakthrough therapy designation for the treatment of hemolysis in patients with primary CAD, and plans for the full clinical development program, including a registrational program, are underway. Breakthrough therapy designation was created by the FDA to expedite the development and review of medicines that target serious or life-threatening conditions and have shown preliminary evidence of potential clinical benefit.
“One of our strategic priorities is to invest thoughtfully in business development with a focus on building our pipeline in areas where we believe we can make a real difference for patients,” said John Cox, Chief Executive Officer of Bioverativ. “This acquisition of True North is aligned with those goals and with our vision to become the leading rare disease company focused on blood disorders. It strengthens our pipeline with a potential first-in-class therapy to treat CAD, a rare blood disorder with a high unmet patient need.”
“People living with CAD currently have no approved treatment options and suffer with a significant disease burden including crippling fatigue, frequent transfusions and an increased risk of life-threatening thrombotic events such as pulmonary embolism and stroke,” Mr. Cox continued. “By combining True North’s industry-leading science in complement biology with Bioverativ’s expertise in hematology and robust clinical and commercial capabilities, we believe we can bring meaningful progress to CAD patients. In addition, this transaction is consistent with our capital allocation philosophy, and we expect it to create significant value for our shareholders over the long term."
“Today’s announcement and TNT009’s breakthrough therapy designation are testaments to the innovative science underpinning our lead candidate and the strength of the True North team. We are delighted to have progressed our pipeline to this stage,” said Nancy Stagliano, PhD, Chief Executive Officer of True North. “Bioverativ is well positioned to advance the development and commercialization of TNT009 on behalf of CAD patients who are greatly in need of safe and effective treatments.”
The FDA granted TNT009 breakthrough therapy designation based on data from a Phase 1b trial, which showed that TNT009 normalized hemoglobin levels in six of six study participants with primary CAD, increasing hemoglobin by an average of 4g/dL and resolving their anemia. All participants were transfusion free while on treatment. TNT009 was generally well tolerated. As of December 21, 2016, five of six participants (83.3%) with primary CAD experienced at least one adverse event; all were mild to moderate in severity and no adverse event was assessed as related to TNT009 by the investigator.
TNT009 is designed to selectively inhibit the classical complement pathway by targeting C1s and directly impacting the central mechanism of CAD. The only therapy in development that targets C1s, TNT009 has received orphan drug designation from the FDA and the European Medicines Agency. A number of other rare, complement-mediated diseases share the basic underlying pathological mechanism involving C1s that could potentially be addressed by TNT009.
True North’s second molecule, TNT020, is a discovery-stage, follow-on monoclonal antibody that targets activated C1s with the potential for less-frequent dosing and subcutaneous administration.
The acquisition will be financed through a combination of cash on hand and debt. It is subject to customary closing conditions, including the expiration of the applicable waiting period under the Hart-Scott-Rodino Antitrust Act of 1976 in the United States, and is expected to close in mid-2017.
Conference Call and Webcast
Bioverativ will hold a brief
conference call and webcast today at 8:30 a.m. ET to discuss the
transaction. The conference call can be accessed through the Investors
section of Bioverativ’s homepage, investors.bioverativ.com,
and an audio replay will subsequently be available on the website for at
least one month.
About Cold Agglutinin Disease (CAD)
CAD is a debilitating
autoimmune hemolytic anemia in which autoantibodies target red blood
cells, leading to red blood cell destruction via complement activation
initiated by the C1 complex, causing chronic anemia, severe fatigue and
potentially fatal thrombotic events. CAD occurs in approximately 16
people per million, affecting an estimated 5,000 people in the United
States. Typically, symptom onset begins around age 60. There are
currently no approved therapies for CAD. Treatment is aimed at
normalizing hemoglobin levels through blood transfusions, steroids or
off-label immunotoxic therapy; however, current treatment options are
often intensive, incomplete or nondurable, leaving patients dependent
upon frequent transfusions, which can lead to chronic iron overload.
About TNT009
TNT009 is a first-in-class, humanized,
monoclonal antibody that is designed to selectively inhibit the
classical complement pathway by targeting C1s, a serine protease within
the C1-complex in the complement pathway of the immune system. With a
unique mechanism of action and high target specificity, TNT009 is
designed to selectively inhibit disease processes in the classical
complement pathway while maintaining activity of the alternative
complement pathway and lectin complement pathway, which are important
for immune surveillance and other functions.
About True North Therapeutics
True North Therapeutics is a
clinical stage biopharmaceutical company focused on the discovery,
development and commercialization of first-in-class product candidates
for complement-mediated diseases. The company’s lead product candidate,
TNT009, is designed to selectively inhibit a target in the classical
complement pathway. True North’s antibody drug development is focused on
the treatment of certain rare diseases mediated by the complement
system. True North Therapeutics is located in South San Francisco,
California. For more information, please visit www.truenorthrx.com.
About Bioverativ
Bioverativ is a global biotechnology
company dedicated to transforming the lives of people with hemophilia
and other rare blood disorders through world-class research, development
and commercialization of innovative therapies. Launched in 2017
following separation from Biogen Inc., Bioverativ builds upon a strong
heritage of scientific innovation and is committed to actively working
with the blood disorders community. The company’s mission is to create
progress for patients where they need it most and its hemophilia
therapies when launched represented the first major advancements in
hemophilia treatment in more than two decades. For more information,
visit www.bioverativ.com or
follow @bioverativ
on Twitter.
Safe Harbor
This press release contains forward-looking
statements, including statements relating to: the completion of the
transaction with True North and timing thereof; the expected benefits of
the transaction, including the potential to bring meaningful progress to
CAD patients and create shareholder value; and anticipated clinical
trials and the timing thereof. These forward-looking statements may be
accompanied by such words as “anticipate,” “believe,” “could,”
“estimate,” “expect,” “forecast,” “intend,” “may,” “plan,” “potential,”
“project,” “target,” “will” and other words and terms of similar
meaning. You should not place undue reliance on these statements.
These forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements, including: risks that the transaction will be completed in a timely manner or at all; risks of failure to satisfy the conditions precedent to completion of the transaction, including the ability to secure regulatory approvals in a timely manner or at all; uncertainty of whether Bioverativ can achieve the expected benefits from the transaction and successfully integrate the operations of True North; risks of unexpected costs, liabilities or delays; integration difficulties, including the ability to retain key personnel; risks that Bioverativ will be able to obtain financing on satisfactory terms, if at all; risks relating to the protection of intellectual property; risks and uncertainties relating to product development, clinical trials, regulatory process and approvals, and commercialization that may impact or alter Bioverativ’s anticipated business plans, strategies and objectives; and other risks and uncertainties described in the Risk Factors section of Bioverativ's quarterly and annual filings with the Securities and Exchange Commission.
These statements are based on our current beliefs and expectations and speak only as of the date of this press release. We do not undertake any obligation to publicly update any forward-looking statements, whether as a result of new information, future developments or otherwise.
