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Diamond Therapeutics wins ARPA-H funding for psilocybin anxiety trial

May 11, 2026
Diamond Therapeutics wins ARPA-H funding for psilocybin anxiety trial

By AI, Created 11:11 AM UTC, May 20, 2026, /AGP/ – Diamond Therapeutics received a multi-million dollar ARPA-H award to expand its phase 2 generalized anxiety disorder study from Canada into the U.S. The funding is part of a broader federal push to validate faster, more measurable behavioral health treatments, including rapid-acting psychedelic therapies.

Why it matters: - The award gives Diamond Therapeutics non-dilutive federal support to expand a phase 2 anxiety trial into the U.S. - The funding could help speed development of rapid-acting behavioral health treatments and generate data on psilocybin-based therapy for generalized anxiety disorder. - ARPA-H’s broader EVIDENT initiative aims to fund up to $139.4 million for new behavioral health therapies.

What happened: - Diamond Therapeutics received a multi-million dollar funding award from ARPA-H for its phase 2 clinical trial in generalized anxiety disorder. - The company will expand an ongoing study in Canada into the U.S. with St. Petersburg, Florida-based Tactical Mind Research Coalition. - Diamond’s U.S. operations are headquartered in Birmingham, Alabama. - The trial is part of ARPA-H’s Evidence-Based Validation & Innovation for Rapid Therapeutics in Behavioral Health, or EVIDENT, initiative.

The details: - The phase 2 study is testing repeated administration of low doses of psilocybin in people with GAD. - Dr. Claudio Soares, director of the Centre for Psychedelics Health and Research in Kingston, Canada, leads the work. - Diamond said the ARPA-H support will help build a more comprehensive dataset to support biomarker identification. - Judy Blumstock, Diamond’s founder and CEO, said the company wants to provide data that supports ARPA-H’s work to validate the safety and effectiveness of rapid-acting therapies including psilocybin. - Michael McDonnell, Diamond’s chief medical officer, said Tactical Mind Solutions will play a key role in the expanded clinical trials, along with other partners. - ARPA-H Director Alicia Jackson said the agency wants objective, predictive measures that show sooner whether a therapy is working for a patient. - Jackson said EVIDENT is intended to reduce failed treatment attempts and help make behavioral health care more measurable and precise.

Between the lines: - The award aligns with a larger federal effort to move psychedelic research from discussion to clinical validation. - The White House issued an executive order on April 18, 2026, to accelerate research into psychedelics for mental health treatments. - The order calls for more clinical research, stronger coordination across regulatory agencies and responsible pathways to patient access. - Diamond’s focus on biomarkers suggests the company is aiming for evidence that could make psychedelic treatment more acceptable to regulators and clinicians.

What’s next: - Diamond will use the new funding to expand the trial and gather U.S.-based data. - The company and its partners will continue working on a larger dataset aimed at verifying efficacy and identifying biomarkers. - ARPA-H’s EVIDENT program will continue awarding funds to support behavioral health therapies.

The bottom line: - Federal funding is helping push Diamond Therapeutics’ psilocybin program from a Canada-based study toward broader U.S. clinical validation.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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