Biogen Idec And Swedish Orphan Biovitrum Announce First Patient Dosed In Global Registrational Trial Of Long-Acting Hemophilia B Therapy

(NASDAQ: ) and Swedish Orphan (STO: BVT) announced that the first patient was dosed in a registrational, open-label, multicenter trial designed to evaluate the safety, and efficacy of the companies’ long-acting, IX (rFIXFc) in B patients. The trial, called the B-LONG study, will determine the efficacy of rFIXFc in the prevention and treatment of bleeding in approximately 75 previously-treated patients with severe B.

B requires , often two to three times a week, causing a major burden on individuals with the disorder,” said , M.D., Principal Investigator of the B-LONG trial and Medical Director of the Indiana and . “In a Phase I/IIa study, rFIXFc showed the potential to prolong protection from bleeding in severe, previously- treated patients with B.”

rFIXFc is a fully-recombinant developed using ’s novel and proprietary Fc-. In the B-LONG trial, rFIXFc’s ability to prevent bleeding using different dosing regimens will be measured by evaluating the number of breakthrough bleeding episodes annualized over the study period. The study will also evaluate the efficacy of rFIXFc in on-demand and , and compare the of a single dose of rFIXFc with a single dose of a commercially available IX product.

“We are excited that rFIXFc is the first long-acting Factor IX therapy to enter registrational trials,” said , M.D., Ph.D., Vice President and Chief Medical Officer of ’s . “We are making important progress in our efforts to develop a treatment that can make a difference to the B community.”

“rFIXFc is an innovative therapy that offers the potential to make a positive impact in the lives of people with B,” said Peter , Ph.D., Chief Scientific Officer of Swedish Orphan . “Enrolling a patient in our first registrational trial is also a notable achievement for Swedish Orphan .”

Using the same proprietary technology as rFIXFc, and Swedish Orphan are also developing a fully-recombinant, long-acting Factor VIII (rFVIIIFc) for the treatment of A. rFVIIIFc is currently being evaluated in a Phase I/IIa, open-label, dose-escalation, multicenter study to evaluate the safety, tolerability and of rFVIIIFc in A patients. For more information on the rFIXFc and rFVIIIFc trials, please visit http://www.biogenidechemophilia.com.

About B

B is a rare, inherited disorder in which the ability of a person’s blood to clot is impaired. B occurs in about 1 in 25,000 male births annually and is caused by having substantially reduced or no factor IX protein, which is needed for normal blood clotting. People with B therefore need injections of factor IX to restore the coagulation process and prevent frequent bleeds that could otherwise lead to pain, irreversible joint damage and life-threatening hemorrhages. Prophylaxis treatment with infusions two or three times per week to maintain a sufficient circulating level of coagulation factor is being increasingly used, and long-term studies demonstrate that such regimens increase the patient’s life expectancy and greatly reduce if not eliminate progressive joint deterioration.

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creates new standards of care in therapeutic areas with high unmet medical needs. is a global leader in the discovery, development, manufacturing, and commercialization of innovative therapies. Patients in more than 90 countries benefit from ’s significant products that address diseases such as lymphoma, multiple sclerosis, and rheumatoid arthritis. For product labeling, press releases and additional information about the company, please visit http://www.biogenidec.com.

Source
Swedish Orphan

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