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News You Might Have Missed: May 1st, 2023

The article News You Might Have Missed: May 1st, 2023 was originally published on Microdose.

Welcome to the News You Might Have Missed, a weekly roundup…

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This article was originally published by Microdose

The article News You Might Have Missed: May 1st, 2023 was originally published on Microdose.

News You Might Have Missed: July 19, 2021

Welcome to the News You Might Have Missed, a weekly roundup of psychedelic medicine news to help you catch up and stay informed. 

 

 

atai Life Sciences Presents Phase 1 Study Data on GRX-917

Earlier this year, atai Life Science company GABA Therapeutics announced Positive Final Results from Phase 1 trial of GRX-917. The company has followed-up by presenting data from its trial at the Society for Biological Psychiatry (SOBP) Annual Meeting. 

The drug is being developed with the aim to treat conditions like generalized anxiety disorder (GAD), anxious depression, social anxiety disorder (SAD), panic disorder, and postpartum depression.

 

 

Mydecine Reports Positive Preclinical Results on MYCO-006 Short-Acting MDMA Analogues

Robert Roscow, CSO of Mydecine:, “Mydecine is happy to have met our development target of developing shorter acting MDMA-like compounds and looks forward to delivering these medications in human trials in the near future. This medication family has tremendous potential to aid people in need.”

 

 

Awakn Life Sciences Reports Q4 2023 And Annual Results

Anthony Tennyson, Awakn CEO commented “Awakn made significant progress during the last fiscal year. With safety and efficacy established we are progressing our lead program, AWKN-P001, which targets Severe AUD, into phase III. The majority of the costs for this trial are being paid by the UK state, resulting in this phase III, potentially definitive trial, costing Awakn only $1.25m. 

“Additionally, we partnered with a European pharma company to assess repurposing (S)-ketamine into a licenced treatment for addiction, and we are also working with Catalent on a feasibility study of MDMA, leveraging Catalent’s proprietary Zydis® Oral Disintegrating Tablet (ODT) fast dissolve technology, to investigate the possibility of shortening MDMA therapy sessions.”

 

 

The UK Parliament Grants Debate on ‘Psilocybin Access Rights’ in the House of Commons

The Conservative Drug Policy Reform Group (CDPRG) has announced that debate on ‘Psilocybin Access Rights’ has been granted in the House of Commons in mid-May.

 

Want to catch up on more industry news? Check out a previous edition of the News You Might Have Missed

 

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