News
One step closer
By Lauren Hines | Bond LSC
From developing a question to discovering a potential solution and putting it into practice, the journey from research to practical application is a long one. Nevertheless, each step brings that solution one step closer to reality.
Shift
Pharmaceuticals — the brainchild of Bond LSC’s Chris Lorson — has taken another
of those steps with a new patent issued last month and meetings with the Food
and Drug Administration in October 2019.
Lorson
— a Bond LSC primary investigator, professor of veterinary pathobiology and
associate dean for research and graduate studies for the College of Veterinary
Medicine — co-founded Shift three years ago in March 2017 after Lorson’s lab
had a breakthrough in his research on the genetic disorder, Spinal Muscle Atrophy
(SMA). He worked with Mizzou’s Technology Advancement Office and
entrepreneur-in-residence Steve O’Connor to dive into this business endeavor.
“Mizzou does a great job of supporting entrepreneurial activity, and
working with Sam Bish has been astounding,” Lorson said. “He really lowers the
hurdles and helps take care of the business stuff on the MU side.”
After
developing the new technology, Lorson went to Sam Bish — the senior licensing
& business development associate in the Technology Advancement Office (TAO) within the Office of
Research — to help
protect the discovery. As a faculty member, Lorson shares the rights to his
discoveries with the university since he used its resources and funds. The
initial funding for this project came from Cure SMA, a non-profit patient
advocacy group focused upon SMA. Through licensing and patenting the
technology, Shift is allowed to commercialize it even though the
university owns it.
With
the university’s help, this product moves closer to the clinic and those with
SMA are a step closer to healing.
SMA
is a genetic disorder that develops in children missing the survival motor
neuron-one gene. The disorder is the leading genetic cause of infantile death
worldwide and causes muscle weakness, respiratory failure and premature death.
SMA
is caused by the loss of a gene called SMN1. Humans have a “back-up” copy
called SMN2. SMN2 does not make enough SMN protein to prevent disease but has
been the focus of considerable interest for drug development within the SMA
field. The compound that the Lorson lab developed targets SMN2, causing SMN2 to
be “turned up” so it makes high levels of SMN protein, like SMN1. In
pre-clinical models, a single dose can extend survival ~800%.
The
compound is an antisense oligonucleotide (ASO), which is a synthetic string of
nucleic acids that bind to a sequence of the SMN2 gene. Normally SMN2 produces
a protein that has an important region that is missing. This compound forces SMN2
to make the “normal” full-length protein which would prevent disease
development.
Highlighting
the promise of personalized health care and the impact of large-scale
interdisciplinary collaboration, this type of research is part of the
University of Missouri System’s bold NextGen Precision Health Initiative. The
NextGen Initiative unites government and industry leaders with innovators from
across the system’s four research universities in pursuit of life-changing
precision health advancements.
“The university is not in the business of selling products. That’s
just not what the university does,” Bish said. “The goal with every university
technology disclosed to TAO is to get industry to commercialize it. This is what
I call the ‘Three-way win.’”
The
company wins because they produce a commercial product. The license helps money
go to the university, and the university shares some of what they received with
the inventors.
Now,
Shift is at the commercializing stage.
“Everything before 2016 was to find the lead compound,” Lorson said.
“Everything after 2016 is to prove that it’s safe and efficacious.”
Shift still needs to further develop the technology prior to submitting
it to the FDA and starting clinical trials.
Luckily,
it’s not expected for a company to fully develop a product to the market. Big pharmaceutical
companies often partner, acquire a company or license the technology after a
start-up like Shift Pharmaceuticals does the legwork to show progress and
potential.
Bish
attributes the success to the amount of money, or non-diluting capital, Shift
has raised and how Lorson created the company.
“Dr. Lorson was very smart in the way he went about this,” Bish
said. “He realized he needed partners to get this company on its feet. Some
people will say, ‘Well that shows weakness. You didn’t know how to do it on
your own.’ To me, that shows wisdom and strength because nobody knows his
science like he knows it, but there are other people that know business and
what it takes to get successfully launch and develop a biotech company that he
may not have.”
Even though Shift has far to go to make the new technology
available to those with SMA, Lorson recognizes the work that has gotten him and
his team to this point.
“Having been in the field for 20 years, it’s exciting to see it
developed,” Lorson said. “Having known many families with SMA and getting to
see them every year for 20 years, it’s exciting to see progress being made in
addition to all the other stuff that’s being done by many other labs and
companies. I think the interactions between SMA researchers and SMA families is
one of the most exciting parts of my job. It permeates what I do every day, and
I try to instill that into the lab every chance I get.”
This research is an example of how the NextGen Precision Health Institute at Mizzou is expanding collaboration in personalized health care and the translation of interdisciplinary research for the benefit of society. Partnering together with government and industry leaders, the NextGen Institute empowers bold cross-disciplinary innovation and life-changing precision health advancement targeting individual genetic, environmental and lifestyle factors. The work of the institute is a cornerstone of the University of Missouri System’s statewide NextGen Precision Health Initiative.