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New pill for brain disorders takes first safety step

NCT ID NCT06300398

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This early-stage study tested a new oral drug called IAMA-6 in 72 healthy adults to see if it is safe and how the body processes it. The drug is being developed for neurodevelopmental disorders, but this trial did not treat any disease. Researchers monitored side effects, vital signs, and lab results to gather initial safety data.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

72 people

The number who actually took part.

Started

Jan 2024

Finished

Nov 2024

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 55 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Healthy male and female subjects. * Aged between 18 and 55 years. * Written informed consent; willing and able to comply with procedures. * Females will not be pregnant or lactating, and females of childbearing potential and males will agree to use contraception. * Body mass index of 18.0 to 30.0 kg/m2, inclusive; and a total body weight \>50 kg up to a maximum of 110 kg. * The subject must be willing to return to the study centre for study treatment and study-related follow-up procedures as required by the protocol. Exclusion Criteria: * Current or past history of a clinically significant (as judged by the Investigator) cardiovascular, cerebrovascular, respiratory, gastrointestinal, hematologic, renal, hepatic, immunologic, metabolic, urologic, neurologic, dermatologic, psychiatric, or other major disease/condition, as determined by the Principal Investigator or Designee. * Any history of central nervous system problems (e.g. epilepsy, head injury, loss of consciousness). * Any history of malignancy in the previous 5 years involving any organ system (other than localised basal cell carcinoma of the skin). * Body Mass Index: \<18 kg/m2 , or \>30 kg/m2. * Abnormal vital signs, including known history of hypertension, resting oxygen saturation \<95% by pulse oximetry. * ECG at screening or on Day -1 showing QTcF interval \>450 msec in males or \>470 msec in females, or presence of any clinically significant dysrhythmia. * History of hypersensitivity to any medicinal product(s) or severe hypersensitivity/anaphylaxis with unclear aetiology. * Any clinically significant abnormal chemistry values. * Any clinically significant abnormal haematology values. * Blood donation within the past 3 months. * Seropositivity for HBsAg, HCV, HIV 1, or HIV 2. * Has a positive nasopharyngeal test for SARS-CoV-2 within 48h before unit admission. * If female, has a positive highly sensitive urine pregnancy test at Screening or Day 1. * If female and of child-bearing potential, and not meeting the approved criteria for highly effective methods of birth control. * Receipt of any Investigational Drug within the past 6 months. * Use of prescription medication within 14 days prior to dosing and antibiotics within 30 days prior to dosing. * Intake of OTC preparations, vitamins, minerals, herbal remedies within 48h prior to dosing. * Current smokers or history of smoking in previous 6 months. * Current or history of drug, alcohol, nicotine abuse, or excessive coffee (\>5 cups/day) or tea drinking (\>5 cups/day). * Inadequate comprehension of study risks and requirements.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Centro Ricerche Cliniche Di Verona S.r.l.

    Verona, Italy

More trials for these conditions

Other studies related to the condition(s) this trial covers.