Phase IC Study of Safety and PK of SQ109 300mg Daily

NCT ID: NCT01358162

Last Updated: 2013-05-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-11-30
• Study Completion Date: 2011-04-30

Brief Summary

Healthy male and female volunteers will be given SQ109 300mg daily for 14 days to assess the safety and tolerability and pharmacokinetics.

Detailed Description

This is a Phase 1C randomized, placebo controlled, double-blinded, in-patient trial of a single oral dose of 300 mg of SQ109 given daily for 14 consecutive days to evaluate the safety, tolerability and pharmacokinetics of SQ109 in normal healthy male and female subjects 18-45 years of age.

Each subject will receive 300 mg of SQ109 or placebo.

Conditions

Tuberculosis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

SQ109

300 mg of SQ109, orally, given daily for 14 consecutive days

Group Type: EXPERIMENTAL

SQ109

Intervention Type: DRUG

A single oral dose of 300 mg of SQ109 given daily for 14 consecutive days.

Placebo

Placebo given orally, daily for 14 consecutive days

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Placebo given orally, daily for 14 consecutive days

Interventions

Placebo

Placebo given orally, daily for 14 consecutive days

Intervention Type: OTHER

SQ109

A single oral dose of 300 mg of SQ109 given daily for 14 consecutive days.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subject must be 18 to 45 years of age (inclusive).
• Subject must be a healthy male or female volunteer (i.e., hematology, coagulation, clinical chemistries and urinalysis tests must be within study-defined ranges (See Appendix B). Clinical tests must be performed within 28 days of receiving first dose of study drug.
• Body Mass Index (BMI) must be between 18 and 30 kg/m2 inclusive.
• Subject must be Tuberculin Skin Test/Purified Protein Derivative (TST/PPD) negative (within the previous 1 year) at Screening. The TST/PPD may be omitted if the subject presents written evidence of having a negative test during the previous 12 months.
• Subject must be able to give voluntary written informed consent before any study related procedure is performed.
• If female, has no childbearing potential or agrees to avoid becoming pregnant from the day of screening through their entire participation in the trial (Day 28) by using one of the following acceptable methods of birth control plus recommended use of a barrier method (condom) by the male partner (even if vasectomized):

1. intrauterine contraceptive device; or

2. diaphragm in combination with contraceptive jelly, cream, or foam; or

3. spermicide; or

4. abstinence. Non-childbearing potential is defined as being post-menopausal for at least 2 years, status after bilateral tubal ligation for at least 1 year, status after bilateral oophorectomy or status after hysterectomy.

Hormonal contraceptives of any type or form (including oral, transdermal, vaginal or depot preparations) will not be allowed during the study.

• All female subjects of childbearing potential must have a negative serum pregnancy test at screening and within 24 hours of the first dose of study product.
• Male subjects must agree to use an acceptable barrier method for birth control (abstinence or use of a condom with spermicide) from screening through Study Day 28 and advice and recommend use of additional birth control (as in criterion 6 above) to female sex partners throughout the study.
• Subject agrees not to donate blood during the study and up to 30 days after Study Day 28.
• Subject agrees to comply with all study requirements, including clinic house rules.

Exclusion Criteria

• A history of clinically significant gastrointestinal, renal, hepatic, neurologic, hematologic, endocrine, oncologic, pulmonary, immunologic, psychiatric, or cardiovascular disease or any other condition which, in the opinion of the Principal Investigator (PI), would jeopardize the safety of the subject or impact the validity of the study results.
• Subject has been on an abnormal diet during the 4 weeks preceding the study. Abnormal diet is defined as a diet in which the subject has a significant change in eating habits (e.g., liquid diet only) and an unbalanced diet (e.g., protein only, high fat, low carbohydrate, etc.).
• Subject has received an investigational drug in a clinical trial within 30 days prior to study initiation.
• Subject has used any OTC medication, including vitamins and herbal supplements, within 7 days prior to Day 1 of the study, unless in the opinion of the PI, the substance would not likely impact on the conduct of this study, including PK of SQ109.
• Subject has used any prescription medication within 14 days prior to Day 1 of the study, or the use of hormonal preparations containing sex hormones within 30 days prior to Day 1 of the study.
• Subject has any current medical condition requiring treatment with medication, either prescription or OTC.

Subject has been treated with any known CYP450 enzyme altering drugs such as azoles, antifungals, barbiturates, phenothiazines, cimetidine, carbamazepine, etc., within 30 days prior to Day 1 of the study.

• Subject has a positive blood screen for HIV, hepatitis B surface antigen (HBsAg), or hepatitis C antibody and/or a positive history for alcohol abuse or dependence and/or a positive serum ethanol or a positive urine screen for drugs of abuse (amphetamines, barbiturates, benzodiazepines, cocaine metabolites, marijuana, opiates, phencyclidine (PCP)).
• Subject has a baseline QTcF interval >450 msec (males) or >470 msec (females) (defined in Section 9.1.3) or a family history of prolonged QTcF syndrome or premature cardiac death.
• Subject has Wolf Parkinson White Syndrome (WPW) or family history of WPW or a history of supra-ventricular tachycardias or syncope.
• Subject has lived with a person having active TB or has traveled to an area of endemic TB within the past 12 months.
• Subject has an abnormal result on the Ishihara color test, the funduscopic exam, current optic neuritis or known retinal disease.
• Subject has an uncontrolled intercurrent illness (i.e., active infection) or fever (oral temperature >/=100 degrees F or >/= 37.7 degrees C).
• Subject has had major surgery within 4 weeks of study entry.
• Women who are pregnant or breastfeeding.
• Subject has donated blood within the past 30 days prior to Day 1 of the study.
• Subject has allergy to ethambutol or related compounds.
• Subject is an employee of or family member of an employee of Sequella, Quintiles, or DynPort Vaccine Company LLC (DVC).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Quintiles Phase I Services - Overland Park

Overland Park, Kansas, United States

Countries

United States

Other Identifiers

N01AI80024C

Identifier Type: -

Identifier Source: secondary_id

09-0111

Identifier Type: -

Identifier Source: org_study_id