此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Effects of SQ109 on QTc Interval in Healthy Subjects

Phase 1 Crossover Study to Assess the Effects of SQ109 on QTc Interval in Healthy Subjects

This will be a single center, open label, crossover study to evaluate the safety and tolerability of multiple dose levels of SQ109.

研究概览

详细说明

This is a Phase 1, randomized, single-center, clinical study of SQ109 to evaluate the potential for this drug to produce QTc prolongation. The study population is healthy male and female subjects, aged 18-45 years. Pharmacokinetics of SQ109 will be measured using interval plasma samples.The overall study design will incorporate within it a four-period investigation suitable for the QT evaluation of an active study treatment. The primary goal of the sample size considerations will be to ensure that the sample size employed during this phase of the study will be adequate to ensure a high likelihood of a successful demonstration of the QT safety of 300 and 450 mg/day SQ109. All subjects will be randomized to a sequence of three seven-day dosing periods, with each dosing period occurring once per subject. The final seven-day dosing period will occur after the first sequence of three dosing periods is completed. A washout period of at least seven days will occur between all dosing periods, and a follow-up visit will occur.

研究类型

介入性

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Ohio
      • Cleveland、Ohio、美国、44106-1716
        • Case Western Reserve University - Case Medical Center - Infectious Disease & HIV Medicine

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 45年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Men and women aged 18 to 45 years, inclusive.
  • Ability to understand the consent process and procedures.
  • Informed consent obtained and signed.
  • Comprehension of the study objectives and procedures which will be determined by the recruiter using a series of questions after explaining the procedures.
  • Subject agrees to be available for all study visits and is able to comply with protocol requirements for the entire duration of the study.
  • Subject agrees not to participate in another clinical trial at any time during the study period.
  • Subjects who have a body mass index (BMI) >/=18 kg/m^2 and </= 35 kg/m^2
  • General good health, without current medical illness or clinically significant abnormal physical examination findings that classify the subject as other than healthy as determined by study investigators
  • Negative serum pregnancy test at screening and a negative urine pregnancy test on the day of admittance to the inpatient phase for all female subjects of child bearing potential.
  • Negative urine toxicity screen for alcohol, marijuana, cocaine metabolite, amphetamines, opiates, PCP, barbiturates, and benzodiazepines.
  • Agreement by subjects with reproductive potential to use an adequate method of contraception during the study and for 90 days after study drug administration. Female subjects must agree to the use of two reliable methods of contraception while receiving study drug and for 90 days after study drug administration, which can include: condoms, spermicidal gel, diaphragm, hormonal or non-hormonal intrauterine device, surgical sterilization, oral contraceptive pill, and depot progesterone injections. If a male subject is heterosexually active, the subject and his partner must use at least two forms of the listed contraceptive methods.

Exclusion Criteria:

Subjects meeting any exclusion criteria at baseline will be excluded from study partcipation.

Note that individuals with a history of cardiac arrhythmias will not be included as subjects in this study.

  • Medical condition that precludes participation, including the following:

    • Hypertension with confirmed systolic blood pressure >140 mmHg or confirmed diastolic blood pressure >90 mmHg, measured after 10 - 15 minutes of rest.
    • Morbid obesity (BMI>35)
    • Current diagnosis of pulmonary disease including latent TB
    • Current diagnosis of asthma, which has required use of asthma medications within the past year
    • History of or current diagnosis of diabetes
    • Autoimmune disorder, such as lupus, Wegener's, rheumatoid arthritis
    • History of malignancy except low-grade skin cancer, (i.e., basal cell carcinoma thought to be cured)
    • Chronic renal, hepatic, or pulmonary disease condition that could interfere with the absorption of the study drug (e.g., surgical resection of significant proportions of the stomach or bowel, gastric bypass, gastric banding, irritable bowel syndrome, inflammatory bowel disease)
    • History of known Clostridium difficile infection
    • Blood donation within the previous 6 weeks
    • History of cardiac rhythm abnormality including Wolff/Parkinson/White syndrome
    • History of prolonged QT interval
    • History of allergy or photosensitivity to fluoroquinolones
  • Prolongation of QTcF interval (i.e., confirmed QTcF interval of 450 milliseconds or greater)
  • Clinically significant abnormal 12 lead electrocardiogram at screening in the judgment of the investigator, or based on the formal ECG reading; history of any cardiac abnormalities, including conduction abnormalities such as Wolff-Parkinson-White, dysrhythmias, or coronary artery disease
  • Laboratory abnormalities at Screening outside of the ranges given below. Note, if one or more screening laboratory values are outside the acceptable range on the initial screen, the abnormal test(s) may be repeated once from a single blood draw:

    • Serum creatinine (<1.1 x ULN),
    • Hemoglobin (11.0-17.5g/dL),
  • Platelet count (125,000-450,000mm^3),

    • Absolute neutrophil count (>1300 mm^3),
    • Aspartate aminotransferase (AST, </=1.2 x ULN),
    • Alanine aminotransferase (ALT, </=1.2 x ULN),
    • Proteinuria greater than trace (spot urine) and/or hematuria greater than trace.
  • Positive serology results for HIV, HBsAg, or HCV antibodies
  • Positive urine drug screen for cannabinoids, cocaine, amphetamines, opiates, benzodiazepine, barbiturates, and/or PCP.
  • Febrile illness with temperature documented >38 degrees C within 7 days of dosing.
  • Pregnancy or breastfeeding
  • Known allergic reactions to study drug components, including ingredients present in the formulation.
  • Treatment with another investigational drug within 30 days of dosing.
  • Lack of ability to fully understand the informed consent. This will be determined by the recruiter/interviewer after explaining the consent and observing the subject reading the consent.
  • Ingestion of prescription medications, over-the-counter medicines, grapefruit juice, or specific supplements in the week prior to study enrollment and during the course of the study that, in the judgment of the PI could affect the metabolism of the study drug or safety of the participant (see Concomitant Medications, Section 6.6).
  • Use of any form of tobacco, including cigarette smoking, pipe smoking, or oral tobacco; if a former smoker or tobacco user, the subject must not have used tobacco for 30 days before screening.
  • Any specific condition that, in the judgment of the Investigator, precludes participation because it could affect subject safety.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:SQ109 450 mg
Single daily dose of oral 450mg SQ109 for 7 days.
300mg or 450mg of SQ109 administered orally, once daily for 7 days.
有源比较器:Moxifloxacin
Single daily dose of oral 400mg moxifloxacin for 7 days followed by 7 days washout period.
400mg of moxifloxacin (positive control) administered orally, once daily for 7 days.
安慰剂比较:SQ109 Placebo
Single daily dose of oral SQ109 placebo for 7 days followed by 7 days washout period.
Placebo is a round, coated, yellow, unscored tablet. SQ109 Placebo administered orally, once daily for 7 days.
实验性的:SQ109 300 mg
Single daily dose of oral 300mg SQ109 for 7 days followed by 7 days washout period.
300mg or 450mg of SQ109 administered orally, once daily for 7 days.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Solicited and unsolicited adverse events, including symptoms, physical findings, laboratory testing, holter monitor and ECG changes for 300mg/day SQ109
大体时间:Days 1-7 of each dosing period and 30 days after last dosing period.
Days 1-7 of each dosing period and 30 days after last dosing period.
Electrocardiogram and holter monitor data (QTc, T wave forms, QRS, RR and PR intervals) for 300mg/day SQ109
大体时间:Days 1-7 of each dosing period and 30 days after last dosing period.
Days 1-7 of each dosing period and 30 days after last dosing period.

次要结果测量

结果测量
大体时间
Solicited and unsolicited adverse events, including symptoms, physical findings, laboratory testing, holter monitor and ECG changes for 450mg/day SQ109
大体时间:Days 1-7 of each dosing period and 30 days after last dosing period.
Days 1-7 of each dosing period and 30 days after last dosing period.
Pharmacokinetics of SQ109 at doses of 300 or 450mg/day; AUC0-, (Cmax), time to maximum concentration (Tmax), elimination rate constant, elimination half-life, clearance, volume of distribution, and urinary excretion
大体时间:Day 1 and Day 6 of each dosing period
Day 1 and Day 6 of each dosing period
Electrocardiogram and holter monitor data (QTc, T wave forms, QRS, RR and PR intervals) for 450mg/day SQ109
大体时间:Days 1-7 of each dosing period and 30 days after last dosing period.
Days 1-7 of each dosing period and 30 days after last dosing period.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

初级完成 (预期的)

2015年12月1日

研究完成 (预期的)

2015年12月1日

研究注册日期

首次提交

2013年5月23日

首先提交符合 QC 标准的

2013年6月6日

首次发布 (估计)

2013年6月11日

研究记录更新

最后更新发布 (估计)

2014年3月24日

上次提交的符合 QC 标准的更新

2014年3月20日

最后验证

2013年5月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅