Contact:
Pamela McDonnell
Office of Public Affairs
NYU School of Medicine
Tel: 212-404-3555
E-mail: Pamela.McDonnell@med.nyu.edu
Epilepsy Drug Can Stop Cocaine Use In Addicts
Embargoed for release at 12:00 p.m. ET on Monday, September 22, 2003
An epilepsy drug used in Europe and elsewhere can stop cocaine use
in hard-core addicts, in part by eliminating their craving for cocaine,
according to the first study to assess the treatment's effects on addicts.
The study was led by Jonathan Brodie, M.D., Ph.D., the Marvin Stern
Professor of Psychiatry at NYU School of Medicine, along with colleagues
Stephen L. Dewey, Ph.D., of Brookhaven National Laboratory, and Emilia
Figueroa, M.D., who directs several addiction treatment clinics in Mexico.
It is published in the September 22 online edition of the journal Synapse.
The addicts in the study took GVG, which stands for gamma-vinyl-GABA.
It is also known as vigabatrin and by the trade name Sabril. The drug
has been used in Europe and many other countries to treat infantile
spasms and epilepsy, but it is not approved by the Food and Drug Administration
for use in the United States.
"Our results, in which 40 percent of hard-core addicts were able
to stay clean for more than 60 days, were more spectacular than we would
have ever dreamed," says Dr. Brodie. "These addicts were able
to stay clean even without leaving the environment that had fostered
their addiction. They gained weight, they got jobs, and they are now
living with their families."
"For the first time it seems that we might have a way to treat
people suffering from the life-threatening consequences of cocaine addiction,"
says Dr. Figueroa.
"Our results suggest that this drug, in combination with psychosocial
therapy, offers a potential treatment for cocaine addiction," says
Dr. Dewey. "We now need to confirm and extend these results in
a large double-blind, placebo-controlled trial."
Financial support for this study was provided by the Biological Psychiatry
Fund of NYU School of Medicine, and partly by the U.S. Department of
Energy and the National Institute on Drug Abuse.
Over the past decade Drs. Dewey and Brodie and their colleagues have
studied GVG in animals, and have published numerous articles showing
that the treatment in animals blocks the rise in dopamine levels produced
by cocaine, nicotine and many other addicting substances. Dopamine is
a brain chemical associated with the pleasurable effects of addicting
drugs.
The animal studies drew the interest of Dr. Figueroa, who treats addicts
at the Clinica Integral de Tratamiento Contra Las Adicciones in Mexicali.
She first contacted Dr. Dewey and then Dr. Brodie last year and told
them that she wanted to test the treatment in cocaine addicts. Her pleas
were persuasive. "She was really insistent. She told me many times
that she felt completely helpless because there was nothing she could
do for the cocaine addicts who came to her clinic," says Dr. Dewey.
Finally, Drs. Brodie and Dewey designed a clinical trial protocol
that was approved by the state of Baja California and the Mexican federal
government. This study was entirely investigator initiated and conducted
without assistance from any pharmaceutical company. The researchers
purchased GVG from local pharmacies. GVG is available in Mexico as an
epilepsy treatment.
Twenty addicts, 19 men and one woman, who had been using cocaine daily
for three to 15 years, were enrolled. All of the addicts had expressed
a desire to kick their habit. Under the trial's guidelines, they had
to provide urine samples twice a week and answer daily questionnaires
about their drug use and cravings. Their urine was screened for several
drugs, including cocaine, heroin, methamphetamine, and tetrayhdrocannabinol,
the active ingredient in marijuana. In addition, the addicts received
psychosocial counseling at the clinic.
In the first week of the trial, subjects received escalating doses
of GVG up to a maximum of 3 grams daily. They were then put on a daily
maintenance dose of 4 grams. In order to complete the trial, they had
to remain free of cocaine for 28 consecutive days. After this four-week
cocaine-free period, they were tapered by one gram per day per week
for each of the following three weeks before they ended their treatment.
In the first 10 days of the trial, eight subjects dropped out because
they didn't want to stop using cocaine. Among the 12 remaining subjects,
eight (or 40 percent of the total enrolled) completed the trial and
were tapered off GVG. At the time of the study's online publication,
all eight of the subjects remain free of cocaine more than four weeks
after their GVG treatment ended. Moreover, the people who quit using
cocaine reported that their craving did not return once they tapered
off GVG.
Four of the 12 subjects who remained in the study more than ten days
were never able to stop using cocaine during the trial, even though
they also took GVG. However, three of these people were able to reduce
the amount of cocaine they took substantially, by 50 to 80 percent,
according to the study.
None of the subjects in the study reported disturbances in their vision,
a known potential side effect of GVG. The only major side effects were
daytime sleepiness and headaches that occasionally persisted for several
weeks but were never serious enough for affected subjects to request
leaving the trial. In addition, all of the people who stopped using
cocaine gained weight.
|