In the news ... 2008
Pain patch for neuropathy fails in study
by Alan McCord
March 18, 2008
The San Mateo-based pharmaceutical company, NeurogesX, reported
in a press release February 27, 2008 early results from their recent
study of their experimental pain patch NGX-4010 to treat HIV-related
neuropathy. The results from their second Phase 3 study showed
that NGX-4010 failed to perform better than placebo.
Given the current lack of treatments for neuropathy, failure of
this skin patch to control pain caused by distal sensory polyneuropathy (DSP)
is a disappointment to people with HIV looking for a new option
for relieving their foot and hand pain. These results differ from
two earlier studies that suggested NGX-4010 did reduce pain.
The patch is placed on the skin of the affected area with pain
where the experimental drug gets absorbed into the skin with little
absorption into the bloodstream. The patch contains capsaicin,
the compound that makes chili peppers “spicy”. Earlier
studies have shown capsaicin patches control pain in some patients
with certain forms of neuropathy. In this study, NGX-4010 seemed
to be well tolerated with few side effects.
The C119 study compared 494 people, some who used the NGX-4010
skin patch to those who used placebo. Two applications were studied
in both groups: one for 30 minutes and one for 60 minutes. Participants
were followed from 2–12 weeks. Overall, those who took the
NGX-4010 patch reached a 29.5% reduction in pain while the placebo
groups reached a 24.6% reduction. Although the 60-minute application
showed better control of pain, neither application showed any clinical
difference between NGX-4010 and placebo.
In spite of these results, the company is still moving forward
with their application to the Food and Drug Administration (FDA)
to use the drug in treating post-herpetic neuralgia (PHN)
and perhaps other forms of neuropathy Early acceptance in Europe
has already occurred.
The company explained that NGX-4010 performed similarly in this
study as in others, despite the results in the placebo groups.
They hope that further analysis of data from the several studies
of 1,600 volunteers will favor the drug as a broader treatment
for neuropathy and not just PHN. However, the data from this study
suggest that NGX-4010 does not show benefit over using placebo
for HIV-associated peripheral neuropathy.
What these results means
for people with HIV is unclear. An earlier study of NGX-4010 in
HIV-positive people with neuropathy actually showed improvement
in pain. More study may be needed before the FDA considers approving
this experimental drug for the conditions the company hopes will
be covered.
For more information on peripheral neuropathy, read Project Inform's
publication, Peripheral Neuropathy.