Preclinical study demonstrates promising treatment for rare bone disease

Preclinical study demonstrates promising treatment for rare bone disease
Yu Yamaguchi, M.D., Ph.D., is a professor in the Human Genetics Program at SBP. Credit: SBP

Researchers at Sanford Burnham Prebys Medical Discovery Institute (SBP) have led a preclinical study demonstrating that the drug palovarotene suppresses the formation of bony tumors (osteochondromas) in models of multiple hereditary exostoses (MHE). The research, published in the Journal of Bone and Mineral Research, is an important step toward an effective pharmacological treatment for MHE, a rare genetic condition that affects about 1 in 50,000 people worldwide.

MHE (also known as multiple osteochondromas, or MO) is an inherited genetic disorder in which multiple benign tumors covered with cartilage grow at active areas of bone growth. The condition is caused by mutations in two genes: EXT1 and EXT2. Individuals with these mutations develop painful, debilitating tumors, often repeatedly during their childhood and adolescence. Surgery and pain management are currently the only treatment options for MHE patients.

"Our study shows that palovarotene is a remarkably potent inhibitor of osteochondromas, says Yu Yamaguchi, M.D., Ph.D., professor at SBP. "In our mouse model of MHE, we were able to reduce bone tumors by more than 90 percent, which is a significant improvement over the previous drugs we have tested in the same ."

"Especially promising is that palovarotene has been tested for toxicity and side effects in humans and has been shown to be well tolerated," says Yamaguchi. "This means that time line for getting the drug to the clinic for MHE may be shortened."

Clementia Pharmaceuticals licensed palovarotene from Roche Pharmaceuticals, which previously investigated the compound as a possible treatment for and evaluated its safety in more than 800 healthy volunteers and patients. Clementia Pharmaceuticals is planning to initiate a Phase 2/3 clinical trial in 2018 for patients with MHE.

"This is first time we are seeing a clear path toward a therapy that will improve the lives of MHE patients and their families," says Sarah Ziegler, vice-president of the MHE Research Foundation. "The long awaited first clinical trial for a drug to treat MHE is now a reality. This breakthrough comes after years of working with medical professionals and scientists like Dr. Yamaguchi to achieve something we have all been desperately striving for, for many years."


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Steps toward a promising therapy for a rare bone disease

More information: Toshihiro Inubushi et al, Palovarotene inhibits osteochondroma formation in a mouse model of multiple hereditary exostoses, Journal of Bone and Mineral Research (2017). DOI: 10.1002/jbmr.3341
Citation: Preclinical study demonstrates promising treatment for rare bone disease (2017, November 20) retrieved 20 June 2019 from https://medicalxpress.com/news/2017-11-preclinical-treatment-rare-bone-disease.html
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