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HemaQuest Announces $20M Series A Financing for Anemia Drug Development
| Source: HemaQuest Pharmaceuticals
NEWTON, MA--(Marketwire - November 1, 2007) - HemaQuest Pharmaceuticals, a new company
developing proprietary small molecule therapeutics to treat serious blood
disorders, today announced that it received $20 million in Series A
financing.
HemaQuest will use the funds primarily to support the clinical development
of its lead drug candidate, an orally administered agent for treating
sickle cell anemia and beta thalassemia.
Investors in the funding round include De Novo Ventures, a Palo Alto,
Calif. healthcare investment partnership; Forward Ventures, a life sciences
venture capital firm based in San Diego; and Lilly Ventures of
Indianapolis, the venture capital arm of Eli Lilly and Company.
Ronald Berenson, MD, HemaQuest's president and CEO, said, "The HemaQuest
technology platform is capable of producing the first safe,
disease-modifying drugs for treating sickle cell anemia and beta
thalassemia. These hemoglobin disorders afflict several million patients in
the U.S., Europe, and worldwide. With few treatment options today, the
therapeutic agents we are developing have the potential to make a real
difference in many patients' lives."
HemaQuest intends to submit an IND for its lead molecule before the end of
2007. In addition, the company said it plans to develop additional programs
in its pipeline, including novel treatments for anemia, neutropenia, and
other hematological disorders.
"The company brings together world-class scientists, potential breakthrough
drugs, and a proven development team, putting it in an ideal position to
make major advances in treating patients with serious blood diseases," said
Lilly Ventures' Bryan Dunnivant, who will serve as chairman of HemaQuest's
board.
HemaQuest's Chief Scientific Officer and Vice President, Clinical Affairs,
Susan Perrine, MD, said, "As a practicing physician, the lack of effective
therapies to alleviate the tremendous suffering of patients with hemoglobin
disorders is discouraging. I am excited to have the opportunity to develop
targeted therapeutics based on patented discoveries made by our co-founder,
Douglas Faller, MD, PhD, and my group at Boston University."
Co-founder George Stamatayannoupolous, MD, former president of the American
Society of Hematology and one of the world's experts on hemoglobin
disorder, added, "The therapies we are developing address the major
hemoglobin abnormalities related to sickle cell anemia and thalassemia, and
have the potential to be a significant advance in treating these diseases."
Sickle cell anemia and beta thalassemia are hemoglobin disorders, known as
hemoglobinopathies. Patients with sickle cell disease suffer from acute
painful crises, strokes, lung disease, heart damage, infections and anemia.
In beta thalassemia, severe anemia requires frequent blood transfusions,
contributing to iron overload, which damages the heart, liver and other
major organs. With few therapeutic options, death at an early age is common
to both of these hemoglobinopathies.