Now Enrolling Kirsten Hirst Now Enrolling Kirsten Hirst

Depression • MindMed

This study is designed to evaluate the efficacy of a single dose of 100 µg of MM-120 (D-lysergic acid diethylamide D-tartrate), versus placebo, for the treatment of depression symptoms.

This study is sponsored by Mind Medicine, Inc.

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Now Enrolling Kirsten Hirst Now Enrolling Kirsten Hirst

Depression • Cybin

For adults with a diagnosis of Major Depressive Disorder (MDD) currently experiencing a Major Depressive Episode (MDE).

The goal of this study is to evaluate the efficacy, safety, and tolerability of CYB003, compared to placebo, in treating symptoms of MDD in adult participants.

This study is sponsored by Cybin.

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Now Enrolling Kirsten Hirst Now Enrolling Kirsten Hirst

PTSD • Transcend

For adults living with Post Traumatic Stress Disorder (PTSD)

The purpose of this study is to assess the efficacy, safety, and tolerability of TSND-201 for the treatment of PTSD symptoms compared to placebo

This study is sponsored by Transcend Therapeutics, Inc.

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Now Enrolling Kirsten Hirst Now Enrolling Kirsten Hirst

Depression • J&J

People with depression often struggle to fall asleep or stay asleep, and ongoing sleep problems can also increase feelings of sadness or hopelessness. Adults being treated for depression may qualify to participate in an in-home sleep study.

Adults with depression are needed to participate in a sleep study from their own homes.

No insurance is required for participation.

This study is sponsored by Autobahn J&J, Inc

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Now Enrolling Kirsten Hirst Now Enrolling Kirsten Hirst

Depression • Autobahn

For adults with a diagnosis of Major Depressive Disorder (MDD) who continue to experience symptoms despite being on an antidepressant medication.

The goal of this study is to evaluate the efficacy, safety, and tolerability of ABX-002, an oral thyroid hormone receptor-beta (TRβ) agonist, as an adjunctive treatment for MDD. Participants will receive either ABX-002 or placebo in addition to their current antidepressant for approximately six weeks.

This study is sponsored by Autobahn Therapeutics, Inc.

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