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RecruitingNCT07456696

TSND-201 for PTSD

The registry lists this study as recruiting. Study locations are listed in the United States. Confirm recruitment at each site. It is testing TSND-201 for PTSD.

PTSDDrugOver 18 Years
In plain English

Key information made simple

What is this study testing?

This study is testing whether the Safety and Efficacy of TSND-201 may be useful for adults experiencing ptsd.

What would participation involve?

Participants may receive the Safety and Efficacy of TSND-201, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in the United States.

Who is it mainly for?

This study appears to be mainly for adults with ptsd.

What should you check before joining?

Ask about the dose, safety monitoring, and possible side effects, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.

Your next step

Check the study details

Check the official source, then confirm these points with the research team.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    Where are visits, can any be remote, and how much time is needed?

  • Costs and support

    What costs, reimbursement or compensation apply?

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateStarted: April 2, 2026
Recruitment status
Recruiting
Enrollment listed in the registry
300
Sponsor
Transcend Therapeutics
Sponsor type
Biotech company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
Over 18 Years
Official registry ID
NCT07456696
Official title
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Safety and Efficacy of TSND-201 for the Treatment of PTSD

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Check recruitment and locations

Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.

View official study record (opens in a new tab)

The overall study status can differ from each site's status. Open a country to see its locations and their registry status.

United States · 32 sites
  • Del Sol Research
    Tucson, Arizona
    Site status: Recruiting
  • Preferred Research Partners
    Little Rock, Arkansas
    Site status: Recruiting
  • Kadima Neuropsychiatry
    La Jolla, California
    Site status: Recruiting
  • CalNeuro Research Group
    Los Angeles, California
    Site status: Recruiting
  • Catalina Research Institute
    Montclair, California
    Site status: Recruiting
  • Excell Research
    Oceanside, California
    Site status: Recruiting
  • ATP Clinical Research
    Orange, California
    Site status: Recruiting
  • Inland Psychiatric Medical Group
    San Juan Capistrano, California
    Site status: Recruiting
  • Starlight Clinical Research
    Evergreen, Colorado
    Site status: Recruiting
  • CNS Healthcare
    Jacksonville, Florida
    Site status: Recruiting
  • Segal Trials
    Lauderhill, Florida
    Site status: Recruiting
  • Accel Clinical Research
    Maitland, Florida
    Site status: Recruiting
  • CNS Healthcare
    Orlando, Florida
    Site status: Recruiting
  • Uptown Research Institute
    Chicago, Illinois
    Site status: Recruiting
  • DelRicht - New Orleans
    New Orleans, Louisiana
    Site status: Recruiting
  • Headlands Research - Pharmasite
    Pikesville, Maryland
    Site status: Recruiting
  • Vitalix Clinical
    Worcester, Massachusetts
    Site status: Recruiting
  • Arch Clinical Trials
    Creve Coeur, Missouri
    Site status: Recruiting
  • Midwest Research Group
    Saint Charles, Missouri
    Site status: Recruiting
  • Center for Emotional Fitness/ Lumina Clinical Research Center
    Cherry Hill, New Jersey
    Site status: Recruiting
  • Global Medical Institutes
    Princeton, New Jersey
    Site status: Recruiting
  • Bio Behavioral Health
    Toms River, New Jersey
    Site status: Recruiting
  • Medical Research Network
    New York, New York
    Site status: Recruiting
  • Insight Clinical Trials
    Independence, Ohio
    Site status: Recruiting
  • Flourish Research
    Plymouth Meeting, Pennsylvania
    Site status: Recruiting
  • Suburban Research Associates
    West Chester, Pennsylvania
    Site status: Recruiting
  • Austin Clinical Trial Partners
    Austin, Texas
    Site status: Recruiting
  • Haracec Clinical Research
    El Paso, Texas
    Site status: Recruiting
  • Elevate Clinical Research
    Houston, Texas
    Site status: Recruiting
  • Cedar Clinical Research
    Draper, Utah
    Site status: Recruiting
  • Inner Space Research
    Orem, Utah
    Site status: Recruiting
  • Seattle Neuropsychiatric Treatment Center (NTC)
    Seattle, Washington
    Site status: Recruiting
In practice

For you

Participation may contribute to research. Personal benefit is not guaranteed.

Ask the research team to explain the activities, time commitment, and follow-up involved.

Study sites are listed. Confirm the relevant site and any travel before making plans.

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

FAQ

Questions about this study

What is this study trying to understand?

Based on the public registry summary, this study is trying to understand: This study is evaluating the safety and efficacy of TSND-201 in adults with PTSD. Eligible participants will enter a 4-week Treatment Period where they will be randomized 1:1:1 to receive one of two doses of TSND-201 or placebo, once per week. Following the Treatment Period,. The study team can confirm the exact objective and what it means for you.

Does this study involve a medication?

This appears to be a medication / drug study involving TSND-201, Placebo. Phase 3 studies are usually larger and aim to confirm effectiveness and safety in a broader group.

Who might this study be for?

This study may concern people with ptsd; age range: Over 18 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.

What would I likely need to do?

You may need to take a study treatment and have regular medical follow-up. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.

What side effects, interactions, or treatment changes should I check?

If the study involves a medication, ask whether it is already approved, experimental, or being tested for a new use. Check possible side effects, interactions with current treatment, dose changes, monitoring, and what happens if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.

Will I need to travel or attend in-person visits?

The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.

Who is behind this study?

This study is sponsored by Transcend Therapeutics, which appears to be a biotech company. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.

Can I still join this study?

The public registry lists this study as recruiting. Individual sites may have different statuses. The research team must confirm whether a site is open and whether you meet the criteria.

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