The deal, announced early on Thursday, calls for $3.4 billion up
front and milestone payments up to $1.9 billion, Novartis said.
The acquisition from Takeda, which is jettisoning the medicine to
reduce debt, adds to several big Novartis transactions over the last
year as the Basel-based company both beefs up its portfolio and
sheds non-core assets to focus on prescription drugs.
It is also the latest Japanese-European deal in the pharmaceutical
sector following British drugmaker Astrazeneca's $6.9 billion
agreement in January to work with Daiichi Sankyo on an experimental
breast cancer drug.
Expected to close after July, the transaction includes 400 Takeda
employees, which analysts from Bank Vontobel in Zurich said gives
Novartis a marketing team to sell not only Xiidra but another
prospective eye drug entrant, RTH258 for macular degeneration, now
awaiting regulatory approval.
"Despite generic competition...we think that Xiidra is sufficiently
differentiated," Vontobel analyst Stefan Schneider said. "The market
(is) big enough for it to reach blockbuster status, justifying the
price."
Xiidra, with $400 million in 2018 sales and approval in markets
including the United States, Canada and Australia, competes with
Allergan's older Restasis.
Generics maker Teva has a generic version of Restasis in Canada and
is planning a launch in the United States, as is Mylan, pending
resolution of legal disputes.
Xiidra has yet to get European regulatory approval.
"Following closing, we will explore the opportunity for the other
territories acquired," a Novartis spokesman told Reuters.
BLOCKBUSTER BOUND?
For Takeda, this is its first divestment since its leveraged
takeover of Shire in January, part of a flurry of
multibillion-dollar pharmaceutical deals as drugmakers seek to buy
other companies to combat expiring patents on their blockbuster
medicines and renew their drug pipelines.
[to top of second column] |
Japan's biggest drugmaker aims to dispose of $10 billion worth of
assets to cut debt, and also said it is selling TachoSil, a surgical
patch for bleeding control, to Johnson & Johnson's Ethicon for $400
million.
"We are working to strategically simplify and optimize our
portfolio, while also rapidly deleveraging," Takeda CEO Christophe
Weber said in a statement.
For roughly 34 million U.S. dry eye sufferers, tears fail to
adequately lubricate their eyes, and the condition can become
painful, potentially leading to eye damage, Novartis said.
Xiidra, which treats signs and symptoms of dry eye by controlling
inflammation, won U.S. regulatory approval in 2016 under Shire's
watch and was considered then its most important new medicine.
"We look forward to leveraging our well-established commercial
infrastructure to bring this medicine to more patients," said Paul
Hudson, who heads Novartis's drugs business, adding the company sees
Xiidra "well positioned for blockbuster potential" topping $1
billion annual sales.
Novartis just shed its eyecare division Alcon into a separate
publicly listed company in a $30 billion shareholder spin-off, but
only after moving Alcon's prescription eye drugs into Novartis's
main pharmaceuticals business.
Novartis shares were down 0.7 percent at 0812 GMT. Takeda shares
closed up 0.2 percent in Tokyo.
(Reporting by Takashi Umekawa in Tokyo, Silke Koltrowitz and John
Miller in Zurich, Tamara Mathias and Arundhati Sarkar in Bengaluru;
Editing by Sonali Paul and Emelia Sithole-Matarise)
[© 2019 Thomson Reuters. All rights
reserved.] Copyright 2019 Reuters. All rights reserved. This material may not be published,
broadcast, rewritten or redistributed.
Thompson Reuters is solely responsible for this content. |