Lenexa, Kansas 66219

  • Healthy Participants

Purpose:

The purpose of this study is to evaluate the safety, tolerability, drug levels, and drug effects of BMS-986308 compared to placebo in healthy participants.


Criteria:

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - In good health, as determined by no clinically significant deviations from normal in medical history, physical examination, electrocardiograms (ECGs), and clinical laboratory determinations - Body mass index (BMI) of 18.0 kg/m^2 to 32.0 kg/m^2, inclusive, at screening. BMI = weight (kg)/height (m)^2 - Normal renal function at screening (and study admission) as evidenced by an estimated glomerular filtration rate (eGFR) ≥ 80 mL/min/1.732 m^2 calculated with the Chronic Kidney Disease Epidemiology Collaboration formula - Must agree to follow specific methods of contraception, if applicable Exclusion Criteria: - Women who are of childbearing potential or breastfeeding - Any significant acute or chronic medical illness - Presence or need for urinary catheterization, urinary tract abnormality, or disorder interfering with urination - History of tinnitus or hearing impairment, including deafness - History or risks factors for Torsade de Pointes and Long QT syndrome (such as electrolyte imbalances, etc) - History of, or active, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection - Consumption of caffeine or xanthine-containing food or beverages within 72 hours prior to study treatment administration - Use of any prescription drugs or over-the-counter (OTC) acid controllers within 4 weeks prior to study treatment administration except those medications cleared by the Medical Monitor - Use of any other drugs, including OTC medications within 1 week and herbal preparations, within 2 weeks prior to study treatment administration except those medications cleared by the Medical Monitor - Use of diuretics (loop diuretics, thiazide diuretics, potassium-sparing diuretics [spironolactone, amiloride]), oral calcium, potassium or magnesium supplements (including multi-vitamins) or use of non-steroidal anti-inflammatory drugs within 72 hours of the first study treatment - Use of concomitant medications that are strong inhibitors or inducers of cytochrome CYP3A4 or OATP administered within 2 weeks prior to study treatment administration and throughout the study - Consumption of any nutrients known to modulate cytochrome P450 (CYP) enzymes activity (eg, grapefruit, or grapefruit juice,pomelo juice, star fruit, or Seville [blood] orange products) within 14 days prior to first administration of study treatment - Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECG, or clinical laboratory determinations beyond what is consistent with the target population of healthy volunteers - History of allergy to furosemide, sulfonamides, other loop diuretics (furosemide cohort only), BMS-986308 or related compounds, components of the suspension or solution, including hydroxypropylmethylcellulose Other protocol-defined inclusion/exclusion criteria apply


NCT ID:

NCT04763226


Primary Contact:

Study Director
Bristol-Myers Squibb
Bristol-Myers Squibb

Recruiting sites have contact information. Please contact the sites directly. If there is no contact information,
Phone: please email:
Email: Clinical.Trials@bms.com


Backup Contact:

First line of the email MUST contain NCT # and Site #.


Location Contact:

Lenexa, Kansas 66219
United States

Site 0001

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 20, 2021

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