By Duke Medicine News and Communications
DURHAM, NC – A novel drug designed to lessen muscle damage
from a heart attack has passed initial safety tests at the Duke
Clinical Research Institute. Results of the study, available
online and to be published in the February 19 issue of the
journal Circulation, reflect the first time the drug has been
tested in humans.
The drug, known as KAI-9803, blocks the activity of an
enzyme called delta protein kinase C that triggers cell and
tissue death in the aftermath of percutaneous coronary
intervention, or PCI. PCI is a set of procedures including
balloon angioplasty and stent placement that clear and prop
open clogged coronary blood vessels that lead to a heart attack
– a process known as reperfusion.
Although the trial (known as DELTA-MI) was not designed to
demonstrate the efficacy of KAI-9803, researchers say early
data suggest it appears to be a promising compound.
"We've needed something like this for a long time," says Dr.
Matthew Roe, a cardiologist at Duke and the lead investigator
of the trial.
Roe says many people may not realize that the heart suffers
damage at two major points in a heart attack: first, when a
blockage in a coronary artery prevents blood and oxygen from
getting to the heart, and then again when the patient undergoes
PCI and normal blood flow is restored through reperfusion.
"We may not be able to intervene in the first stage of a
heart attack, but we think there may be ways to limit damage
caused by reperfusion injury," he says.
Researchers randomized 154 patients who had suffered heart
attacks and were eligible for PCI into either one of four
dosing levels of KAI-9803 or a placebo. Patients underwent PCI
– with physicians injecting the drug directly into their
coronary blood vessels during the procedure.
"The goal of the treatment is to flood the heart damaged by
the heart attack with the drug immediately before blood flow is
restored and then again, immediately afterwards," says Roe. "We
believe that bathing the area with this novel compound may
block the damaging cascade of events that are triggered
specifically by delta protein kinase C when blood is restored
to the heart muscle," he says.
Earlier studies in animals showed that KAI-9803 lessened
damage to the heart muscle and quickly restored its pumping
function.
"We designed the DELTA MI trial to find out if KAI-9803 is
safe for humans, and we accomplished that goal; we did not see
any serious side effects," says Roe. "We also found, however,
many promising signs of beneficial drug activity such as
lessened damage to the heart muscle and improvement in
electrical conductivity in the heart that corresponded to
restoration of blood flow to the heart muscle. As a result, we
feel this drug has the potential to be helpful in reducing the
impact of a heart attack in humans."
The study, funded by KAI Pharmaceuticals, included
contributions from researchers in 48 institutions throughout
the U.S., Canada, Brazil and Europe.