The collective results suggest that RG3039 positively modifies motor unit pathologies and dysfunction, and that it may have therapeutic benefit for SMA.
Spinal muscular atrophy (SMA) is a devastating hereditary disease that is a leading cause of infant and early childhood mortality. Motor neurons in the spinal cord are affected, resulting in muscle weakness and in many cases breathing problems. SMA is caused by insufficient levels of the survival motor neuron (SMN) protein; depending on the level of SMN protein, patients may have mild to severe forms of SMA. There is currently no cure for the disease.
The goal of early SMA drug discovery programs has been to identify small molecules that induce the SMN gene to produce sufficient levels of protein to improve motor neuron functioning in affected patients. A promising drug candidate is RG3039, which has been shown to increase nuclear gem/Cajal body numbers in cellular assays.
Says DiDonato: "We are very happy that our research was able to assist in the pharmacological characterization of RG3039 and contribute to dose selection and exposure estimates for the first studies with RG3039 in human subjects. We are indebted to my colleague, Nancy Kuntz, MD, and co-author laboratories of Drs. Jasbir Singh and Mike Kiledjian along with Repligen and Families of Spinal Muscular Atrophy (FSMA), who initiated the development of this drug candidate. The depth of our manuscript would not have been possible without this group collaboration. Also, it is reassuring that our results of improved motor unit dysfunction in SMA mice treated with RG3039 mirror the independent findings by the laboratories of Drs. Sumner and Ko. Improved neuromuscular function is an obvious goal for SMA therapies. Thus, this drug candidate warrants further investigation. Overall, this SMA candidate drug is an exciting time as we take another step forward towards developing therapies for SMA patients."
This work was supported by funding from Families of SMA and Repligen Corporation. In addition, DiDonato was supported by the National Institutes of Health.
Families of SMA funded and directed the preclinical development of RG3039 with an investment of more than $13 million. This was the first drug discovery program ever conducted specifically for SMA. Repligen licensed RG3039 in 2009 from Families of SMA for clinical development. In January 2013, Pfizer licensed the program, marking a significant advance for the SMA community by securing the commitment of one of the world's largest pharmaceutical companies to develop potential treatments for SMA. In addition to supporting DiDonato's research, Families of SMA contributed funding to the laboratories of Charlotte Sumner, MD of Johns Hopkins University and Chien Ping Ko, PhD of the University of Southern California, who have demonstrated significant improvements in another mouse model treated with RG3039.
Christine J. DiDonato, PhD is Assistant Professor of Pediatrics at Northwestern University Feinberg School of Medicine and a member of the Human Molecular Genetics Program of Ann & Robert H. Lurie Children's Hospital of Chicago Research Center.
Full citation: Gogliotti RG, Cardona H, Singh J, Bail S, Emery C, Kuntz N, Jorgensen M, Durens M, Xia B, Barlow C, Heier C, Plasterer HL, Jacques V, Kiledjian M, Jarecki J, Rusche J, DiDonato CJ. The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models. Human Molecular Genetics, first published online June 4, 2013.
Ann & Robert H. Lurie Children's Hospital of Chicago Research Center is the research arm of Ann & Robert H. Lurie Children's Hospital of Chicago, the pediatric teaching hospital for Northwestern University Feinberg School of Medicine. The research center is also one of the interdisciplinary research centers and institutes of the Feinberg School, where principal investigators who are part of the research center are full-time faculty members.
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