A BRIEF HISTORY
MDMA was first made in 1912 by Merck and was
patented as an intermediate in a
chemical synthesis (not, as often
asserted, as an appetite suppressant). It was never used clinically and not
tested in humans until the 1950s. The
first scientific study was conducted in 1953 by the army, but the results of the study were not published until 1969.
A related drug, MDA (methylenedioxyamphetamine)
was popular with drug users in the sixties,
but MDMA did not return to the scene until after it was
synthesized and tested by Sasha Shulgin and Dave Nichols in 1978. A
group of psychotherapists decided that the empathic state produced by Ecstasy could
be useful in psychotherapy by producing a temporary state of openness that could help patients achieve insight and mutual
understanding. The thera‑ peutic benefits of MDMA were not realized, but
recreational use spread quickly
during the 1980s. This led to concerns that, combined with reports of toxicity, led to its classification by the Drug
Enforcement Administration (DEA) as
a Schedule! drug (a drug with no valid clinical use). Ecstasy moved quickly into the underground drug scene and
was popularized through its use at
underground dance parties ("raves") in the United Kingdom. From there, it migrated rapidly to the
United States. The Monitoring the
Future Study showed that the annual use of MDMA rose from 4.6 percent of high school seniors in 1996 to 11.7
percent of high school seniors in
2001. However, rising concerns about the potential risks of M DMA, active education campaigns, and decreased
availability have led to an equally rapid fall in reported Ecstasy use, which
was down to 5.7 percent of high school
seniors in 2005. Use has hovered at about the same level since then, although the increased popularity
of raves has triggered a resurgence of
interest in some communities. Some groups continue to advocate for its clinical use. Several clinical
trials are ongoing in Europe, and at
least two are underway in the United States (for post-traumatic stress disorder and anxiety during end-stage
cancer).