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:
2025-12-24 @ 10:50 PM
Ignite Modification Date:
2025-12-24 @ 10:50 PM
NCT ID:
NCT02211469
Eligibility Criteria:
For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com.
Inclusion Criteria:
* Healthy male subjects as determined by medical history, physical examination, vital signs, 12-lead electrocardiogram (ECG), and clinical laboratory evaluations will be eligible to participate in the study
* Men ages 18 to 49 years, inclusive
Exclusion Criteria:
* Any acute or chronic medical illness judged to be clinically-significant by the Investigator and/or Sponsor medical monitor
* Presence of fecal occult blood at screening
* History of prolonged occupational exposure to organic solvents or pesticides
* History of vitamin B12 deficiency and/or achlorhydria; or a vitamin B12 level at screening \<lower limit of normal (LLN), confirmed by repeat test
* History of Guillain-Barré Syndrome
* Past or current history of central or peripheral neuropathies, or past or current symptoms of sustained or recurrent paresthesias (tingling), numbness, or neuropathic pain (burning, aching or stabbing) in any extremities. Note: Experiencing an extremity "falling asleep" occasionally is not be exclusionary
* Clinically significant abnormality in the neurological exam at baseline (predose)
* Clinically significant nerve electrophysiology abnormalities at baseline (predose)
* Any history of testicular or epididymal disease/disorder
* Clinically significant abnormality on ophthalmologic exam or any findings suggesting an increased risk of macular edema at baseline (predose)
* History of hypothyroidism or carpal tunnel syndrome
* Subjects with history of diabetes mellitus
* Subjects with history of any type of heart disease, including ischemia, infarction, arrhythmias, hypertension, atrioventricular block of any degree, bradycardia, syncope, clinically significant ECG abnormalities, or any congenital heart disease
* Subjects with any acute or chronic bacterial, fungal or viral infection within the last 3 months prior to screening, as well as any febrile illness of unknown origin within 14 days of screening
* Subjects who have received any live vaccines within 1 month of study drug administration or who plan to have a live vaccine at any time during the study
* Positive test for tuberculosis at screening (QuantiFERON® GOLD)
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
49 Years
Study:
NCT02211469
Study Brief:
Protocol Section:
NCT02211469