Acceleron Initiates Phase 2 Study of Dalantercept (ACE-041) to Treat Patients with Metastatic Renal Cell Carcinoma
One of Seven Phase 2 Studies Across Three Different Acceleron Programs Initiated in the Last Three Months
Cambridge, Mass. – February 5, 2013 - Acceleron Pharma, Inc., a biopharmaceutical company developing protein therapeutics for cancer and orphan diseases, announced the initiation of a phase 2 study of dalantercept, a novel angiogenesis inhibitor that targets the activin receptor-like kinase 1 (ALK1) pathway. The phase 2 study is a two-part, randomized study of dalantercept in combination with axitinib (Inlyta®, Pfizer), a vascular endothelial growth factor (VEGF) receptor tyrosine kinase inhibitor, to treat patients with metastatic renal cell carcinoma (RCC). Acceleron, its partners, and collaborators have now initiated seven phase 2 studies across three of Acceleron's programs – dalantercept (ACE-041), sotatercept (ACE-011), and ACE-536 – since November of 2012.
"Many patients with renal cell carcinoma respond to treatment with a VEGF inhibitor yet their disease subsequently progresses," said Michael B. Atkins, M.D., Deputy Director, Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center. "We are optimistic that combining two therapies with distinct anti-angiogenesis mechanisms, a VEGF inhibitor and dalantercept, an ALK1 signaling inhibitor, can provide a more effective and durable antitumor response in these patients."
"Angiogenesis is known to be a key factor in the development and progression of renal cell carcinoma" said Matthew Sherman, MD, Chief Medical Officer of Acceleron. "Dalantercept, in combination with a VEGF inhibitor, may inhibit angiogenesis more completely which could lead to improved outcomes in RCC patients. Acceleron is excited by the potential of dalantercept and is committed to a broad development program for this promising molecule."
The clinical trial is designed as two-part study in patients with metastatic renal cell carcinoma. Part 1 is a dose-escalation study of dalantercept in combination with axitinib to evaluate the safety and tolerability of the combination as second line treatment. Part 2 is an open-label, randomized study to determine whether treatment with dalantercept in combination with axitinib prolongs progression free survival (PFS) compared to treatment with axitinib alone. For additional information on this clinical trial, please visit clinicaltrials.gov, identifier NCT01727336.
Dalantercept (ACE-041) is an investigational protein therapeutic that inhibits angiogenesis by preventing BMP9 and BMP10, proteins in the TGF-β superfamily, from interacting with activin receptor-like kinase 1 (ALK1), a cell-surface receptor found on proliferating vascular endothelial cells. Dalantercept inhibits ALK1 signaling, which is required for the development of mature, functional vasculature. In a Phase 1 clinical study in patients with advanced-stage tumors, dalantercept was generally well-tolerated and also exhibited signs of clinical activity, including patients with objective response and prolonged stable disease. In addition to the phase 2 study in patients with metastatic RCC, dalantercept is also in phase 2 clinical trials for monotherapy treatment of patients with advanced head and neck cancer (NCT01458392), endometrial cancer (NCT01642082), and ovarian cancer (NCT01720173).
About Renal Cell Carcinoma
Renal cell carcinoma (RCC) is the most common type of kidney cancer in adults, accounting for approximately 85% of cases. RCC is the sixth most common cancer diagnosis in men and an increase in incidence has been reported worldwide. Over 200,000 new patients are diagnosed with RCC worldwide each year. Treatment for advanced stages of RCC, which represents about 20% of patients, consists of immunomodulators, vascular endothelial growth factor (VEGF) receptor inhibitors, and/or mammalian target of rapamycin (mTOR) kinase inhibitors. Despite multiple products approved to treat RCC, resistance to treatment remains a serious clinical challenge.
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.