Octapharma's Ongoing Dedication to Improving the Lives of People with Haemophilia and Von Willebrand Disease to be Showcased at the ISTH 2021 Congress
PR90450
LACHEN, Switzerland, July 5, 2021 /PRNewswire=KYODO JBN/ --
Octapharma announced today that new clinical and scientific findings
encompassing their Haematology portfolio, including Nuwiq(R), wilate(R),
octanate(R) and octanine(R)F, will be presented at the upcoming International
Society on Thrombosis and Haemostasis (ISTH) Virtual Congress, taking place on
July 17–21, 2021.
In addition to two Supported Symposia that will discuss the comprehensive
management of patients with haemophilia A and von Willebrand disease, seven
ePosters will be presented covering a broad range of clinical research and
ongoing initiatives to support the bleeding disorder community.
"Every day, our patients inspire us with their strength and resilience in
navigating the challenges of living with a bleeding disorder. We are proud to
share our most recent findings at ISTH 2021. The breadth of positive data
across our Haematology portfolio demonstrate our ongoing efforts in addressing
the differing unmet needs of patients with haemophilia and von Willebrand
disease," commented Larisa Belyanskaya, Head of IBU Haematology at Octapharma.
The symposium on von Willebrand disease, that takes place on Monday, July 19,
chaired by Dr Fernando F. Corrales-Medina, follows one woman's treatment
journey with wilate(R) and will highlight key unmet needs of people who live
with this challenging bleeding disorder. The international faculty will present
and discuss recent data and ongoing studies on the management of heavy
menstrual bleeding, pregnancy and childbirth, as well as management of
perioperative bleeding in people with VWD.
On Tuesday, July 20, Dr Robert F. Sidonio Jr. will chair Octapharma's symposium
on haemophilia A, in which experts from around the world will present both
clinical and scientific data from global collaborations on inhibitor
management, factor VIII prophylaxis and important roles of factor VIII beyond
haemostasis, aiming to support clinicians in making informed treatment
decisions.
Attendees will have the opportunity in both symposia to meet the speakers
during live Q&A sessions, and both symposia will be available on-demand to
participants after the Congress.
Olaf Walter, Board Member at Octapharma, stated that: "At Octapharma, we strive
toward addressing the substantial challenges faced by people with bleeding
disorders and to improve the lives of these individuals and their families.
ISTH is an invaluable forum for engagement with key opinion leaders, experts,
and the wider bleeding disorder community, and for sharing our expertise and
research. Our contributions to ISTH 2021 underlie our long-standing commitment
to every member of the bleeding disorder community."
Supported Symposia
From Clinical Insights to Patient Experience: Suzanne's Journey with von
Willebrand Disease
Monday 19 July, 12:30–13:30 (EDT)
Chair: Dr Fernando F. Corrales-Medina, Division of Pediatric
Hematology-Oncology, University of Miami-Miller School of Medicine, Miami, USA
Factor in the Future: Informed Treatment Decisions for Haemostasis and Beyond
Tuesday 20 July, 12:30–13:30 (EDT)
Chair: Dr Robert F. Sidonio Jr., Hemophilia of Georgia Center for Bleeding and
Clotting Disorders, Children's Healthcare of Atlanta, Emory University,
Atlanta, USA
ePosters
PB0502: Prospective, open-label, multicentre phase II study (PeKaFIX) to
evaluate the pharmacokinetic parameters of a plasma derived factor IX
concentrate and build a pharmacokinetic Bayesian model
PB0535: Long-term prophylaxis with simoctocog alfa in children
PB0549: Immunogenicity and safety of simoctocog alfa in previously treated
patients switching to simoctocog alfa in the GENA clinical trial programme
PB0590: Efficacy of simoctocog alfa in previously untreated patients with
severe haemophilia A: Final results from the NuProtect study
PB0627: PRactical Utilisation of Octapharma FVIII Concentrates in Previously
Untreated and Minimally Treated Haemophilia A Patients Entering Routine
Clinical Treatment with Nuwiq(R), octanate(R) or wilate(R) – The Protect-NOW
Study
PB0939: Plasma-derived VWF/FVIII concentrate (wilate(R)) for haemostasis in
women with VWD during childbirth
PB0926: Don't Let Bleeding Go Unnoticed – A Global Initiative to Increase
Awareness of von Willebrand Disease
About Octapharma
Headquartered in Lachen, Switzerland, Octapharma is one of the largest human
protein manufacturers in the world, developing and producing human proteins
from human plasma and human cell lines.
Octapharma employs more than 9,000 people worldwide to support the treatment of
patients in 118 countries with products across three therapeutic areas:
Immunotherapy, Haematology, and Critical Care.
Octapharma has seven R&D sites and six state-of-the-art manufacturing
facilities in Austria, France, Germany, Mexico and Sweden, and operates more
than 160 plasma donation centres across Europe and the US.
For more information, please visit: www.octapharma.com.
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SOURCE: Octapharma
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