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New drug LY3451838 tested in healthy people for safety

NCT ID NCT03692949

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This early-stage trial tested the safety and how the body handles a new drug called LY3451838 in 53 healthy adults. Participants received either a single dose of the drug into a vein or under the skin, or a placebo. The main goal was to check for side effects and measure drug levels in the blood.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
LY3451838

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

53 people

The number who actually took part.

Started

Dec 2018

Finished

Feb 2020

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

21 to 65 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: * Male participants must adhere to contraception restrictions * Female participants must be of non-childbearing potential due to: * Menopause: spontaneous amenorrhea for at least 12 months not induced by a medical condition such as anorexia nervosa and not taking medications that induced the amenorrhea (e.g., oral contraceptives, hormones, gonadotropin releasing hormone, anti-estrogens, selective estrogen receptor modulators, or chemotherapy) * Surgical sterilization * Have a body mass index of 18 to 35 kilograms per square meter (kg/m²) * Have clinical laboratory test results within normal reference range or with acceptable deviations * Have an estimated glomerular filtration rate greater than or equal to (≥) 60 milliliters per minute per 1.73 meters squared (mL/minute/1.73 m²) of body surface area * Have venous access sufficient to allow for blood sampling Exclusion Criteria: * Are currently enrolled in or discontinued from a clinical trial within the last 30 days, or have previously completed or withdrawn from this study * Have a history or presence of medical illness including, but not limited to, any cardiovascular, hepatic, respiratory, hematological, renal, endocrine, psychiatric or neurological disease, or any clinically significant laboratory abnormality * Have history of or presence of uncontrolled asthma, significant atopy, or significant rheumatological or autoimmune diseases * Have had lymphoma, leukemia, or any malignancy within the past 5 years, or breast cancer within the past 10 years (with some exceptions) * Have used, or intend to use some prescription or over the counter medications, including herbal medications within 14 days prior to dosing * Have an abnormality in the 12-lead electrocardiogram (ECG) or Fridericia's corrected QT (QTcF) * Show evidence of human immunodeficiency virus (HIV) and/or positive human HIV antibodies, hepatitis C and/or positive hepatitis C antibody, or hepatitis B and/or positive hepatitis B surface antigen * Have donated blood of more than 450 milliliters (mL) within the last 3 months * Are unwilling to stop alcohol consumption while resident in the Clinical Research Unit (CRU) * Have an average weekly alcohol intake that exceeds 21 units per week for males and 14 units per week for females (1 unit = 12 ounces (oz) or 360 mL of beer; 5 oz or 150 mL of wine; 1.5 oz or 45 mL of distilled spirits) * Current smoker of more than 10 cigarettes or equivalent per day and unable to stop smoking while in the CRU * Have an abnormal blood pressure * Have clinically significant proteinuria or hematuria * Positive findings for known drugs of abuse * Have received treatment with biologic agents within 3 months or 5 half-lives (whichever is longer) * Have clinically significant allergies, or intolerance to corticosteroids, or severe post treatment hypersensitivity reactions

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Lilly Centre for Clinical Pharmacology

    Singapore, 138623, Singapore

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