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TerminatedNCT02477748

MDX (Metadoxine Immediate-release/Slow-release, Bilayer Tablet) 1400 mg Compared With Placebo for ADHD

This study was terminated in the United States and in Israel. It is testing MDX (Metadoxine Immediate-release/Slow-release, Bilayer Tablet) 1400 mg Compared With Placebo for ADHD.

ADHDDrugFrom 18 Years to 55 Years

The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

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In plain English

Key information made simple

What is this study testing?

This study is testing whether MDX 1400 mg Daily Compared With Placebo may be useful for adults experiencing ADHD.

What would participation involve?

Participants may receive MDX 1400 mg Daily Compared With Placebo, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in Israel and in the United States.

Who is it mainly for?

This study appears to be mainly for adults with ADHD.

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 dateJune 2015
Recruitment status
Terminated
Enrollment listed in the registry
283
Sponsor
Alcobra Ltd.
Sponsor type
Other organization
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, Israel
Age range
From 18 Years to 55 Years
Official registry ID
NCT02477748
Official title
A 10-week Randomized, Multicenter, Double-blind, Parallel, Fixed-dose Study of MDX (Metadoxine Immediate-release/Slow-release, Bilayer Tablet) 1400 mg Compared With Placebo in Adults With Attention Deficit Hyperactivity Disorder (ADHD)

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.

Israel · 2 sites
  • Rambam Medical Center
    Haifa
    Site status: Not listed — confirm with the team
  • Geha Medical Centre
    Petah Tikva
    Site status: Not listed — confirm with the team
United States · 36 sites
  • Harmonex, Inc.
    Dothan, Alabama
    Site status: Not listed — confirm with the team
  • Pharmacology Research Institute
    Los Alamitos, California
    Site status: Not listed — confirm with the team
  • Pharmacology Research Institute
    Newport Beach, California
    Site status: Not listed — confirm with the team
  • Artemis Institute for Clinical Research
    San Diego, California
    Site status: Not listed — confirm with the team
  • University of California, San Francisco
    San Francisco, California
    Site status: Not listed — confirm with the team
  • MCB Clinical Research Centers
    Colorado Springs, Colorado
    Site status: Not listed — confirm with the team
  • Connecticut Clinical Research
    Cromwell, Connecticut
    Site status: Not listed — confirm with the team
  • Coastal Connecticut Research
    New London, Connecticut
    Site status: Not listed — confirm with the team
  • Sarkis Clinical Trials
    Gainesville, Florida
    Site status: Not listed — confirm with the team
  • Clinical Neuroscience Solutions
    Jacksonville, Florida
    Site status: Not listed — confirm with the team
  • CNS Healthcare
    Orlando, Florida
    Site status: Not listed — confirm with the team
  • Miami Research Associates
    South Miami, Florida
    Site status: Not listed — confirm with the team
  • Institute for Advanced Medical Research
    Alpharetta, Georgia
    Site status: Not listed — confirm with the team
  • Goldpoint Clinical Research
    Indianapolis, Indiana
    Site status: Not listed — confirm with the team
  • Lake Charles Clinical Trials
    Lake Charles, Louisiana
    Site status: Not listed — confirm with the team
  • Kennedy Krieger Institute
    Baltimore, Maryland
    Site status: Not listed — confirm with the team
  • Rochester Center For Behavioral Medicine
    Rochester Hills, Michigan
    Site status: Not listed — confirm with the team
  • St. Charles Psychiatric Associates - Midwest Research Group
    Saint Charles, Missouri
    Site status: Not listed — confirm with the team
  • Premier Psychiatric Research Institute
    Lincoln, Nebraska
    Site status: Not listed — confirm with the team
  • Center for Emotional Fitness
    Cherry Hill, New Jersey
    Site status: Not listed — confirm with the team
  • Global Medical Institutes, LLC, Princeton Medical Institute
    Princeton, New Jersey
    Site status: Not listed — confirm with the team
  • The Medical Research Network
    New York, New York
    Site status: Not listed — confirm with the team
  • Richard H Weisler, MD, PA
    Raleigh, North Carolina
    Site status: Not listed — confirm with the team
  • Neuro-Behavioral Clinical Research, Inc.
    Canton, Ohio
    Site status: Not listed — confirm with the team
  • IPS Research Company
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • Village Clinical Research Inc
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • Summit Research Network
    Portland, Oregon
    Site status: Not listed — confirm with the team
  • Suburban Research Associates
    Media, Pennsylvania
    Site status: Not listed — confirm with the team
  • Carolina Clinical Research, Inc.
    Charleston, South Carolina
    Site status: Not listed — confirm with the team
  • Clinical Neuroscience Solutions
    Memphis, Tennessee
    Site status: Not listed — confirm with the team
  • BioBehavioral Research of Austin at Specialty Clinic of Austin
    Austin, Texas
    Site status: Not listed — confirm with the team
  • Bayou City Research
    Houston, Texas
    Site status: Not listed — confirm with the team
  • Psychiatric & Behavioral Solutions
    Salt Lake City, Utah
    Site status: Not listed — confirm with the team
  • NeuroScience, Inc. (NSI)
    Herndon, Virginia
    Site status: Not listed — confirm with the team
  • Summit Research Network(Seattle)LLC
    Seattle, Washington
    Site status: Not listed — confirm with the team
  • Dean Foundation - Middleton
    Middleton, Wisconsin
    Site status: Not listed — confirm with the team

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Study ID: NCT02477748. We help you review the study, but cannot decide medical eligibility.
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?

This study is exploring medication or study treatment for people with adhd. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.

Does this study involve a medication?

This appears to be a medication / drug study involving MDX, 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 adhd; age range: From 18 Years to 55 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 Alcobra Ltd., which appears to be another type of organization. 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 not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

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