Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Healthy volunteers help scientists measure drug absorption

NCT ID NCT07519525

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 study looked at how the body processes a drug called LY4064809. Seven healthy adults received the drug by mouth and by IV to compare how much enters the bloodstream. The goal was to understand the drug's absorption, not to treat any disease. Participants stayed at a research center for 14 days.

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

7 people

The number who actually took part.

Started

Mar 2026

Finished

May 2026

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: * Must be healthy as shown by medical history, physical examination, laboratory tests and heart monitoring * Must have normal blood pressure and pulse rate * Must have a history of a minimum of 1 bowel movement per day * Must have body mass index (BMI) between 18 and 32 kilograms per square meter (kg/m2) * Must be healthy men or healthy women who are not of childbearing potential * Healthy men with partners who can become pregnant must remain abstinent or use contraceptives consistent with local regulations Exclusion Criteria: * Must not have a significant history or presence of metabolic disease, heart, liver, gallbladder, bile ducts, digestive, blood or nervous system disorders that could affect the way the body absorbs and processes the study drug * Must not have an abnormal electrocardiogram (ECG) * Must not have a history of major surgery within 30 days of entering study * Must not have a history of cancer within 5 years of screening * Must not have known allergies to LY4064809 or related compounds * Must not have history of multiple or severe drug reactions or allergies which required treatment with steroids or epinephrine * Must not have history or presence of psychiatric conditions that would prevent the participant from following study instructions. * Must not use medications, except acetaminophen within 14 days of the first dose of LY4064809 and during the clinic stay * Must not have participated in and been dosed in more than 2 radiolabeled drug studies in the last 12 months * Must not have had exposure to significant diagnostic, therapeutic or employment-related radiation within 12 months * Must not have participated in any other radiolabeled investigational study drug trial within 6 months prior to admission. * Must not show evidence of human immunodeficiency Virus (HIV) infection or positive HIV-1 and HIV-2 antibodies * Must not have evidence of Hepatitis C virus (HCV) infection or a positive HCV antibody test. * Must not have evidence of Hepatitis B virus (HBV) infection or a positive Hepatitis B surface antigen (HBsAg) * Must not have alcohol intake deemed significant by the investigator * Must not use tobacco, smoking-cessation products, e-cigarettes (nicotine and non-nicotine), or nicotine products within 90 days prior to LY4064809 administration and discharge from the clinical research unit (CRU) or early termination (ET)

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Healthy are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

Contacts and locations

Locations

  • Fortrea Clinical Research Unit Inc. - Madison

    Madison, Wisconsin, 53704-2526, United States

More trials for these conditions

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