SHIRE RELEASES DATA AT THE WORLD FEDERATION OF HEMOPHILIA CONGRESS 2018 EVALUATING VONVENDI® [VON WILLEBRAND FACTOR (RECOMBINANT)] IN ADULTS WITH VON WILLEBRAND DISEASE DURING AND AFTER SURGERY
- Study evaluated safety, efficacy of recombinant von Willebrand factor with or without recombinant FVIII
- Findings suggest potential for more tailored treatment
- VONVENDI [von Willebrand factor (Recombinant)] is approved only in the U.S.
Zug, Switzerland - May 22, 2018 - Shire plc (LSE: SHP, NASDAQ: SHPG) the global biotech leader in rare diseases, presented clinical data evaluating the capacity of recombinant von Willebrand factor (rVWF) to replenish functional VWF and restore constitutive factor VIII (FVIII) levels when administered before, during and/or after surgery for adult patients (age 18 years or older) affected by von Willebrand disease (VWD), the most common hereditary bleeding disorder.1 The results being presented tomorrow at the World Federation of Hemophilia (WFH) Congress in Glasgow, Scotland, show the potential for rVWF to help manage bleeding risks during and post-surgery. rVWF is marketed in the United States as VONVENDI® [von Willebrand factor (Recombinant)].
"There is an unmet clinical need for those living with von Willebrand disease, as they face a heightened risk of bleeding during surgery," said Flora Peyvandi, Professor of Internal Medicine at the University of Milan and the Director of the Angelo Bianchi Bonomi Hemophilia and Thrombosis Centre, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy. "People with von Willebrand disease lack proper function or quantity of von Willebrand factor, and some also have a secondary factor VIII deficiency. In this study, recombinant von Willebrand factor was administered to replace the insufficient or dysfunctional von Willebrand factor, allowing the body to naturally replenish FVIII in most patients. These study results demonstrate clinical promise as physicians were able to tailor treatment based on each patient's individual need for one or both factor therapies."
Controlling bleeding with or without recombinant FVIII
The study was a Phase 3 prospective, open-label, multicenter trial to evaluate the efficacy and safety of rVWF with or without recombinant FVIII (rFVIII) in adults (age 18 years and older) diagnosed with severe VWD perioperatively including the effect on endogenous FVIII levels by administering rVWF with or without rFVIII in 15 adults with severe VWD undergoing elective surgical procedures.2,3
Results from the study showed that all 15 study participants had overall/intraoperative hemostatic efficacy ratings of "excellent" (as good as or better than expected) or "good" (probably as good as expected).4 Ninety percent of VONVENDI infusions were administered alone (without accompanying rFVIII therapy).2 In this and other studies, one study participant tested positive for binding antibodies to VWF.4 No binding antibodies against potential impurities such as rFurin, CHO-protein or mouse IgG developed after treatment with rVWF.4
"Shire has a long heritage in hematology and we are committed to developing innovative solutions for the patients that need them most," said Andreas Busch, Head of Research and Development and Chief Scientific Officer, Shire. "These study results demonstrate potential clinical value as we look to bring a new treatment option to those living with von Willebrand disease, working toward our vision of individualized treatment and addressing unmet needs for people with bleeding disorders."
VONVENDI was first approved in December 2015 in the U.S. where it is the first and only rVWF treatment for VWD that specifically addresses the primary deficiency or dysfunction of VWF while allowing the body to replenish FVIII. In April 2018, it was approved in the U.S. for perioperative management of bleeding in adults with VWD. A Marketing Authorization Application has been submitted to EMA (European Medicines Agency).
About von Willebrand disease (VWD)
VWD is the most common inherited bleeding disorder, affecting up to 1 percent of the global population.5 VWD is caused by a deficiency or dysfunction of VWF, one of several types of proteins in the blood that are needed to facilitate proper blood clotting.1 Due to this deficiency or dysfunction in VWF, blood is not able to clot effectively in people with VWD, which results in heavy menstrual periods, easy bruising or frequent nose bleeds.1 Bleeding caused by VWD is unpredictable and varies greatly among patients with this disease.6
VONVENDI [von Willebrand factor (Recombinant)] Important Information (U.S. only)3
VONVENDI [von Willebrand factor (recombinant)] is a recombinant von Willebrand factor indicated for use in adults (age 18 and older) diagnosed with von Willebrand disease (VWD) for:
DETAILED IMPORTANT RISK INFORMATION
Do not use VONVENDI in patients who have had life-threatening hypersensitivity reactions to VONVENDI or its components (tri-sodium citrate-dihydrate, glycine, mannitol, trehalose-dihydrate, polysorbate 80, and hamster or mouse proteins).
WARNINGS AND PRECAUTIONS
Embolism and Thrombosis
Thromboembolic reactions, including disseminated intravascular coagulation, venous thrombosis, pulmonary embolism, myocardial infarction, and stroke, can occur, particularly in patients with known risk factors for thrombosis, including low ADAMTS13 levels. Monitor for early signs and symptoms of thrombosis such as pain, swelling, discoloration, dyspnea, cough, hemoptysis, and syncope, and institute prophylaxis measures against thromboembolism based on current recommendations.
In patients requiring frequent doses of VONVENDI in combination with recombinant factor VIII, monitor plasma levels for FVIII:C activity because sustained excessive factor VIII plasma levels can increase the risk of thromboembolic events.
One out of 80 VWD subjects treated with VONVENDI in clinical trials developed proximal deep vein thrombosis in perioperative period after undergoing total hip replacement surgery.
Hypersensitivity reactions, including anaphylaxis, may occur. Symptoms can include anaphylactic shock, generalized urticaria, angioedema, chest tightness, hypotension, shock, lethargy, nausea, vomiting, paresthesia, pruritus, restlessness, wheezing and/or acute respiratory distress. Discontinue VONVENDI if hypersensitivity symptoms occur and administer appropriate emergency treatment.
Neutralizing Antibodies (Inhibitors)
Inhibitors to von Willebrand factor and/or factor VIII can occur. If the expected plasma levels of VWF activity (VWF:RCo) are not attained, perform an appropriate assay to determine if anti-VWF or anti-factor VIII inhibitors are present. Consider other therapeutic options and direct the patient to a physician with experience in the care of either VWD or hemophilia A.
In patients with high levels of inhibitors to VWF or factor VIII, VONVENDI therapy may not be effective and infusion of this protein may lead to severe hypersensitivity reactions. Since
inhibitor antibodies can occur concomitantly with anaphylactic reactions, evaluate patients experiencing an anaphylactic reaction for the presence of inhibitors.
In clinical trials, the most common adverse reactions observed in greater than or equal to 2% of subjects (n=80) were generalized pruritus, nausea and dizziness.
One subject treated with VONVENDI in perioperative setting developed deep vein thrombosis after undergoing total hip replacement surgery.
For Full Prescribing Information, visit http://www.shirecontent.com/PI/PDFs/VONVENDI_USA_ENG.pdf
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NOTES TO EDITORS
Shire is the global biotechnology leader serving patients with rare diseases and specialized conditions. We seek to push boundaries through discovering and delivering new possibilities for patient communities who often have few or no other champions. Relentlessly on the edge of what's next, we are serial innovators with a diverse pipeline offering fresh thinking and new hope. Serving patients and partnering with healthcare communities in over 100 countries, we strive to be part of the entire patient journey to enable earlier diagnosis, raise standards of care, accelerate access to treatment, and support patients. Our Rare Disease and Neuroscience divisions support our diverse portfolio of therapeutic areas, including Immunology, Hematology, Genetic Diseases, Internal Medicine, Ophthalmics, Oncology, and neuropsychiatry disorders.
Championing patients is our call to action - it brings the opportunity - and responsibility - to change people's lives.
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