Press Release:
CYTOCHROMA CLOSES $45 MILLION SERIES
C FINANCING
Proceeds to Advance Clinical Development Of
Lead Drug Candidates
Markham, Ontario,
Canada — July,
30, 2008 — Cytochroma today
announced the closing of a CDN $45 million Series C financing. The
financing was led by a new investor, Mitsubishi Tanabe Pharma
Corporation (“MTPC”), and supported by a number
of existing investors including Vengrowth Advanced Life Sciences
Fund Inc., Caisse de Dépôt et Placement du Québec,
Novo A/S, Canadian Medical Discoveries Fund Inc., T2C2/Bio
2000 Limited Partnership, GrowthWorks Canadian Fund Ltd.,
BDC Capital Inc., and VentureLink Brighter Future Fund Inc.
Charles
W. Bishop, PhD, Cytochroma’s President and CEO
stated, “We are grateful for the strong support of MTPC
and our existing investors as we work to achieve our goal of
becoming an integrated specialty pharmaceutical company. This
latest funding provides Cytochroma with the financial capability
to aggressively drive the development of our clinical-stage
therapeutic pipeline.”
The new funding will be used to advance Cytochroma’s
portfolio of vitamin D-based therapeutics into mid- and late-stage
clinical trials. Cytochroma’s product candidates
target disorders related to altered vitamin D metabolism in
chronic kidney disease (“CKD”) patients, and include
CTA018 and CTAP201 for the treatment of secondary hyperparathyroidism
(“SHPT”), and CTAP101 for the treatment of vitamin
D insufficiency. These three lead products address significant
markets that are expected to grow to more than $1.4 billion
annually by 2013 in North America.
In connection with the financing,
Seiichi Kiso, PhD, MBA, General Manager, Business Development & Licensing Department
of MTPC, and Joseph Regan, GrowthWork’s Vice President,
Investments, have joined Cytochroma’s Board of Directors
bringing the number of directors to six. Elizabeth Douville,
PhD, Vice President of GeneChem Management Inc., has retired
from the Board after more than nine years of service with the
Company.
Alan Lewis, Ph.D., Chairman of Cytochroma’s Board of
Directors, commented, “I would like to thank Elizabeth
for her guidance in helping to bring Cytochroma to this important
point in its development. I am also pleased to welcome
Seiichi Kiso and Joe Regan to our Board and look forward to
benefiting from their experience and expertise, as we continue
to build a strong CKD-focused specialty pharmaceutical company.”
Dr. Kiso joined Tanabe Seiyaku Co., Ltd. in
1982, where he served in managerial positions across Product
Development, R&D Planning, and Corporate Development & Licensing. He
has been General Manager, Business Development & Licensing
Department, at MTPC since October 2007. Dr. Kiso received
his MSc from Kyoto Pharmaceutical University, an MBA from Kobe
University, and a PhD from Nagoya University School of Medicine.
Mr.
Regan joined GrowthWorks in early 2003, and brings 15 years
of life sciences venture capital and pharmaceutical industry
experience. He has been active in both company creation
and the strategic growth of portfolio companies. Mr.
Regan has an Honours BSc from the University of Guelph and
an MBA from McMaster University.
About Chronic Kidney Disease
According to the
National Kidney Foundation, more than eight million patients
in the U.S. suffer from moderate CKD (Stages 3 and 4) to severe
CKD (Stage 5). Stages 3 and 4 CKD
are characterized by progressively decreasing kidney function
as measured by glomerular filtration rate. In Stage 5,
kidney function is altogether absent and patients require regular
dialysis or kidney transplant for survival. An estimated
70-90% of CKD patients have vitamin D insufficiency, which
can lead to SHPT and resultant debilitating bone diseases. Mounting
evidence continues to link vitamin D insufficiency with progression
of CKD and death. CKD is caused most frequently by diabetes
or hypertension, both of which are consequences of a growing
obesity epidemic in countries worldwide.
About Cytochroma
Cytochroma is a clinical stage
specialty pharmaceutical company focused on developing and
commercializing proprietary products to treat and prevent the
clinical consequences of vitamin D insufficiency and SHPT associated
with CKD. The Company’s
vitamin D-based therapeutics are designed to safely and effectively
treat patients with Stage 3, 4 or 5 CKD. In addition,
Cytochroma is developing novel therapies to treat hyperphosphatemia
in these same patients.
For information
contact:
Eric J. Messner
Vice President, Commercial Operations
Tel: +1 (847) 236-7707 ext. 238 (Bannockburn, IL)
Tel: +1 (905) 479-5306 ext. 338 (Markham, ON)
eric.messner@cytochroma.com
Media Inquiries:
Robert Stanislaro (FD)
Tel: +1 (212) 850-5657
robert.stanislaro@fd.com
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