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Gage will oversee clinical strategy and execution for Psilera’s upcoming Phase 1 first-in-human trial of PSIL-006.
August 27, 2026
By: Charlie Sternberg
Psilera Inc., a biopharmaceutical company pioneering next-generation neuroplastogens and psychedelic therapies, has appointed Allyson Gage, PhD, as Vice President, Clinical Development, where she will oversee the clinical development strategy and operational execution of the upcoming Phase 1 first-in-human clinical trials of Psilera’s lead asset, PSIL-006.
Gage brings over 25 years of experience to Psilera, with a track record of advancing numerous compounds through FDA IND approval. Her expertise in biomarker identification and evaluation in CNS indications, small molecules, biologics, and cell therapies ideally positions her to lead Psilera’s Phase 1 trial as VP, Clinical Development.
“Psilera is engineering tomorrow’s therapies by leveraging the potential therapeutic power of neuroplastogens,” states Gage. “I’m honored to join this team and to help guide PSIL-006 through the clinical milestones that will bring these treatments to the patients who need them.”
The PSIL-006 Phase 1a clinical trial will evaluate safety, tolerability, and key biomarkers in human subjects, supporting its development for neuropsychiatric conditions such as depression, addiction, PTSD, and neurodegeneration.
“I am thrilled to partner with Dr. Gage once again as we advance the neuroplastogen pipeline at Psilera,” said Magali Haas, MD-PhD, CMO of Psilera. “Allyson brings an exceptional combination of CNS drug development expertise and leadership with her impressive track record navigating the complex path from first-in-human studies through pivotal trials and ultimately regulatory approval.”
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