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Study of the Effects of ITCA 650 on Gastric Emptying and Interaction of ITCA 650 on 4 Commonly Studied Drugs

2017年1月26日 更新者:Intarcia Therapeutics

A Phase 1, Fixed-Sequence, Open-label Study in Healthy Subjects to Estimate the Effects of ITCA 650 on Gastric Emptying and on the Absorption Pharmacokinetics of Each of 4 Commonly Studied Drug/Drug Interaction (DDI) Probe Compounds

A Phase 1, Fixed-Sequence, Open-label Study in Healthy Subjects to Estimate the Effects of ITCA 650 on Gastric Emptying and on the Absorption Pharmacokinetics of Each of 4 Commonly Studied DDI Probe Compounds.

研究概览

详细说明

Acetaminophen will be use to assess the effect of ITCA 650 on the rate of gastric emptying.

Interactions between ITCA 650 and the medications lisinopril, digoxin, atorvastatin, and warfarin will also be studied.

研究类型

介入性

注册 (实际的)

33

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

    • Kansas
      • Overland Park、Kansas、美国、66211
        • Quintiles

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 65年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Body mass index (BMI) between 19 to 32 kg/m2.
  • Glycosylated hemoglobin A1c (HbA1c )<6.5%.
  • Normal renal function (eGFR ≥80 mL/min/1.73 m2).
  • Women of child bearing potential - use of an additional adequate method of contraception during the study and until 1 additional menstrual cycle following the end-of-study (EOS) visit. Adequate methods of contraception for women of child bearing potential (WOCBP) include: mechanical products (ie, intrauterine device [IUD]-copper IUD); or barrier methods (eg, diaphragm, condoms, cervical cap) with spermicide.

Exclusion Criteria:

  • History of type 1 or type 2 diabetes.
  • History or evidence of myocardial infarction, coronary revascularization (coronary artery bypass grafting or percutaneous coronary intervention), unstable angina, or cerebrovascular accident or stroke.
  • History of uncontrolled hypertension.
  • History or evidence of acute or chronic pancreatitis.
  • History of liver disease.
  • History of medullary thyroid cancer or a personal or family history of multiple endocrine neoplasia type 2.
  • Poor thyroid, liver, or renal function.
  • Weight loss surgery or requires weight loss medications.
  • History of malignancy (not including basal or squamous cell carcinoma of the skin with past 5 years). (Subjects who have been disease free for 5 years may be included.)
  • History of active alcohol or substance abuse.
  • Weekly consumption of more than 7 alcoholic beverages for females and 14 alcoholic beverages for males.
  • Excessive in xanthine consumption (more than 5 cups of coffee or equivalent per day).
  • Treatment with medications that affect GI motility.
  • Any condition that would affect drug transit time or absorption (eg, gastrointestinal bypass surgery, partial or total gastrectomy, small bowel resection, chronic diarrhea, vagotomy, chronic gastroesophageal reflux disease, malabsorption, colostomy, Crohn's disease, ulcerative colitis, or celiac sprue).
  • History of hypersensitivity to exenatide.
  • Contraindications or warnings according to the specific label(s) for acetaminophen, atorvastatin, lisinopril, digoxin or warfarin therapy.
  • Women that are pregnant, lactating, or planning to become pregnant.
  • Concurrent use of anticoagulants, including daily low dose aspirin (81 mg).
  • History of or positive results on screening tests for hepatitis B and/or hepatitis C and/or human immunodeficiency virus (HIV).
  • Planned in-patient surgery, dental procedure, or hospitalization during the study.
  • Prior or current treatment with any glucagon-like peptide-1 (GLP-1) receptor agonist (eg, Bydureon™, Byetta®, Victoza®, Tanzeum® or exogenous native GLP-1) or prior participation in an ITCA 650 clinical trial.
  • Use or intended use of any drug or other product that inhibits or induces cytochrome P450 (CYP)1A2, CYP2C9, CYP2C19, or CYP3A4 within 14 days prior to the first dose of warfarin or ITCA650 or during the conduct of the study.
  • History of thrombophlebitis, thromboembolic disorders, or deep vein thrombophlebitis.
  • Fasting triglycerides above upper limit of normal at Screening.
  • Any gastrointestinal complaints within 7 days prior to first dosing.
  • Taking drugs or natural herbal supplements (such as albuterol, antacids, and St. John's Wort) with known interactions with atorvastatin, lisinopril, digoxin, or warfarin from within 7 days prior to Day 1 until EOS
  • Consumed or unwilling to refrain from grapefruit, cranberries, grapefruit- or cranberry-containing products, or Seville oranges from within 7 days prior to Day 1 until EOS.
  • Chronic use of analgesics, pain medication, or non-steroidal anti-inflammatory agents.

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:其他
  • 分配:不适用
  • 介入模型:单组作业
  • 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:Experimental Treatment
ITCA 650 20/60 mcg/day Acetaminophen 1000 mg Atorvastatin 40 mg Lisinopril 20 mg Warfarin 25 mg Digoxin 0.5 mg
ITCA 650 osmotic mini pump delivering exenatide 20 mcg/day for 14 days, followed by ITCA 650 osmotic mini pump delivering exenatide 60 mcg/day.
Oral acetaminophen 1000 mg on Day 1 and Day 27
Oral atorvastatin 40 mg on Day 2 and Day 28
Oral lisinopril 20 mg on Day 2 and Day 28
Oral warfarin 25 mg on Day 2 and Day 28
Oral digoxin 0.5 mg on Day 2 and Day 28

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Area under the concentration-time curve from time zero to the last measurable concentration [AUC(0-last)]) of acetaminophen alone and in the presence of ITCA 650.
大体时间:time zero to 10 weeks
time zero to 10 weeks
Maximum plasma concentration ([Cmax]) of acetaminophen alone and in the presence of ITCA 650
大体时间:time zero to 10 weeks
time zero to 10 weeks
Area under the concentration-time curve (AUC(0-last)) of atorvastatin, lisinopril, digoxin, R-warfarin, and S-warfarin each alone and in the presence of ITCA 650.
大体时间:time zero to 10 weeks
time zero to 10 weeks
Cmax of atorvastatin, lisinopril, digoxin, R-warfarin, and S-warfarin each alone and in the presence of ITCA 650.
大体时间:time zero to 10 weeks
time zero to 10 weeks

次要结果测量

结果测量
大体时间
Time to maximum plasma concentration (tmax) of acetaminophen
大体时间:time zero to 10 weeks
time zero to 10 weeks
tmax of atorvastatin, lisinopril, digoxin, R warfarin, and S-warfarin
大体时间:time zero to 10 weeks
time zero to 10 weeks
AUC(0-last) of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
大体时间:time zero to 10 weeks
time zero to 10 weeks
Cmax of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
大体时间:time zero to 10 weeks
time zero to 10 weeks
Maximum effect (Emax)from time zero to the last measurable concentration (AUEC(0-last)) of international normalized ratio (INR) of warfarin.
大体时间:time zero to 10 weeks
time zero to 10 weeks
Cmax of ITCA 650, 20 mcg/d and 60 mcg/d
大体时间:within 8 hours after placement of ITCA 650
within 8 hours after placement of ITCA 650
Treatment-emergent adverse events (TEAEs) including any events local to the placement site, clinical laboratory measurements, ECGs, vital signs and physical examinations.
大体时间:time zero to 10 weeks
time zero to 10 weeks
Tmax of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
大体时间:time zero to 10 weeks
time zero to 10 weeks
Cmin of ITCA 650, 20 mcg/d and 60 mcg/d
大体时间:time zero to 10 weeks
time zero to 10 weeks
Tmax of ITCA 650, 20 mcg/d and 60 mcg/d
大体时间:time zero to 10 weeks
time zero to 10 weeks
Tmin of ITCA 650, 20 mcg/d and 60 mcg/d
大体时间:zero to 10 weeks
zero to 10 weeks
Time of maximum effect (tEmax)from time zero to the last measurable concentration (AUEC(0-last)) of international normalized ratio (INR) of warfarin.
大体时间:zero to 10 weeks
zero to 10 weeks
Area under the effect-time curve from time zero to the last measurable concentration (AUEC(0-last)) of international normalized ratio (INR) of warfarin.
大体时间:zero to 10 weeks
zero to 10 weeks

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

学习开始

2015年12月1日

初级完成 (实际的)

2016年3月1日

研究完成 (实际的)

2016年3月1日

研究注册日期

首次提交

2015年12月21日

首先提交符合 QC 标准的

2015年12月24日

首次发布 (估计)

2015年12月30日

研究记录更新

最后更新发布 (估计)

2017年1月27日

上次提交的符合 QC 标准的更新

2017年1月26日

最后验证

2017年1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.

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