Psyence Biomedical's Subsidiary, Psyence Australia, Receives Human Research Ethics Committee (HREC) Approval To Initiate Phase IIb Study
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Psyence Biomedical's subsidiary, Psyence Australia, has received approval from the Human Research Ethics Committee to begin a Phase IIb study on the use of nature-derived psilocybin for treating Adjustment Disorder in palliative care patients recently diagnosed with cancer. This study addresses a significant need, given the estimated 56.8 million people requiring palliative care worldwide annually, many of whom experience considerable psychosocial distress post-diagnosis.

March 06, 2024 | 12:06 pm
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Psyence Biomedical's approval to initiate a Phase IIb study on psilocybin for Adjustment Disorder in palliative care could position the company as a leader in psychedelic-assisted therapies, potentially boosting investor confidence and stock value.
The approval for Psyence Biomedical's subsidiary to conduct a Phase IIb study is a significant regulatory milestone that could enhance the company's reputation in the burgeoning field of psychedelic-assisted therapies. Given the large potential market indicated by the 56.8 million people requiring palliative care annually, this development could lead to increased investor interest and a positive impact on PBM's stock price in the short term.
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