Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:16 AM
Ignite Modification Date:
2025-12-25 @ 3:16 AM
NCT ID:
NCT01860105
Eligibility Criteria:
Inclusion Criteria
* Healthy males or females 18 to 45 years of age, inclusive.
* Provide written informed consent for genetic testing and written informed consent for the study before initiation of any study related procedures
* Affiliated to the French social security system
* Screening and baseline Fridericia's correction (QTcF) interval \< 450 msec and baseline heart rate between 50 and 100 bpm (inclusive)
Exclusion Criteria:
* Known or suspected hypersensitivity or allergy to clopidogrel, Captisol, PLAVIX® , or its excipients
* Body mass index \<20 or \> 30 kg/m²
* Inability to communicate with the investigator or comply with study related procedures, or high likelihood of being lost to follow up
* Known or suspected pregnancy or lactating female
* Medical history, physical examination including 12-lead ECG or laboratory evaluation conducted at the screening visit with results indicative of any disease or condition which might compromise the hematologic, cardiovascular, pulmonary, renal, gastrointestinal, hepatic, or central nervous system; or other conditions that may interfere with the absorption, distribution, metabolism or excretion of study drug, or would place the subject at increased risk
* Tobacco product use within the last 6 months prior to dosing
* Platelet count \< 150,000/µL
* A personal or family history of coagulation or bleeding disorders or reasonable suspicion of vascular malformations
* Active pathological bleeding such as peptic ulcer or intracranial hemorrhage
* Positive screen for Hepatitis B (Hepatitis B Surface Antigen HBsAg), Hepatitis C (Hepatitis C Antibody), or HIV (anti-HIV 1/2)
* Received an investigational drug within a period of 30 days or 5 half-lives, whichever is longer, prior to enrollment in the study
* Use of aspirin, other non-steroidal anti-inflammatory drugs, CYP3A4 inhibitors (ketoconazole), CYP2C19 inhibitors (eg, omeprazole) or other drugs known to affect platelet function or coagulation within 14 days prior to receiving study drug (MDCO-157 or oral clopidogrel)
* Grapefruit within 10 days prior to receiving study drug (MDCO-157 or PLAVIX®)
* Use of any over-the-counter medication, including herbal products, within 7 days prior to administration of study drug (MDCO-157 or PLAVIX®), except for up to 2 grams of acetaminophen per day for up to 3 days for pain control
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT01860105
Study Brief:
Protocol Section:
NCT01860105