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Podcast

Podcast: Psychedelics in D.C., FDA’s Framework, and New Zealand’s MDMA Prescribers

Today, we’re launching The Psychedelic News Feed’s audio companion, available in your preferred podcast app.

Every other Monday, Psychedelic Alpha editor Josh Hardman will talk you through the preceding two weeks’ key developments across psychedelic drug development, policy, and access.

It’s certainly not a fully-fledged podcast. Rather, it’s a way to stay current and receive The Psychedelic News Feed in an audio format. 

Listen to the first episode today. (Follow the podcast in your preferred app to receive new episodes directly.)

In this episode, Psychedelic Alpha’s editor Josh Hardman runs through a very busy two-week period in the field, including:

  • Three meetings, or what I’m calling ‘Psychedelics Week’, in D.C.: FDA’s public hearing, an ibogaine-related meeting hosted by ARPA-H, and a congressional briefing
  • A commentary published by top FDA staff outlining a model for psychedelic drug development
  • New Zealand’s approval of two psychiatrists to prescribe MDMA
  • And many other headlines, including: Definium Therapeutics’ Phase 3 LSD for generalised anxiety disorder readout, more data from Compass Pathways’ psilocybin for treatment-resistant depression program, Xylo’s neuroplastogen enters the clinic, Eli Lilly’s acquisition of AtaiBeckley closes, RFK Jr. hosts Bryan Hubbard on his podcast to talk ibogaine, and Usona Institute files a trademark on ‘Arumaya’ a potential brand name for its psilocybin candidate.

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Independent data-driven reporting, analysis and commentary on the psychedelics space: from business and drug development through to policy reform and research.

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