NEW YORK, NY, and CLEVELAND, OH–(Marketwired – September 15, 2016) –
- Preclinical efficacy data demonstrated significant benefits leading to restoration of SGSH activity and reduction of glycosaminoglycans (GAG) throughout the central nervous system (CNS) and peripheral organs
- Early biopotency signals seen in ongoing AB0-102 Phase 1/2 clinical trial directionally consistent with data seen in pre-clinical models of the MPS IIIA disease
Abeona Therapeutics Inc. (ABEO), a clinical-stage biopharmaceutical company focused on developing products for life-threatening rare genetic diseases, announced today that preclinical data supporting clinical trials for ABO-102 (AAV-SGSH), the AAV-based single intravenous gene therapy program for MPS IIIA, (Sanfilippo Type A), were published in the June issue of Molecular Therapy Methods & Clinical Development (doi:10.1038/mtm.2016.36).
Researchers concluded that “… an intravenous injection of scAAV9-U1a-hSGSH vector, leading to restoration of SGSH activity and reduction of glycosaminoglycans (GAG) throughout the central nervous system (CNS) and somatic tissues at a dose…”. Other benefits included improved learning ability, increased survival, and improved GAG storage pathology in the CNS, leading researchers to note that: “The study suggests that there is potential for gene therapy intervention in MPS IIIA at intermediate stages of the disease, and extends the clinical relevance of our systemic scAAV9-hSGSH gene delivery approach.”
“The data support the clinical translation of ABO-102 for patients with Sanfilippo syndromes, and demonstrates AAV delivery to target tissues in the central nervous system as well as peripheral organs led to resolution of the underlying disease pathology,” stated Timothy J. Miller, Ph.D., President & CEO. “This approach is also especially encouraging for potential treatment of patients with juvenile Batten disease, where patients are often initially diagnosed as a result of changes in vision, and the data demonstrate delivery of the AAV to the eye after an intravenous injection.”
Abeona Therapeutics previously announced that ABO-102 preliminary measures of clinically relevant biomarkers in the ABO-102 Phase 1/2 clinical trial provided promising signals of potential systemic and CNS clinical benefits for patients suffering with MPS IIIA. The program has been granted Orphan Product Designation in the USA and received the Rare Pediatric Disease Designation. Abeona is currently working toward opening two additional clinical sites to test ABO-102, one in Spain and one in Australia.
“These promising data continues to reinforce our conviction that our novel portfolio of gene therapies including ABO-102 for MPS IIIA have transformational potential to treat devastating monogenic diseases,” stated Steven H. Rouhandeh, Executive Chairman. “We’re excited about collaborating with our research partners and patient communities to expand ongoing clinical trials globally, as well as to leverage our insights to accelerate additional gene therapy candidates into clinical development.”
The publication article can be accessed by clicking on the following link: (http://www.nature.com/articles/mtm201636).
About ABO-102 (AAV-SGSH): ABO-102 (AAV-SGSH) is a single treatment gene therapy strategy for patients with Sanfilippo syndrome type A (MPS IIIA), which is enrolling and treating patients in a Phase 1/2 clinical trial. MPS IIIA is a rare autosomal recessive disease that is caused by genetic mutations that result in a deficiency of SGSH enzyme activity, leading to abnormal accumulation of glycosaminoglycan (specifically, heparan sulfate, or “HS”) in the CNS and systemic tissues and organs. This accumulation of HS results in neurocognitive decline, speech loss, loss of mobility, and premature death in children.
About Abeona: Abeona Therapeutics Inc. is a clinical stage company developing gene and plasma-based therapies for life-threatening rare genetic diseases. Abeona’s lead programs are ABO-102 (AAV-SGSH) and ABO- 101 (AAV-NAGLU), adeno-associated virus (AAV) based gene therapies for Sanfilippo syndrome (MPS IIIA and IIIB), respectively. Abeona is also developing EB-101 (gene-corrected skin grafts) for recessive dystrophic epidermolysis bullosa (RDEB), ABO-201 (AAV-CLN3) gene therapy for juvenile Batten disease (JBD); and ABO-301 (AAV-FANCC) for Fanconi anemia (FA) disorder using a novel CRISPR/Cas9-based gene editing approach to gene therapy for rare blood diseases. In addition, Abeona has a plasma-based protein therapy pipeline, including SDF Alpha™ (alpha-1 protease inhibitor) for inherited COPD, using our proprietary SDF™ (Salt Diafiltration) ethanol-free process. For more information, visitwww.abeonatherapeutics.com.