"We are excited to announce the start of this important study," says
ITP is an autoimmune disorder that occurs when the body attacks its own platelets and destroys them too quickly. In children with ITP, the body is producing platelets normally but destroying them too quickly, with platelets surviving only a few hours instead of the normal seven to 10 days. The result is a low platelet count in the blood and symptoms such as petechiae, easy bruising, and bleeding events. Spontaneous remission is common in the pediatric population, however 10-20 per cent of children will develop chronic ITP1.
Symptoms in children with ITP vary but sporadic and unpredictable bleedings along with low platelet counts can lead to anxiety among both the childen and parents. In children with more severe ITP, school attendance and participation in athletic activities have been shown to decrease. Treatment decisions for patients, families and clinicians are challenging given the administration requirements and associated toxicities of the available treatments and an important unmet medical need for new treatment options still remains2.
About AVA-PED-301 Study
AVA-PED-301 is a phase 3 study evaluating the efficacy, safety, and pharmacokinetics of avatrombopag in the treatment of pediatric subjects with ITP. Eligible pediatric subjects with platelet counts <30×109/L will enter a 12-week double-blind phase followed by an open-label extension phase up to 2 years in duration. This study will enroll a total of 72 pediatric subjects (aged ≥1 to <18 years of age) in 9 countries. Subjects will be randomized to blinded therapy of either avatrombopag or placebo in a 3:1 ratio. Enrollment into the study will be staggered by descending age cohort, with a safety and pharmacokinetic review conducted before opening the next cohort for enrolment.
About Doptelet® (avatrombopag)
Doptelet is an orally administered thrombopoietin receptor agonist (TPO-RA) that mimics the biologic effects of TPO in stimulating the development and maturation of megakaryocytes, resulting in increased platelet count. It is approved by both the
About immune thrombocytopenia (ITP) in children
Immune thrombocytopenia is an autoimmune disorder characterised by low numbers of platelets, leading to bruising and an increased risk of bleeding. The incidence of primary ITP in children is 2 to 6 per 100 000 children per year3. The disorder is considered chronic when symptoms last more than 12 months. These patients have usually relapsed after various treatments and generally require treatment to reduce the risk of clinically significant bleeding.
About Sobi™
Sobi is a specialised international biopharmaceutical company transforming the lives of people with rare diseases. Sobi is providing sustainable access to innovative therapies in the areas of haematology, immunology and specialty indications. Today, Sobi employs approximately 1,500 people across
For more information, please contact
Paula Treutiger, Head of Communication & Investor Relations
+46 733 666 599
paula.treutiger@sobi.com
+46 767 248 830
maria.kruse@sobi.com
1. Terrell DR, Beebe LA, Vesely SK, Neas BR,
2.
3. Lambert et al. Blood 2017
Postal address SE-112 76
Phone: 46 8 697 20 00 www.sobi.com
https://news.cision.com/swedish-orphan-biovitrum-ab/r/first-patient-dosed-in-phase-3-study-with-avatrombopag-for-treatment-of-itp-in-children,c3305097
https://mb.cision.com/Main/14266/3305097/1385833.pdf
(c) 2021 Cision. All rights reserved., source