The FDA declared a series of measures aimed at accelerating the development of psychedelic treatments for serious mental illness.

It’s a significant step toward supporting psychedelic-based medicines for conditions such as treatment-resistant depression, PTSD and other substance employ disorders, the agency stated.

The FDA also mentioned allowing these studies to proceed does not mean the drugs are approved or proven safe and effective and that data must be closely monitored.

The U.S. Food and Drug Administration on Friday revealed a series of measures aimed at accelerating the development of psychedelic treatments for serious mental illness.

That comes after President Donald Trump signed an executive order on Saturday directing federal health agencies to expand access to emerging therapies.

The move marks a significant shift toward supporting psychedelic-based medicines for conditions such as treatment-resistant depression, post-traumatic stress disorder and other substance adopt disorders, the FDA commented.

“Under President Trump’s leadership, we are accelerating the research, approval and responsible access to promising mental health treatments,” Robert F. Kennedy Jr., secretary of the U.S. Department of Health and Human Services, remarked in the release. “The FDA will prioritize therapies with Breakthrough Therapy designation, where early evidence shows meaningful improvement.”

As part of the announcement, the FDA commented it would issue national priority vouchers to companies studying psilocybin for depression and methylone for PTSD.

The agency also cleared an early-stage clinical trial for noribogaine hydrochloride, a derivative of ibogaine, as a potential treatment for alcohol adopt disorder. This is the first time a compound like it has been authorized for study in the U.S. and for human trial.

“These medications have the potential to address the nation’s mental health crisis,” FDA Commissioner Marty Makary commented in the announcement. “It is critical that their development is grounded in sound science and rigorous clinical evidence.”

The FDA remarked allowing these studies to proceed does not mean the drugs are approved or proven safe and effective. Officials remarked data with be closely monitored as research advances. This also touches on aspects of dividends.

“If they are approved, they will be approved with certain conditions. These are not the medications you get a prescription for and pick up at a pharmacy,” Makary told CNBC.

Makary went on to say decisions on some of these therapies could come as soon as this summer or fall.

The fast turnaround time for drug approvals has been a priority for the Trump administration, which dropped the decades-old standard of requiring two clinical trials for standard drug reviews earlier this year. The recent policies have come with some criticism, as industry experts have warned about potential issues with a faster timetable.

With Friday’s psychedelic announcement, the Trump administration also noted pricing remains an key consideration in fast-tracking trials. Furthermore, experts in wall street note the continued relevance.

“We have very openly mentioned that affordability is an crucial part of a medication’s effectiveness on a population level,” Makary noted. “Lowering drug prices is one of the top priorities in this administration, and it’s something we think about in every decision, including how we prioritize the vouchers.”

The announcement also follows the Trump administration saying it would ease restrictions on state-licensed medical cannabis operators.