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45 Reps Sign Letter Urging Research Cultivation License
ASA lobbying was part of a successful, many-month effort by medical marijuana
activists to get Congress to support research into cannabis therapeutics. On September
19, a letter signed by 45 members of the U.S. House of Representatives was delivered
to the U.S. Drug Enforcement Administration (DEA), urging the DEA to allow a UMass-Amherst
professor to grow marijuana for approved research studies.
Over the past four months, ASA National Office staff, led by Governmental Affairs
Director Caren Woodson, have been part of a campaign to get members of the House
to sign the bi-partisan letter to DEA Adminstrator Karen Tandy. ASA members across
the country contributed to a national grassroots campaign, contacting their representatives
to ask them to sign on.
The letter, which was authored by U.S. Representatives John Olver (D-MA) and Dana
Rohrabacher (R-CA), asks Tandy to accept DEA Administrative Law Judge Mary Ellen
Bittner's February 2007 Opinion and Recommended Ruling in support of the UMass-Amherst
Medical Marijuana Research Production Facility. The law judge's ruling is non-binding
and DEA has no deadline to decide whether to accept or reject it. The ruling is
the result of legal action sponsored by the Multidisciplinary Association for
Psychedelic Studies and supported by the American Civil Liberties Union and other
drug policy reform groups.
The DEA's handling of the UMass application to cultivate marijuana for research
studies has already elicited congressional questioning. A DEA deputy administrator
faced criticism on the subject during hearings this summer.
"The DEA is ignoring the vast scientific evidence that clearly shows medicinal
use of marijuana benefits patients who are extremely ill," said Rep. Jerrold
Nadler (D-NY), who sits on one of the committees charged with oversight. "When
it comes to providing the best treatment options to sick Americans, we should
trust doctors and medical researchers and not federal bureaucrats."
Lyle Craker, who is the director of the Medicinal Plant Program in the Department
of Plant, Insect and Soil Sciences at University of Massachusetts, Amherst, submitted
his initial application to DEA in June 2001. Craker plans to cultivate marijuana
that would be used in clinical trials to determine whether marijuana meets FDA
standards for medical safety and efficacy.
Since 1968, the federal National Institute on Drug Abuse has maintained a monopoly
on the supply of research marijuana. Judge Bittner found that NIDA has repeatedly
refused to supply marijuana for FDA-approved studies that could develop marijuana
as a prescription medicine. Federal law requires adequate competition in the production
of such Schedule I drugs as marijuana, to ensure a supply for approved research. |