Reuters Health Information: Genfit to conduct large liver drug trial despite setback
Genfit to conduct large liver drug trial despite setback
Last Updated: 2015-03-26
By Bill Berkrot and Ransdell Pierson
(Reuters) - French drugmaker Genfit SA said on Thursday it
will begin a late stage trial later this year of its lead
treatment for a liver-destroying condition, saying it failed a
midstage trial in part due to its inclusion of many patients
with a mild form of the disease.
The company said had it excluded data from those patients
with the mildest form of the disease known as NASH
(non-alcoholic steatohepatitis) its drug, called GFT505, would
have been deemed effective in reversing the condition.
Company officials said Genfit would likely include only more
seriously ill patients in its planned Phase III trials which
will test 1,500 to 2,000 patients.
Due to the unexpected rate of resolution of NASH in patients
who received a placebo and the large number of test sites with
very few patients, the trial did not reach its intended goal,
the company said.
When adjusting for those factors, the results were "quite
robust for NASH," Dean Hum, the company's chief scientific
officer told Reuters in an interview.
GFT505 also demonstrated a favorable effect on metabolic
factors, lowering LDL cholesterol as well as triglycerides and
levels of blood glucose. NASH has been closely associated with
obesity and diabetes.
Heart disease remains the number one killer of NASH patients
and at least one rival experiential treatment, from Intercept
Pharmaceuticals, has caused concern because it has raised LDL
levels in trials.
"This trial confirms 505 is cardioprotective," Hum said.
"This is a clear differentiation between 505 and some other
compounds."
Shares of Intercept rose 10% after Thursday's mixed results
for the rival Genfit drug.
There are currently no approved treatments for NASH, which
affects millions of people, primarily in developed nations.
Several companies are pursuing NASH treatments, including
Gilead Sciences Inc and Conatus Pharmaceuticals, which earlier
on Thursday said its experimental drug, emricasan, was more
effective than a placebo in a mid-stage fatty liver disease
study. Its shares jumped more than 26%.
Analysts have said any effective treatment for NASH or the
complications it causes, such as fibrosis and cirrhosis, could
capture annual sales of $10 billion.
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