Acceleron Announces New Data Presentations at the 2015 American Society of Hematology Annual Meeting
05 Noviembre 2015 - 8:10AM
Business Wire
– Presentations span multiple hematologic
diseases including myelodysplastic syndromes, beta-thalassemia,
multiple myeloma and myelofibrosis –
Acceleron Pharma Inc. (NASDAQ:XLRN), a clinical stage
biopharmaceutical company focused on the discovery, development and
commercialization of novel therapeutic candidates that regulate
cellular growth and repair, today announced that data in six
abstracts on the investigational protein therapeutics sotatercept,
luspatercept and ACE-1332 will be presented at the 57th American
Society of Hematology (ASH) Annual Meeting and Exposition being
held in Orlando, Florida on December 5-8, 2015.
Oral presentations
Title:
Luspatercept Treatment Leads to Long
Term Increases in Hemoglobin and Reductions in Transfusion Burden
in Patients with Low or Intermediate-1 Risk Myelodysplastic
Syndromes (MDS): Preliminary Results from the Phase 2 PACE-MDS
Extension Study (Abstract #92)
Session: 637. Myelodysplastic Syndromes – Clinical Studies: New
Therapeutic Approaches
Date:
Saturday, December 5th
Time: 12:15 pm EST (Orange County Convention Center, W331) Title:
TGFβ1 Antagonist Inhibits Fibrosis in a
Murine Model of Myelofibrosis (Abstract #605)
Session: 635. Myeloproliferative Syndromes: Basic Science II Date:
Monday, December 7th Time: 11:30 am EST (Orange County Convention
Center, W331) Title:
RAP-536 (Murine ACE-536/Luspatercept)
Inhibits Smad2/3 Signaling and Promotes Erythroid Differentiation
by Restoring GATA-1 Function in Murine β-Thalassemia (Abstract
#751)
Session: 112. Thalassemia and Globin Gene Regulation: Therapeutic
Approaches to Thalassemia and Their Mechanisms Date: Monday,
December 7th Time: 4:35 pm EST (Orange County Convention Center,
Valencia A (W415A)) Title:
Luspatercept (ACE-536) Reduces Disease
Burden, Including Anemia, Iron Overload, and Leg Ulcers, in Adults
with Beta-Thalassemia: Results from a Phase 2 Study (Abstract
#752)
Session: 112. Thalassemia and Globin Gene Regulation: Therapeutic
Approaches to Thalassemia and Their Mechanisms Date: Monday,
December 7th Time: 4:45 pm EST (Orange County Convention Center,
Valencia A (W415A))
Poster presentations
Title:
Biomarkers of Ineffective
Erythropoiesis Predict Response to Luspatercept in Patients with
Low or Intermediate-1 Risk Myelodysplastic Syndromes (MDS): Final
Results from the Phase 2 PACE-MDS Study (Abstract #2862)
Session: 637. Myelodysplastic Syndromes – Clinical Studies: Poster
II Date: Sunday, December 6th Time: 6:00 - 8:00 pm EST (Orange
County Convention Center, Hall A) Title:
Phase 1 Dose-Escalation Study of
Sotatercept (ACE-011) in Combination with Lenalidomide and
Dexamethasone in Patients with Relapsed and/or Refractory Multiple
Myeloma (Abstract #4241)
Session: 653. Myeloma: Therapy, excluding Transplantation: Poster
III Date: Monday, December 7th Time: 6:00 - 8:00 pm (EST) (Orange
County Convention Center, Hall A)
The posters and presentation slides will be available in the
“Publications” section on Acceleron’s website
(www.acceleronpharma.com).
About Luspatercept
Luspatercept is a modified activin receptor type IIB fusion
protein that acts as a ligand trap for members in the Transforming
Growth Factor-Beta (TGF-beta) superfamily involved in the late
stages of erythropoiesis (red blood cell production). Luspatercept
regulates late-stage erythrocyte (red blood cell) precursor cell
differentiation and maturation. This mechanism of action is
distinct from that of erythropoietin (EPO), which stimulates the
proliferation of early-stage erythrocyte precursor cells. Acceleron
and Celgene are jointly developing luspatercept as part of a global
collaboration. Acceleron and Celgene are initiating phase 3
clinical trials that are designed to evaluate the safety and
efficacy of luspatercept in patients with myelodysplastic syndromes
(the “MEDALIST” study) and in patients with beta-thalassemia (the
“BELIEVE” study). For more information, please visit
www.clinicaltrials.gov.
About Sotatercept
Sotatercept is an activin receptor type IIA fusion protein that
acts as a ligand trap for members in the Transforming Growth
Factor-Beta (TGF-β) superfamily involved in the late stages of
erythropoiesis (red blood cell production). Sotatercept regulates
late-stage erythrocyte (red blood cell) precursor cell
differentiation and maturation. This mechanism of action is
distinct from that of erythropoietin (EPO), which stimulates the
proliferation of early-stage erythrocyte precursor cells. Acceleron
and Celgene are jointly developing sotatercept as part of a global
collaboration. Sotatercept is currently in multiple phase 2
clinical trials. For more information, please visit
www.clinicaltrials.gov.
About Acceleron
Acceleron is a clinical stage biopharmaceutical company focused
on the discovery, development and commercialization of novel
therapeutic candidates that regulate cellular growth and repair.
The company is a leader in understanding the biology of the
Transforming Growth Factor-Beta protein superfamily, a large and
diverse group of molecules that are key regulators in the growth
and repair of tissues throughout the human body, and in targeting
these pathways to develop important new medicines. Acceleron has
built a highly productive R&D platform that has generated
innovative clinical and preclinical protein therapeutic candidates
with novel mechanisms of action. These protein therapeutic
candidates have the potential to significantly improve clinical
outcomes for patients with cancer and rare diseases.
For more information, please visit www.acceleronpharma.com.
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Acceleron Pharma Inc.Todd James, 617-649-9393Senior Director,
Corporate CommunicationsorMedia:Suda Communications LLCMaureen L.
Suda, 585-387-9248
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