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Microbia and Forest Laboratories Announce Linaclotide Co-Development and Co-Marketing Collaboration

   Microbia Logo. (PRNewsFoto/Microbia, Inc.)

CAMBRIDGE AND NEW YORK, MA AND NY UNITED STATES
   Forest Laboratories Inc. logo. (PRNewsFoto)

NEW YORK, NY USA
    CAMBRIDGE, Mass. and NEW YORK, Sept. 17 /PRNewswire-FirstCall/ --
Microbia, Inc. and Forest Laboratories, Inc. (NYSE: FRX), today announced
that they have entered into a 50/50 partnership in the United States to
co-develop and co-market Microbia's first-in-class compound linaclotide.
Linaclotide is currently being investigated for the treatment of
constipation-predominant irritable bowel syndrome (IBS-C), chronic
constipation (CC), and other gastrointestinal disorders.
    (Logo: http://www.newscom.com/cgi-bin/prnh/20070917/NYM031LOGO )
    (Logo: http://www.newscom.com/cgi-bin/prnh/20001011/FORESTLOGO )
    Under the terms of the agreement, Forest will initially pay Microbia
$70 million in licensing fees. Microbia and Forest will jointly and equally
fund development and commercialization of linaclotide in the United States,
sharing profits equally. Additionally, Forest will have exclusive rights in
Canada and Mexico and will pay Microbia a royalty on sales in these
countries. Microbia retains all rights to the product outside of North
America. Total licensing and milestone payments to Microbia if linaclotide
is successfully developed and commercialized in the United States could
total $330 million over the term of the collaboration.
    Howard Solomon, Chairman and Chief Executive Officer of Forest, said,
"We are very pleased to have entered into this collaboration with Microbia.
Linaclotide offers the possibility of genuine relief for the millions of
patients suffering from chronic constipation and IBS-C, for which there are
currently few treatment options. Chronic constipation and IBS-C patients
are treated largely by primary care physicians, where the Forest sales
force has already built excellent relationships. We are particularly
excited to be working closely with Microbia, an innovative pharmaceutical
company with a strong and proven management and scientific team."
    Linaclotide is currently undergoing Phase 2b clinical testing in
patients with IBS-C and CC. In earlier clinical studies, linaclotide
demonstrated improved bowel function in patients with IBS-C and CC. These
studies also showed linaclotide was well tolerated with a low incidence of
adverse events. Linaclotide is an agonist of the guanylate cyclase type-C
receptor found in the intestine and acts by a mechanism distinct from
previously developed products for IBS-C and CC. Linaclotide is administered
orally but acts locally in the intestine with no measurable systemic
exposure. Microbia and Forest intend to initiate Phase 3 studies in the
second half of 2008.
    "Joining forces with Forest is the best way to maximize linaclotide's
value for patients and investors," said Peter Hecht, Microbia's Chief
Executive Officer. "Forest uniquely combines world-class primary care
commercial capabilities and an entrepreneurial and collaborative culture.
Our companies share a common vision and commitment for getting linaclotide
to IBS-C and CC sufferers."
    About Irritable Bowel Syndrome (IBS)
    One out of six adults in developed countries suffers from IBS, a
chronic condition marked by abdominal pain and disturbed bowel function.
IBS accounts for 12% of adult visits to primary care physicians and is the
most common disorder diagnosed by gastroenterologists. Health care costs
associated with IBS exceed $25 billion annually. IBS patients fall into
three subgroups- constipation-predominant (IBS-C), diarrhea-predominant
(IBS-D), and alternating (IBS-A)-and 30% to 40% of these patients suffer
from IBS-C. There are currently few available therapies to treat the nine
million U.S. patients diagnosed with IBS-C.
    About Chronic Constipation (CC)
    As many as 26 million Americans suffer from CC. Patients with CC often
experience hard and lumpy stools, straining during defecation, a sensation
of incomplete evacuation, and fewer than three bowel movements per week.
The discomfort of CC significantly affects patients' quality of life by
impairing their ability to work and participate in typical daily
activities.
    About Linaclotide
    Linaclotide is a first-in-class compound currently being tested for the
treatment of IBS-C, CC, and other gastrointestinal disorders. Linaclotide
is an agonist of guanylate cyclase type-C, a receptor found on the lining
of the intestine. In preclinical testing linaclotide was shown to increase
fluid secretion into the intestine, accelerate intestinal transit, and
decrease visceral pain. Linaclotide was designed to exert its effect on the
intestine with minimal systemic exposure. In Phase 2 trials, linaclotide
improved bowel function as measured by both complete spontaneous bowel
movements and spontaneous bowel movements in patients with CC and IBS-C.
Linaclotide is currently being tested for these indications in a pair of
Phase 2b trials, which together will enroll 700 patients. A composition of
matter patent application is pending for linaclotide, which, if issued
would provide protection to 2024, subject to extension.
    About Microbia
    Microbia (http://www.microbia.com) is an entrepreneurial pharmaceutical
company dedicated to the science and art of great drug-making. Three of the
Company's drug candidates are in clinical studies-linaclotide for the
treatment of IBS-C, CC, and other gastrointestinal disorders; and MD-0727
and MD-3124 for the treatment of hypercholesterolemia. Microbia also has a
growing pipeline of additional drug candidates. Microbia Precision
Engineering, Inc., a majority-owned subsidiary of Microbia, Inc., is an
industrial biotechnology company developing and commercializing novel
bioprocesses for the production of specialty chemicals. Microbia has raised
$231 million in private equity financing and is located in Cambridge,
Massachusetts.
    About Forest Laboratories Inc. and Its Products:
    Forest Laboratories' (http://www.frx.com) is a US-based specialty
pharmaceutical company with a growing line of products, including:
Lexapro(R) (escitalopram oxalate), a selective serotonin reuptake inhibitor
(SSRI) antidepressant indicated for the initial and maintenance treatment
of major depressive disorder and for generalized anxiety disorder in
adults; Namenda(R) (memantine HCl), an N- methyl-D-aspartate
(NMDA)-receptor antagonist indicated for the treatment of moderate to
severe Alzheimer's disease; Benicar(R)* (olmesartan medoxomil), an
angiotensin receptor blocker indicated for the treatment of hypertension;
Benicar* HCT(R) (olmesartan medoxomil hydrochlorothiazide), an angiotensin
receptor blocker and diuretic combination product indicated for the second-
line treatment of hypertension; and Campral(R)* (acamprosate calcium), a
glutamate receptor modulator, indicated for the maintenance of abstinence
from alcohol in patients with alcohol dependence who are abstinent at
treatment initiation in combination with psychosocial support.
    * Benicar is a registered trademark of Sankyo Pharma, Inc., and Campral is
      a registered trademark under license from Merck Sante s.a.s., subsidiary
      of Merck KGaA, Darmstadt, Germany.
    Except for the historical information contained herein, this release
contains "forward-looking statements" within the meaning of the Private
Securities Litigation Reform Act of 1995. Because these statements involve
a number of risks and uncertainties, actual future results may differ
materially from those expressed or implied by such forward-looking
statements. Factors that could cause or contribute to such differences
include, but are not limited to the difficulty of predicting FDA approvals,
acceptance and demand for new pharmaceutical products, challenges relating
to intellectual property protection, the impact of competitive products and
pricing, the timely development and launch of new products and the risk
factors listed from time to time in Forest Laboratories' SEC reports,
including its Annual Reports on Form 10-K for the fiscal year ended March
31, 2007 and Quarterly Reports on Form 10-Q for the period ended June 30,
2007.


SOURCE Forest Laboratories, Inc.; Microbia, Inc.




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Related links:
  • http://www.frx.com
  • http://www.microbia.com/
    Photo Notes:http://www.newscom.com/cgi-bin/prnh/20070917/NYM031LOGO
    http://www.newscom.com/cgi-bin/prnh/20001011/FORESTLOGO
    AP Archive: http://photoarchive.ap.org
    PRN Photo Desk, photodesk@prnewswire.com
    CONTACT:
    Charles E. Triano, Vice President-Investor
    Relations of Forest Laboratories, Inc., +1-212-224-6714,
    Charles.Triano@frx.com; or Susan Brady, Corporate Communications,
    Microbia, Inc., 617-621-8304, sbrady@microbia.com