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KOASTAL Study for Those Experiencing Depression
Protocol: STUDY00008371
Full Title
Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effects of Oral NMRA-335140 versus Placebo in Participants with Major Depressive Disorder
Description
The University at Buffalo (UB) Department of Psychiatry is looking for adults living with depression for a clinical trial. The research team is interested in studying how effective a new medicine is at treating symptoms of depression.

Following a month-long preparation phase, they will be randomly assigned (which happens by chance, like flipping a coin) to receive either the study medicine or a placebo (which looks like the study medicine but does not contain any active ingredients) for 6 weeks. Participants will then either have additional follow-up visits in the months to follow to conclude their involvement in the study, or enter into a separate follow-up study for over a year.

Throughout this study, participants will attend in-person study visits and complete surveys and lab tests. Participants will earn between $75 - $150 depending on the study visit.
Compensation: Yes
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Compensation may include cash, checks, gift cards, debit cards, or incentives like gift baskets, technology items, or merchandise.
Eligibility
-Adults aged 18 to 65 years old
-Have been told by a doctor that you have depression
-Have had symptoms of depression for 1-12 months
-Are not pregnant or breast feeding
Age Group: Adults
Principal Investigator: BETH SMITH
ClinicalTrials.gov: Open Study
Contact(s)
Christopher Suchan
cssuchan@buffalo.edu
+1 716-668-9024

Want to Learn More?

Let us know how the study team can reach you. If you do not hear back within 2 business days, then reach out to the study team directly at the contact information above and someone will assist you.

Your information will be shared only with the research study team and administrative staff for recruitment and will remain confidential. Your information will be stored until study recruitment is closed. Should you no longer want this information to be provided in the aforementioned ways, please contact the study team directly.

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