Acceleron Initiates Phase 2 Study of ACE-536 to Treat Patients with Beta-Thalass

PRESS RELEASE
Acceleron Initiates Phase 2 Study of ACE-536 to Treat Patients with Beta-Thalassemia
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Novel biologic has potential to treat rare blood disorder with substantial unmet medical need

Cambridge, Mass. – March 7, 2013 – Acceleron Pharma, Inc., a biopharmaceutical company developing protein therapeutics for cancer and orphan diseases, today announced the initiation of a phase 2 study of its novel, investigational protein therapeutic, ACE-536, to treat patients with beta-thalassemia, a genetic hematologic disorder causing chronic and life-threatening anemia and serious complications affecting the spleen, liver and heart.  Patients and healthcare providers currently have limited options for the treatment of beta-thalassemia.  This is the second ongoing Phase 2 trial for ACE-536, which is being developed by Acceleron as part of a global collaboration with Celgene Corporation (NASDAQ: CELG).

“The unmet medical need in beta-thalassemia is enormous as treatment options are limited mainly to blood transfusions and iron chelating agents,” said Professor Antonio Piga, M.D., Ph.D., Director of Pediatrics at San Luigi Gonzaga University Hospital in Torino, Italy and coordinating principal investigator of the study.  “ACE-536 could address this important unmet need and I am excited to explore the potential benefits of this innovative therapeutic in a phase 2 study.”

“We are excited to start our second phase 2 trial for ACE-536,” said Matthew Sherman, M.D., Chief Medical Officer of Acceleron.  “Both the preclinical and clinical data assembled to date and our understanding of the protein’s novel mechanism of action suggest that ACE-536 may become an important new treatment option for those suffering with beta-thalassemia or other diseases that negatively impact the body’s ability to produce a sufficient number of functional red blood cells.”

About the Phase 2 Clinical Trial

The phase 2 clinical trial is designed as an open-label study to evaluate the safety, tolerability and efficacy of ACE-536 in non-transfusion dependent patients with beta-thalassemia and is being conducted in Europe.  Efficacy measures include increases in hemoglobin and red blood cell levels and biomarkers of erythropoiesis, hemolysis, iron metabolism, and bone metabolism.   For additional information on this clinical trial, please visit clinicaltrials.gov, identifier NCT01749540.

About Beta-Thalassemia

Beta-thalassemia is an inherited disease involving mutations in the beta globin gene leading to defective hemoglobin production and serious anemia.  In beta-thalassemia patients, there is an over production of red blood cell (RBC) precursors in the bone marrow, often resulting in bone deformities, decreased bone mineral density and bone strength, and pathologic fractures, yet these abundant RBC precursors fail to properly mature into functional red blood cells.  This form of defective red blood cell formation is known as ineffective erythropoiesis.  Beyond the severe anemia, many patients also suffer from multiple organ dysfunction, largely due to excess iron deposits, known as “iron overload”, resulting from the ineffective erythropoiesis and the repeated RBC transfusions to address the anemia.  Iron overload can lead to heart failure, liver fibrosis, and diabetes, among other consequences.  Current treatment for beta-thalassemia includes regular RBC transfusions and daily iron chelation therapy, which is associated with toxicities.

About ACE-536

ACE-536 is a modified type II activin receptor fusion protein that acts as a ligand trap for members in the TGF-β superfamily involved in erythropoiesis.  ACE-536 regulates late-stage erythrocyte (red blood cell) precursor cell differentiation and maturation, distinct from erythropoietin (EPO) which stimulates the proliferation of early-stage erythrocyte precursor cells.  In diseases of ineffective erythropoiesis, such as myelodysplastic syndromes (MDS) and thalassemia, in which there is an over-production of early-stage erythrocyte precursors in the bone marrow, administration of erythropoietin does not correct the underlying cause of the anemia.  By promoting the differentiation of the precursor cells into mature RBCs, ACE-536 has the potential to treat the anemia in MDS and beta-thalassemia patients.  In a phase 1 clinical study in healthy volunteers, ACE-536 produced a dose-dependent increase in red blood cell counts and hemoglobin levels.  Acceleron and Celgene are jointly developing ACE-536.

About Acceleron

Acceleron is a privately-held biopharmaceutical company committed to discover, develop, manufacture and commercialize novel protein therapeutics for orphan diseases and cancer. Acceleron’s scientific approach takes advantage of its unique insight to discover first-in-class therapies based on the TGF-β protein superfamily. Acceleron utilizes proven biotherapeutic technologies and capitalizes on the company’s internal GMP manufacturing capability to advance its therapeutic programs rapidly and efficiently. The investors in Acceleron include Advanced Technology Ventures, Alkermes, Avalon Ventures, Bessemer Ventures, Celgene, Flagship Ventures, MPM BioEquities, OrbiMed Advisors, Polaris Ventures, QVT Financial, Sutter Hill Ventures and Venrock. For further information on Acceleron, please visit www.acceleronpharma.com.

http://www.acceleronpharma.com/2013/03/acceleron-initiates-phase-2-study-of-ace-536-to-treat-patients-with-beta-thalassemia/

Andy, does this treatment have to potential to be curative or at least have ameliorating benefits for thalasemia patients having deletions or severe mutations? 
So great to see so many avenues of treatment being explored!

Thank you very kindly,

Sharmin

Cant thank you enough Sharmin, I printed your post out and keep it in a backpack we use when we go for our daughters transfusions. Anytime we are feeling down we read it!

Dear JV,

I am glad that one of my posts was helpful to you - might it be the one about what to do during a transfusion?  

I often wished that we had the support and advice of parents of older thalassemia patients when we were given Lil A's diagnosis.  Had we known then,
what we know now - we would not have been nearly as devastated and confused.  Lil A is growing up to be a healthy, considerate, intelligent, athletic and
wonderful boy and I could not have asked for more in a son.   I hope that this encourages all parents of young thals.  Your little one when will do even better than Lil A because treatment is improving each day - and before long there will be a cure.

Please feel free to drop me a line if I can help in any way,

Sharmin

Andy,

I just realized that you have addressed this question in another post - that more information is not available at this time.
I hope that something good comes out of all of this work.

Sharmin