A new approach to treating neuropathic pain is
making a key step forward. Neuropathic pain is among
the most difficult types of pain to alleviate and
current treatments are often ineffective.
Researchers have identified a potential non-opioid
treatment. Among the most difficult types of pain to
alleviate is neuropathic pain, pain that is usually
caused by damage to nerves in various body tissues,
including skin, muscle and joints. It can cause
patients to suffer feelings like electric shocks,
tingling, burning or stabbing. Diabetes, multiple
sclerosis, chemotherapy drugs, injuries and
amputations have all been associated with
neuropathic pain, which is often chronic, sometimes
unrelenting and affects millions of people
worldwide. Many of the available pain medications
are only moderately effective at treating this type
of pain and often come with serious side effects, as
well as risk of addiction. Scientist found it to be
an effective painkiller, and the effects were rather
long-lived. When tested it on different models,
diabetic neuropathy and chemotherapy-induced
neuropathy, for example, researcher found this compound has
an incredible beneficial effect. The new compound,
dubbed FEM-1689, does not engage opioid receptors in
the body, making it a possible alternative to
existing pain medications linked to addiction. In
addition to reducing sensitivity, the compound can
help regulate the integrated stress response (ISR),
a network of cellular signaling that helps the body
respond to injuries and diseases. When well
regulated, the ISR restores balance and promotes
healing. When it goes awry, the ISR can contribute
to diseases such as cancer, diabetes and metabolic
disorders. It's goal to make this compound into a
drug that can be used to treat chronic pain without
the dangers of opioids. Neuropathic pain is often a
debilitating condition that can affect people their
entire lives, and need a treatment that is well
tolerated and effective. This work is the
culmination of a wonderful five-year collaboration
with our colleagues at UT Austin and is a great
example of academic drug discovery pushing the field
of non-opioid pain therapeutics forward. Scientist
has the potential to take us toward clinical
development in the next few years, which is
extraordinarily exciting. |