First in Humans Study of JDTic

Stopped early · Phase 1

Conditions studied: Cocaine Dependence

In brief

This is the first study to be conducted in humans for JDTic, a new chemical entity, with evaluations focusing on the safety, tolerability, and pharmacokinetics (PK) of JDTic following administration of single oral doses. JDTic is a novel, selective κ opioid receptor antagonist and is currently being developed by RTI International as a potential pharmacotherapy to treat cocaine dependence. This study has the possibility of identifying the maximum tolerated dose in humans and a surrogate measure of JDTic pharmacodynamic (PD) activity. Data from this study will be used to plan for and define dose ranges for subsequent studies, as well as to identify potential indicators of JDTic pharmacological activity.

Key facts

Study ID

NCT01431586

Run by

RTI International

People needed

24

Last updated by the study team

2012-05-10

Who can join

Age: 18 and older, up to 50. Sex: male. Healthy volunteers: accepted.

You may qualify if…

• Subject provides signed and dated, written informed consent before any study-specific procedures are performed, including washout of any medications. Subjects will be asked to meet the food, beverage and physical activity restrictions required for the screening visit prior to signing consent.
• Subject is a healthy adult male aged 18 to 50 years, inclusive, at the time of consent.
• Subject has a body weight of at least 50 kg and a body mass index (BMI) in the range of 18 to 30
• Subject has a negative prestudy urine drug screen and no history of use of illicit drugs within 12 months of the screening visit or other substances of abuse within 12 months of the screening visit.
• Subject has not used tobacco for at least 90 days prior to screening.
• Subject has no history of any cardiovascular disease and no clinically significant ECG results at screening.
• Subject is negative for hepatitis C (HCV) antibodies, hepatitis B (HBV) surface antigen, and human immunodeficiency virus (HIV) at screening.
• Subject is in good general health in the opinion of the Clinic Principal Investigator and as determined by medical history, physical examination, orthostatic vital signs (supine, sitting, and standing blood pressure and heart rate; supine respiratory rate and oral temperature), 12-lead ECG, and clinical laboratory tests at screening. Additionally, the subject's clinical laboratory test results must meet the following criteria:
• Within normal limits: Reticulocyte count
• Within upper limit of normal and not clinically significantly below the lower limit of normal: Aspartate aminotransferase (AST) Alanine aminotransferase (ALT) Gamma glutamyl transferase (GGT) Prothrombin time (PT) Activated partial thromboplastin time (aPTT) Serum troponin I Blood urea nitrogen (BUN) Creatinine Bilirubin, total Alkaline phosphatase Creatine kinase Lactate dehydrogenase (LDH)
• No clinically significant abnormalities: Sodium Protein, total Calcium Chloride Phosphorus Albumin Globulin Cholesterol Triglycerides Red blood cells (RBC) White blood cells (WBC) Hematocrit Hemoglobin Platelets Glucose Potassium WBC differential RBC indices Uric acid Urinalysis
• Subject is willing to use barrier contraception with spermicide during sexual intercourse and is also willing to not donate sperm while enrolled in this study and for at least 90 days after receiving his dose of study drug.
• Subject is willing and able to comply with study instructions and restrictions and is available to complete the study assessments as required by the protocol
• Subject is fluent in English.

You may not qualify if…

• Subject has a history or evidence of hepatic, GI, renal, respiratory, ophthalmic, cardiovascular, hematologic, endocrine/metabolic, neurologic, immunologic, oncologic, or psychiatric illness or significant abnormalities; OR other condition(s)/surgical intervention(s) known to interfere with the absorption, distribution, metabolism, or excretion of drugs.
• Subject has a clinically significant abnormal ECG at screening or prior to dosing. Multiple premature atrial contractions or multiple premature ventricular contractions (PVCs), with the exception of non-clinically significant unifocal PVCs, are considered clinically significant, as are bundle branch blocks, second or third degree heart block, or any arrhythmia other than respiratory sinus arrhythmia.
• Subject has one or more ECG parameters outside the following ranges at Screening or just prior to dosing:
• Heart rate less than 55 or greater than 100 beats per minute (bpm), PR interval less than 120 or greater than 180 msec, QRS duration less than 70 or greater than 100 msec, QT interval (Bazett) greater than 420 msec
• One or more of the Subject's supine vital signs are outside the ranges specified below:
• Systolic blood pressure: 90-140 mmHg, inclusive
• Diastolic blood pressure: 60-90 mmHg, inclusive
• Heart rate: 55-100 beats per minute (bpm), inclusive
• Respiratory rate: 12-20 breaths per minute, inclusive
• Oral temperature: 97.0-99.7 degrees Fahrenheit, inclusive
• Subject has a history or current evidence of early cardiac repolarization.
• Subject has a history or family history of QT prolongation, arrhythmia, or uncontrolled hypertension.
• Subject has a history of seizure, head injury, neurosurgery or brain trauma, or a family history of nontraumatic seizure.
• Subject has an infection of any type or clinically significant abnormality identified by the screening medical or laboratory evaluations.
• Subject has consumed alcohol within 48 hours prior to the screening visit or is unwilling to discontinue alcohol consumption within 48 hours of being admitted to the clinic.
• Subject has a history of significant alcohol consumption, defined as an average weekly intake of greater than 21 units or an average daily intake of greater than 3 units, with 1 unit equivalent to 1 can or bottle (12 oz) of beer, or 1 measure (1.5 oz) of spirits, or 1 glass (5 oz) of wine.
• Subject is unwilling to discontinue the consumption of caffeine containing beverages 72 hours prior to clinic admission.
• Subject has consumed or is unwilling to abstain from consuming grapefruit or grapefruit-, poppy seed-, or quinine-containing substances, within 14 days of clinic admission.
• Subject has used a prescription medication within 30 days prior to receiving his dose of study medication; or has used nonprescription medications, dietary supplements, or herbal supplements within 14 days of receiving his dose of study medication, with the exception of acetaminophen, which may be taken up to 24 hours prior to dosing.
• Subject has had any acute GI illness or infection within 14 days prior to receiving his dose of study medication.
• Subject has participated in an investigational trial within 45 days prior to receiving his first dose of study medication.
• Subject is unable to donate blood, has a clotting disorder(s), or has donated blood or lost a significant amount of blood within 8 weeks prior to screening.
• Subject has an unexplained weight loss or gain (greater than 10 percent) within 30 days prior to screening.
• Subject has an allergy to or has experienced side effects with opioid antagonists
• Subject is unable to respond to or recognize potential side effects of the study drug. This may include, but is not limited to, subjects with a mental illness or disorder.

Where it is running

• Celerion Inc. — Tempe, Arizona, United States

Full record on ClinicalTrials.gov

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