HemaQuest Pharmaceuticals Receives Orphan Drug Designations for Therapeutic to Treat Hemoglobin Disorders
Posted on: Tuesday, 4 November 2008, 09:00 CST
HemaQuest Pharmaceuticals today announced that the U.S. Food and Drug Administration (FDA) has awarded the company orphan drug designations for sickle cell anemia and beta thalassemia for HQK-1001, which is an orally administered therapeutic under clinical development for these two indications.
HemaQuest President and CEO Ronald Berenson, MD, said, "Orphan drug designations confirm the urgent medical need to develop new therapies to treat these two serious and life-threatening hemoglobin disorders. These designations by the FDA also provide us with strong incentives for our novel proprietary drug candidate, HQK-1001, which initially is being developed to treat both sickle cell anemia and beta thalassemia."
Orphan drug status provides certain tax benefits and confers market exclusivity for a minimum of seven years after drug approval by the FDA to encourage companies to develop medicines that affect less than 200,000 people in the United States. Both hemoglobin disorders, sickle cell anemia and beta thalassemia, fall into this category with a combined total of less than 80,000 patients suffering from these inherited blood diseases in the U.S.
Worldwide, sickle cell anemia and beta thalassemia afflict millions of people. Few therapeutic alternatives exist for these serious and life-threatening diseases, which are associated with significant morbidity and reduced patient survival, creating a strong and pressing need for new treatments.
HemaQuest recently completed Phase 1 clinical trials of HQK-1001 in healthy subjects and plans to begin clinical studies of this compound in both sickle cell anemia and beta thalassemia in the near future. The compound's therapeutic potential was discovered by Susan Perrine, MD, the company's chief scientific officer and vice president of clinical affairs, and her colleagues at Boston University.
ABOUT HEMAQUEST PHARMACEUTICALS
HemaQuest Pharmaceuticals (www.HemaQuest.com), which was established in late 2007, is a biopharmaceutical company focused on developing small molecule therapeutics based on its short chain fatty acid derivative (SCFAD) technologies to treat hemoglobin diseases. HemaQuest is also developing other SCFADs that could prove useful in treating other hematological disorders, such as other kinds of anemia and neutropenia. The company's investors include De Novo Ventures, a Palo Alto, Calif., life sciences venture capital partnership; Forward Ventures, a life sciences venture capital firm based in San Diego; and Lilly Ventures of Indianapolis, Ind., the venture capital arm of Eli Lilly and Company.
CONTACT: Peter Lowy Business Communication Strategies T: 617-734-9980 Email Contact
SOURCE: HemaQuest Pharmaceuticals
Source: MARKET WIRE
Related Articles
- American Heart Association Late-breaking Clinical Trial Report: Risks of Anemia Drug Outweigh Benefits in Cardiovascular Disease Patients With Diabetes and Kidney Disease
- HemaQuest Wins Orphan Drug Designations for Anemia Drug
- FDA Issues New Warning for Anemia Drugs
- Children Can Be Cured of Sickle Cell Disease and Thalassemia After Sibling Cord Blood Transplantation: Results From ViaCell and Children's Hospital & Research Center Oakland
- Analysis: New Warnings on Anemia Drugs
- Amgen Shares Cheap Amid Anemia Drug Woes
- First Stage Trials Success for Affymax Anemia Drug
- DNAPrint Pharmaceutical Completes Sterility Testing on Anemia Drug Cell Lines for Clinical Development
- Roche anemia drug CERA works as once-monthly dose
- J&J sues Amgen over anemia drug sales practices
 |
 |
User Comments (0)
RSS Feeds