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FDA WARNING AND MATTHEW PERRY’S DEATH DARKEN KETAMINE’S GLOW

By Daniel Gilbert
December 26, 2023 at 6:00 a.m. EST

A makeshift memorial for actor Matthew Perry, co-star of the 1990s television
sitcom “Friends,” on Bedford Street in Manhattan on Oct. 30. (Mike
Segar/Reuters)

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Federal health authorities are intensifying their scrutiny of the drug ketamine
for treating mental health disorders, as the mind-altering compound grows in
popularity despite the lack of regulatory approval for such use.


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The Food and Drug Administration warned in October about the risks of using
pharmacy-made ketamine at home, citing the case of one patient whose breathing
slowed to a dangerous level after taking a large dose outside of a health-care
facility. Then the autopsy of actor Matthew Perry, released Dec. 15, concluded a
high dose of ketamine led to his death in October — an event that, while rare,
drove home the dark side of the anesthetic that can also be abused
recreationally.



These knocks come as the Drug Enforcement Administration continues to craft a
rule that would set new limits on how health-care professionals can use
telemedicine to prescribe tightly regulated drugs like ketamine.

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Ketamine has been used for anesthesia in hospitals for decades and illicitly as
a club drug. In more recent years, it has shown promise as a salve for
depression when conventional antidepressants have failed.

The FDA approved a derivative of ketamine, the nasal spray Spravato, in 2019.
But the strict rules governing the use of Spravato have led many people to seek
other ways of getting the drug that are legal but not FDA-approved. Clinics have
sprung up to provide infusions, while some providers prescribe a tablet that can
be taken at home.

The rapid expansion of ketamine out of health-care settings and into patients’
homes has heightened a debate among ketamine providers who see the drug as a
critical tool for combating mental illness but disagree over how it should be
used.

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“This is a wake-up call for ketamine practitioners and the wider medical
community to put clear and unified guardrails in place guided by real-world data
and medicine,” the nonprofit American Society of Ketamine Physicians,
Psychotherapists, and Practitioners said after ketamine was implicated in
Perry’s death. The group pledged to create guidelines for using ketamine at
home.

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Many practitioners consider ketamine to be safe, with less potential for abuse
than opioids. The FDA, however, hasn’t established dosing guidelines for
ketamine when used for a psychiatric condition, and the agency flags safety
concerns that include abuse, increases in blood pressure and bladder problems.
Adding to the risk, the FDA says, is using the drug at home without a
health-care provider present.

Despite such alarms, there is considerable excitement about the prospects for
ketamine and other drugs with psychedelic properties to treat mental health
disorders. Barely two weeks after the FDA’s warning, Beckley Waves, a venture
company focused on psychedelics, bought telehealth ketamine firm Nue Life for
terms that weren’t disclosed. Nue Life had been valued at $103 million as of
2022, according to data provider PitchBook. Mindbloom, a rival firm, had an
estimated value of $230 million as of 2021, according to the service.

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Nue Life has provided at-home ketamine therapy to more than 10,000 patients
across 23 states, according to the deal announcement. Daniel Love, Beckley Waves
co-founder, said “through Nue Life, we can provide affordable access to safe and
legal ketamine therapy,” adding that the firm takes the risks seriously and is
committed to strengthening safety protocols.

This doctor prescribes ketamine to thousands online. It’s all legal.

One major divide among ketamine practitioners is over how and where patients
receive treatment. One camp insists the drug is safest and most effective when
used in the presence of a trained therapist, while others argue that allowing
patients to use it at home can provide more affordable relief from depression,
anxiety and post-traumatic stress disorder.

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Each approach has trade-offs. A trained therapist on-site can help a patient
navigate the drug’s mind-altering effects and ensure physical safety, but that
can be expensive. Signing up for a virtual service can be more accessible for
some, though it doesn’t come with the same level of support as an in-person
experience.

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Raquel Bennett, a ketamine specialist and founder of the Kriya Institute,
belongs to the former camp, seeing ketamine as a tool of self-discovery. “The
goal of ethical ketamine treatment is not to have clients be dependent on
ketamine forever,” she said, adding that if prescribers don’t help patients
learn new emotional skills, “they may be contributing to creating ketamine
addiction.”

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A spokesperson for Mindbloom said it “has helped thousands of people overcome
depression and anxiety,” and that its protocols “include extensive safeguards to
ensure that treatment is effective and safe.”

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The debate over using ketamine at home intensified during the pandemic, as
Mindbloom, Nue Life and other start-ups capitalized on a federal waiver of a
requirement that prescribers evaluate patients in person before treating them
with DEA-regulated drugs. This meant that doctors could prescribe ketamine to
patients from their computers, often treating people in multiple states.

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In March, the DEA proposed a rule to govern how health-care professionals use
telehealth to prescribe controlled substances — drugs considered to have varying
degrees of potential for abuse. For drugs in ketamine’s classification, a doctor
could prescribe a 30-day supply through a telehealth visit but a patient would
need to be evaluated in person after that for the treatment to continue.

That prompted an avalanche of pushback from patients and providers who’ve come
to rely on telehealth for controlled medications ranging from Adderall to
benzodiazepines. Many said ketamine has been lifesaving for them. The DEA
received more than 38,000 comments on its proposed telemedicine rule and a
related rule for buprenorphine.

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“We believe that is among the highest number of comments we have gotten in DEA’s
history,” Anne Milgram, the agency’s administrator, said at a listening session
in September.

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Not all of those in favor of expanded access to telehealth think that ketamine
should be a part of it. At the listening session in September, Georgia Gaveras,
chief medical officer of Talkiatry, proposed that ketamine be excluded from the
telehealth rule, pointing out that patients using Spravato have to be monitored
by a health-care professional.

“We also believe that the at-home prescribing of a substance that does have huge
promise for depression also has very significant diversion risks, and we believe
that it should be regulated further,” she said, according to an event
transcript.

Some pharmaceutical firms are betting they can improve on the generic ketamine
that is prescribed off-label today.

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Adam Kaplin witnessed the power of ketamine while overseeing clinical trials
that led to the approval of Spravato, but also saw the inconvenience and cost
that comes with the FDA-required monitoring. Events like Perry’s death, he said,
show “it is a very potentially dangerous practice to give patients access to
this at home.”

Kaplin, now chief scientific officer of Mira Pharmaceuticals, is aiming to
develop a derivative of ketamine with fewer side effects. The goal, he said, is
to create a drug that even the FDA will endorse as safe for patients to take at
home.

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