Phase 3 results announced for paediatric study of investigational therapy Eloctate(TM) for haemophilia A
Biogen Idec and Swedish Orphan Biovitrum AB (Sobi) have released positive top-line results of the Kids A-LONG Phase 3 clinical study that evaluated the safety and efficacy of Eloctate(TM), an investigational recombinant factor VIII Fc fusion protein product candidate, in children with severe haemophilia A. Eloctate was generally well-tolerated and no inhibitors (neutralising antibodies that may interfere with the activity of the therapy) were detected. Efficacy analyses showed twice-weekly prophylactic dosing with Eloctate maintained low bleeding rates in children.
Kids A-LONG is the first study to evaluate a long-lasting, investigational haemophilia therapy in children under 12 years old. Eloctate was developed using a process called Fc fusion and is designed to prolong the circulation of infused clotting factor in the body. The successful completion of this study will support applications for paediatric indications globally and is an important step to obtaining marketing authorisation in Europe. The European Medicines Agency requires the inclusion of paediatric study data in a marketing application for a new haemophilia therapy.
"Prophylactic treatment is recommended for children with severe haemophilia due to its proven health benefits. However, current prophylactic injection schedules are challenging for many children with haemophilia A and their parents," said Glenn Pierce, M.D., Ph.D., senior vice president of Hematology, Cell and Gene Therapies at Biogen Idec. "The results of this study support the potential for Eloctate to address a significant need for children with haemophilia A by providing prolonged intervals between scheduled prophylactic injections to protect against bleeding episodes."
Kids A-LONG investigated the safety, efficacy and pharmacokinetics (measurement of the presence of the drug in a person's body over time) of Eloctate in previously treated children under 12 years old with severe haemophilia A. The primary endpoint of the study was to evaluate the frequency of inhibitor (neutralising antibody) development and none were detected. Secondary endpoints included the overall and spontaneous annualised bleeding rates (ABR), or projected number of yearly bleeding episodes, and the number of injections used to prevent and treat bleeding episodes.
In the study, the relative increase in half-life in children with severe haemophilia A was consistent with the 1.5-fold increase in half-life seen in the A-LONG study of adults and adolescents. Children treated prophylactically with Eloctate had an overall median ABR of 2.0 and a median ABR for spontaneous bleeds of 0.0. Forty-six per cent of participants in the study experienced zero bleeding episodes. Overall, ninety three per cent of bleeding episodes were controlled by one to two injections of Eloctate. Additional analyses of the Kids A-LONG study are ongoing, and the companies plan to present detailed results at a future scientific meeting.
"Sobi and Biogen Idec recognise the importance of advancing treatment options for adults and children with haemophilia," said Birgitte Volck, M.D., Ph.D., senior vice president development and chief medical officer of Sobi. "The successful completion of the Kids A-LONG study in children under 12 years old is an important step to bringing this potential new treatment option to adults and children with haemophilia A and a milestone that will enable regulatory submission in Europe."
About Kids A-LONG
Kids A-LONG was a global, open-label, multi-centre Phase 3 study involving 71 boys with severe haemophilia A (factor VIII activity less than 1 IU per dL, or 1 per cent) with at least 50 prior exposure days to factor VIII therapies. The study was conducted at 23 haemophilia treatment centres in eight countries. Overall, 67 participants (94 per cent) completed the study (33 under six years old and 34 six to 11 years old). The average time participants spent in the study was 25 weeks and 61 participants received Eloctate injections on at least 50 separate days (exposure days) to assess inhibitor development.
All study participants were to be initially treated with twice-weekly prophylactic injections of Eloctate (25 IU/kg day 1, 50 IU/kg day 4). Study investigators could adjust the dose or interval based on individual response. Approximately ninety per cent of study participants were on twice-weekly dosing at the end of the study.
Eloctate was generally well-tolerated. No inhibitors to Eloctate were detected and no cases of serious allergic reactions were reported in any participants, all of whom switched from commercially available factor VIII products. No serious adverse events were assessed to be related to drug by the investigator. Two non-serious events, rash and myalgia (muscle pain), were considered related to Eloctate treatment and were reported in one participant each. No participant discontinued the study due to an adverse event after receiving Eloctate. The pattern of treatment-emergent adverse events reported was typical of the population studied and generally consistent with results seen in adolescents and adults in the A-LONG study.
Eloctate is an investigational, recombinant clotting factor therapy developed for haemophilia A by fusing factor VIII to the Fc portion of immunoglobulin G subclass 1, or IgG1 (a protein commonly found in the body). It is believed that this enables Eloctate to use a naturally occurring pathway to prolong the time therapy remains in the body. While Fc fusion has been used for more than 15 years, Biogen Idec is the only company to apply it to the treatment of haemophilia.
Regulatory applications for Eloctate approval are currently under review in several countries including the United States, Australia, Canada and Japan.
About Haemophilia A
Haemophilia A is a rare, chronic, genetic disorder in which the ability of a person's blood to clot is impaired, due to missing or reduced levels of a protein known as factor VIII. People with haemophilia A experience recurrent and extended bleeding episodes that cause pain and irreversible joint damage. Some of these bleeding episodes can be life-threatening. According to the World Federation of Hemophilia, an estimated 142,000 people worldwide are identified living with haemophilia A. Prophylactic injections of factor VIII can temporarily replace the clotting factor necessary to control bleeding and prevent new bleeding episodes.
Inhibitor development is a response of the body's immune system that interferes with the activity of therapy. About 25 to 30 per cent of people with severe haemophilia A develop inhibitors during their lifetime. Inhibitors typically develop after a median of 8-10 exposure days (EDs), though this number varies widely.