New drug CBP-4888 passes first safety check in healthy volunteers
NCT ID NCT05881993
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new drug called CBP-4888 in 45 healthy women who were not pregnant. The goal was to see if the drug is safe and how the body processes it. Participants received either a single dose of the drug or a placebo. The study did not aim to treat any disease, only to gather early safety information.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
45 people
The number who actually took part.
- Started
-
May 2023
- Finished
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May 2024
- 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
-
18 to 50 years
- Sex
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Female participants only
- 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: * Healthy non-pregnant female subjects * Body mass index (BMI) ≥ 18.5 and ≤ 35.0 kg/m2 * Medically healthy, defined as having no clinically significant abnormal screening results including clinical laboratory evaluations, medical history, vital signs, ECG, and physical examination as deemed by the Investigator. Exclusion Criteria: * Screening blood pressure \< 100/60 mmHg or \> 140/90 mmHg * Screening heart rate that is \< 40 bpm or \> 99 bpm * Clinically significant ECG abnormality at screening * Used prescription medication within 14 days prior to dosing * Used over the counter (OTC) medications (including herbal products, nutritional supplements, dietary supplements, and/or vitamins) within 7 days prior to dosing * Donated blood or had significant blood loss within 56 days prior to dosing
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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.
Contacts and locations
Locations
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Comanche Biopharma Clinical Research Site #1
San Antonio, Texas, 78217, United States
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