Skip to page content

Serial biopharma founder seeks to transform an Alzheimer's drug into an autism therapy


Mark Tepper
Serial biopharma entrepreneur Mark Tepper.
Courtesy photo

For years, hundreds of thousands of Alzheimer’s or dementia patients like local entrepreneur Mark Tepper’s late mother have relied on a drug with a modest benefit. Tepper thinks his new company can broaden its impact. 

Boston-based Eumentis Therapeutics Inc. is developing what it hopes will be a more effective cousin to the existing Alzheimer’s drug memantine, also known by the brand name Nameda. The small startup plans to jump into a clinical trial next year, fueled in part by the $3.9 million seed financing round it closed Friday. 

Tepper, the serial entrepreneur and biopharma executive behind companies like Corbus Pharmaceuticals (Nasdaq: CRBP) and Phio Pharmaceuticals Corp. (Nasdaq: PHIO), will serve as CEO. 

Eumentis’ name comes from the Latin words for “well” and “mind.” In that vein, the company hopes to tackle a wide range of cognitive disorders, starting with autism spectrum disorder. 

Research suggests that Alzheimer’s, autism and several other disorders may be linked by a molecule called glutamate. The substance mediates cognition, emotions, sensory information and motor coordination in the brain. It must be delicately balanced or it can damage nerve cells. 

Memantine is designed to block some, but not all of glutamate receptors in the nervous system. It is one of the few treatment options available for Alzheimer’s disease but it's by no means a smash hit. Researchers have found that memantine really only works in patients with severe dementia or Alzheimer’s. Studies as an autism treatment have been mixed.

The problem, according to Tepper, comes down to where and how the drug binds to glutamate receptors. Eumentis hopes its drug, known as EM-036, will more selectively plug up the receptors responsible for nerve cell death. 

Studies conducted in mice by the scientist behind EM-036, Scripps Research Institute’s Stuart Lipton, have shown promise. Lipton is most well-known for helping to develop memantine, which was approved by the FDA in 2003.  

Eumentis will start by measuring the drug’s effect on children and adults with autism, giving them either a pill or powder that can be sprinkled on applesauce or yogurt, depending on their age. After that, the company will look into uses against schizophrenia and traumatic brain injuries. 

Pitching EM-036 as a better Alzheimer’s disease treatment is further down the line. The necessary trials would need to be large and costly, Tepper noted, and insurers are more likely to prefer a generic like memantine, which has gone off-label in recent years in spite of Allergan plc’s attempts to delay it

The regulatory pathway for autism or schizophrenia is more reasonable, Tepper assessed. “Call it low-hanging fruit or whatever you want."

There are also plans to seek out a second drug candidate to develop. That will require more money. "We don’t want to be another Corbus that has to wait for Phase 3 results with a binary outcome," he said, referencing his former firm's recent clinical trial failure.


Keep Digging



SpotlightMore

See More
See More
See More
See More

Upcoming Events More

Jun
14
TBJ

Want to stay ahead of who & what is next? Sent daily, the Beat is your definitive look at Boston’s innovation economy, offering news, analysis & more on the people, companies & ideas driving your city forward. Follow the Beat.

Sign Up