Pot-based prescription drug could receive FDA approval
A British pharmaceutic firm is completing clinical trials of a drug derived directly from marijuana and hopes to receive approval to market it from the Food and Drug Administration by the end of 2013.
The drug, which contains both THC and cannabidiol, has already been approved in Canada, New Zealand, and several European countries to relieve muscle spasms associated with multiple sclerosis. In the US, however, it would be sold to relieve cancer pain.
The FDA began approving drugs based on synthetic equivalents of the active ingredients in marijuana in 1985, but this would be the first drug derived from the plant itself. This is significant because, as the Associated Press points out, “The U.S. Drug Enforcement Administration categorizes pot as a dangerous drug with no medical value, but the availability of a chemically similar prescription drug could increase pressure on the federal government to revisit its position.”
“There is a real disconnect between what the public seems to be demanding and what the states have pushed for and what the market is providing,” the president of the International Cannabinoid Research Society told the AP. “It seems to me a company with a great deal of vision would say, `If there is this demand and need, we could develop a drug that will help people and we will make a lot of money.'”
Some marijuana advocates, however, worry that government approval of marijuana-based prescription drugs could become a new argument against legalization of medical marijuana. “That’s the race against time,” Kris Hermes of Americans for Safe Access told AP, “in terms of how quickly can we put pressure on the federal government to recognize the plant has medical use versus the government coming out with the magic bullet pharmaceutical pill.”
Photo from Laurie Avocado [CC-BY-2.0 (www.creativecommons.org/licenses/by/2.0)], via Wikimedia Commons