The purpose of this study is to evaluate the drug-drug interaction potential of
clarithromycin XL on Diltiazem hydrochloride (DTZ) 2% cream.
Inclusion Criteria:
1. Were healthy subjects (as confirmed by medical history, laboratory work, and physical
exam);
2. Were between 18 and 60 years of age, inclusive;
3. If of childbearing potential, were using an acceptable form of birth control (ie,
nonhormonal intra-uterine device, diaphragm, condom, bilateral tubal ligation,
abstinence, or were in a monogamous relationship with a partner who had a vasectomy);
4. In the case of females of childbearing potential, had a negative serum pregnancy test
(SPT) at Screening and a negative urine pregnancy test (UPT) at Study Day - 1, (a
woman was considered to be of childbearing potential unless she was postmenopausal
for at least 12 months or was surgically sterile [hysterectomy, bilateral
oophorectomy]);
5. Had clinical lab tests (hematology, chemistry, and urinalysis), an electrocardiogram
(ECG), and vital signs within normal limits, or assessed by the investigator as not
of clinical significance; and
6. Were able to read, understand, and provide signed informed consent.
Exclusion Criteria:
1. On any drug treatment at the time of the study;
2. Had donated plasma (500 mL) within 7 days prior to drug administration;
3. Had donated or lost whole blood (excluding the volume of blood that was to be drawn
during the screening procedures of this study) prior to administration of the study
medication as follows: 50 mL to 499 mL of whole blood within 30 days, or more than
499 mL of whole blood within 56 days prior to drug administration;
4. Were using and were unwilling to stop any other concomitant topical preparations in
or around the anus and perianal area from Day −1 through the end of the study;
5. Had a hypersensitivity or allergy to the investigational compound/compound class used
in this study, and bacterial fighting medications, including but not limited to
clarithromycin XL , azithromycin, telithromycin, and erythromycin or to calcium
channel blockers;
6. Had a history or presence of neurological, endocrinal, cardiovascular, pulmonary,
hematologic, immunologic, psychiatric, or metabolic disease, that, in the opinion of
the investigator, could have interfered with the study conduct or observation;
7. Were unable to adhere to or understand the requirements of the protocol;
8. Had a body mass index > 40 kg/m2;
9. Had a screening ECG >470 QTCF for females and >450 QTCF for males;
10. Were on active treatment with anti-viral therapies (eg, indinavir, nelfinavir,
ritonavir) for human immunodeficiency virus (HIV);
11. Had been treated with any of the following medications within 14 days prior to
signing the ICF:
- CYP450 inhibitors and inducers;
- CYP3A4 substrates, inhibitors, and inducers;
- Benzodiazepines;
- β-adrenoceptor antagonists (beta-blockers);
- Calcium channel blockers;
- Digoxin;
- Investigational agents;
- Opioids.
12. Had any of the following concomitant disease states:
- Sick sinus syndrome except in the presence of a functioning ventricular
pacemaker;
- Second-or third-degree atrioventricular block except in the presence of a
functioning ventricular pacemaker;
- Hypotension (< 90 mm Hg systolic);
- Acute myocardial infarction and pulmonary congestion documented by x-ray;
- History of clinically significant renal disease;
- History of clinically significant Alzheimer's or Parkinson's disease;
- History of clinically significant hepatic disease;
- Current infection treated with a macrolide antibiotic;
- Clinical evidence or history of fecal incontinence;
- Clinical evidence or history of anal fistula;
- Clinical evidence or history of anal abscess;
- History of inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis);
- History of any prior anal or rectal surgery including but not limited to:
lateral sphincterotomy and anal stretch;
13. Had a major organ transplant;
14. Had a serious illness in the 4 weeks preceding the beginning of treatment (ie, that
resulted in missed work or hospitalization);
15. Had received treatment for any type of internal cancer within the 5 years prior to
enrollment;
16. Had, in the opinion of the investigator, clinically significant abnormal clinical
laboratory results at the time of screening;
17. Were females who were pregnant, were planning to become pregnant during the study, or
were breastfeeding a child;
18. Were currently using narcotics chronically;
19. Were currently a smoker;
20. Had used an investigational drug or had participated in an investigational study
within 30 days prior to dosing;
21. Had used prescription medication within 14 days prior to administration of study
medication or over-the-counter (OTC) products (including natural food supplements
vitamins, garlic as a supplement) within 7 days prior to administration of study
medication, except for topical products without systemic absorption;
22. Were an employee, family member, or student of the investigator or clinical site;
23. Had any food allergy, intolerance, restriction, or special diet that, in the opinion
of the investigator, could have contraindicated the subject's participation in this
study.
