DAF/COMP/WD(2018)45 │
9
NON-PRICE EFFECTS OF MERGERS - NOTE BY THE UNITED STATES
Unclassified
generic product;
(3) two companies both developing generic products in an existing
market;
and (4) two companies both developing generic products in a market where
there is no generic currently available.
These pharmaceutical cases typically involved
the introduction of a generic product that offers significant price savings, but does not
result in marketplace innovation in the classic sense of developing something beyond
what exists today.
23. In other markets, a proposed transaction between an existing competitor and a
future entrant working on a product that customers would likely view as superior to
existing products have raised significant competitive concerns. In 2009, the FTC
challenged Thoratec Corporation’s proposed $282 million acquisition of rival medical
device maker HeartWare International, Inc., charging that the transaction would
substantially reduce competition in the U.S. market for left ventricular assist devices
(LVADs). LVADs are a life-sustaining treatment for patients with advanced heart
failure.
Thoratec’s HeartMart II product was the only commercial LVAD available in
the United States. Its competitor, HeartWare, was engaged in clinical trials for what
many considered to be a superior device, the HVAD. FDA approval was expected by
2012. Although the path to regulatory approval of these devices was not assured, the
Commission relied on evidence that HeartWare’s device was the most likely future
competitor to Thoratec’s HeartMate II, and other companies developing LVADs were
significantly behind in developing competitive products. The parties abandoned their
merger plans.
24. In markets with significant lead times for effective entry, an incumbent’s
acquisition of an emerging competitor may delay beneficial entry indefinitely. The
Department recently challenged Westinghouse Air Brake Technology Corporation’s
(“Wabtec”) acquisition of Faiveley. The Department alleged the transaction, as originally
structured, would have substantially lessened competition for the development,
manufacture, and sale of various freight railcar brake components. Prior to the
acquisition, acquisition-target Faiveley had formed a joint venture with another rail
equipment supplier that allowed it to bundle brake components and compete more
supplier to compete against Warner Chilcott’s branded product. Moreover, no other generic
supplier is likely to enter the market for a significant period of time. Thus, the combined firm
would likely delay the entry of Actavis’s generic version of Loestrin 24 FE or, at a minimum,
cause Actavis’s generic drug to compete less vigorously against Warner Chilcott’s branded
product, resulting in higher prices for consumers. Similarly, in the markets for Lo Loestrin FE and
Atelvia, Actavis may be the first and only generic competitor to Warner Chilcott’s branded
products for a significant period absent the Proposed Acquisition. By eliminating this potential
competition between Warner Chilcott and Actavis in each of these markets, the Proposed
Acquisition would harm U.S. consumers by substantially increasing the likelihood of higher post-
acquisition prices for Lo Loestrin FE and Atelvia.”).
See, e.g., In the Matter of Mylan, N.V., Dkt. C-4590 (July 27, 2016).
See, e.g., In the Matter of Impax Laboratories, Inc., Dkt. C-4511 (Mar. 6, 2015).
See, e.g., In the Matter of Watson Pharmaceuticals Inc. and Actavis Inc., Dkt. C-4373 (Oct. 15,
2012); In the Matter of Endo Health Solutions, Inc. and Boca Life Sciences Holdings, LLC, Dkt.
C-4430 (Jan. 30, 2014); In the Matter of Mylan Inc. and Agila Specialties Global Pte. Ltd., Dkt. C-
4413 (Sept. 26, 2013).
In the Matter of Thoratec Corp., Dkt. 9339 (July 30, 2009).