New drug ISM4808 put to the test in healthy volunteers
NCT ID NCT07415304
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-stage study tests the safety and tolerability of a new oral drug called ISM4808 in 86 healthy adults aged 18-55 in China. Participants receive either the drug or a placebo, and researchers monitor for side effects and how the drug moves through the body. The goal is to gather safety data, not to treat any disease.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 86 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 55 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * • Able and willing to provide written informed consent and comply with all study procedures. * Healthy male or female adults aged 18 to 55 years at the time of informed consent. * Body mass index (BMI) 19-26 kg/m²; body weight ≥50 kg (males) and ≥45 kg (females). * Medically healthy with no clinically significant abnormalities in medical history, physical examination, vital signs, laboratory tests, or 12-lead ECG, as determined by the investigator. * Women of childbearing potential and male subjects with partners of childbearing potential must agree to use effective contraception from screening through 3 months after the last dose of investigational product. Exclusion Criteria: * History or presence of any clinically significant disease (including cardiovascular, neurological, psychiatric, gastrointestinal, hepatic, renal, hematologic, endocrine, or immune disorders) that may interfere with study participation or data interpretation. * Personal or family history of clinically significant cardiac disease, including QT prolongation, torsades de pointes, myocardial infarction, heart failure, or sudden cardiac death. * Use of medications known to prolong QT/QTc interval or treatment for clinically significant cardiac conditions. * Screening 12-lead ECG abnormalities, including QTcF \>450 ms (males) or \>470 ms (females), PR interval \>210 ms, QRS duration \>110 ms, clinically significant arrhythmias, or uncontrolled hypertension. * Participation in another interventional clinical trial or receipt of any investigational drug within 3 months prior to first dosing. * Blood donation or significant blood loss (≥400 mL) within 3 months prior to first dosing. * Pregnant or breastfeeding women, or positive pregnancy test at screening or prior to dosing. * Positive tests for HBsAg, HCV antibody, HIV antibody, or syphilis. * History of drug or alcohol abuse, positive drug screen, or inability to abstain from alcohol, nicotine, or prohibited substances during the study. * Use of prescription or non-prescription medications, herbal products, supplements, or vaccines within 28 days prior to dosing, unless approved by the investigator. * Any condition that, in the opinion of the investigator, would make the subject unsuitable for participation in the study.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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