Overview

Safety, Tolerability, and Pharmacokinetics of Single, Escalating Oral Doses of RTI-336 in Healthy, Male Subjects

Status:
Completed
Trial end date:
2009-03-01
Target enrollment:
0
Participant gender:
Male
Summary
This is the first study to be conducted in humans for RTI-336, a new chemical entity, with evaluations focusing on the safety, tolerability, and pharmacokinetics of RTI-336 following administration of single, oral doses. RTI-336 is a novel dopamine transporter inhibitor of the 3-phenyltropane class, and is currently being developed by RTI International as a potential pharmacotherapy to treat cocaine dependence. Data from this study will be used to plan and define dose ranges for subsequent studies.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
RTI International
Collaborator:
National Institute on Drug Abuse (NIDA)
Criteria
Inclusion Criteria:

A subject will be eligible for inclusion in this study only if all of the following
criteria are met:

1. Subject provides signed and dated, written informed consent prior to any
study-specific procedures being performed, including washout of any medications and
compliance with food/beverage restrictions.

2. Subject is a healthy adult male, 18-50 years of age, inclusive, at the time of
consent, with body weight greater than or equal to 50 kg and a body mass index (BMI)
in the range of 18-30 kg/m2, where BMI = weight (kg)/[height (m)]2.

3. Subject has a negative pre-study urine drug screen and no history of cocaine use or
use of other illicit drugs or substances of abuse within 12 months of the screening
visit. Drugs or substances analyzed in the urine screen include cocaine, amphetamines,
barbiturates, opioids, cannabinoids, benzodiazepines, phencyclidine, alcohol, and
cotinine.

4. Subject is a non-tobacco user or a prior user who quit using tobacco at least 90 days
prior to screening.

5. Subject has no history of any cardiovascular disease and has a normal ECG and serum
troponin at screening.

6. Subject is negative for hepatitis C antibodies, hepatitis B surface antigen and human
immunodeficiency virus (HIV) at screening.

7. Subject is in good general health, in the opinion of the Investigator, and as
determined by medical history, physical examination, vital signs, 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 for
sodium, protein, total WBC, hematocrit, hemoglobin, reticulocyte count, platelets, AST
(SGOT), ALT (SGPT), GGT, and troponin I. Within upper limit of normal and no more than
10% below lower limit: BUN creatinine, bilirubin, total alkaline phosphatase, creatine
kinase, and LDH. Within 10% of normal range and considered to be not clinically
significant:calcium chloride, phosphorus, albumin, globulin, cholesterol,
triglycerides, and RBC. No clinically significant abnormalities: glucose, potassium,
white blood cell differential, red blood cell indices, uric acid, and urinalysis.

8. Subject is willing to use barrier contraception with spermicide during sexual
intercourse while enrolled in this study and for at least 30 days after the last dose
of study drug.

9. 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.

10. Subjects is fluent in either English or Spanish

Exclusion Criteria:

A subject will be excluded from participation in the study if any of the following criteria
applies:

1. Subject self-reports a history of chronic illicit drug use or chronic use of other
substances of abuse.

2. Subject has a positive urine drug/alcohol/cotinine test at screening or prior to
dosing in any dose period.

3. Subject has a history or evidence of hepatic, gastrointestinal, renal, respiratory,
ophthalmic, cardiovascular, hematologic, endocrine/metabolic, neurologic, immunologic,
oncologic or psychiatric illness or significant abnormalities.

4. Subject has a history of and/or current major depression, psychotic symptoms, or
anxiety disorder(s) based on the Major Depressive Episode, Psychotic, and Anxiety
Disorder modules of the Structured Clinical Interview for DSM Disorders (details
documented in study protocol).

5. Subject has a family history of psychiatric illness (psychosis, depression, anxiety
disorders).

6. Subject has an abnormal ECG at screening or prior to dosing in each dose period.
Premature atrial contraction or premature ventricular contraction is considered
abnormal, as are bundle branch blocks, second or third degree heart block, or any
arrhythmia other than respiratory sinus arrhythmia. Abnormalities also include but are
not limited to the following: Heart Rate < 45 or > 100 bpm; PR interval < 120 or > 220
msec; QRS duration < 70 or > 120 msec; and QTC interval (Bazett) > 460 msec.

7. Subject has a history or family history of QT prolongation, arrhythmia, or
uncontrolled hypertension.

8. Subject has a history of seizure, head injury, neurosurgery or brain trauma, or a
family history of non-traumatic seizure.

9. Subject is positive for hepatitis C antibodies at screening, or hepatitis B surface
antigen or HIV at screening.

10. Subject has an infection of any type or clinically significant abnormality identified
by the screening medical or laboratory evaluations.

11. Subject has a history of using tobacco-containing products within 90 days of
screening.

12. 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 a half-pint (220 mL) of beer, or 1 measure of spirits, or 1
glass (125 mL) of wine.

13. Subject has consumed grapefruit or grapefruit-containing, or poppy-seed or
quinine-containing substances within 14 days of the first dose period.

14. Subject has used any other drug, including prescription or non-prescription
medications and herbal supplements, within 30 days prior to the first dose of study
drug, with the exception of acetaminophen, which may be taken up to 24 hours prior to
dosing in each dose period.

15. Subject has a history or presence of gastrointestinal, hepatic or renal disease, or
other condition/surgical intervention known to interfere with the absorption,
distribution, metabolism, or excretion of drugs.

16. Subject has had any acute gastrointestinal illness or infection within 2 weeks prior
to first dose of study drug.

17. Subject has participated in an investigational trial within 45 days prior to the first
dose of study drug.

18. Subject is unable to donate blood, has a clotting disorder(s), or has donated/lost
>500 mL blood within 8 weeks prior to screening.

19. Subject has an unexplained weight loss or gain >10% within 30 days prior to screening.

20. Subject has an allergy to 3-phenyltropane analogs (e.g., brasofensine, tesofensine),
heparin, haloperidol, dopamine agonists, or related compounds.

21. 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.

22. Subject has any condition or set of circumstances not otherwise excluded which in the
judgment of the Investigator could interfere with the subject's ability to comply with
the protocol requirements and restrictions and completion of study evaluations, or
could pose safety risks to the subject.

23. Subject has performed strenuous exercise within 48 hours prior to the screening
examination or refuses to abstain from strenuous exercise for 48 hours prior to and 48
hours after each dose period, 48 hours prior to the day 8 visit, or 48 hours prior to
the follow-up visit.

24. Subject has a screening serum troponin result above the clinical laboratory's normal
range.