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Study to Determine the Single and Repeat Dose Pharmacokinetics, Food Effect, Proton Pump Inhibitor (PPI) Drug Interaction, Safety and Tolerability of Oral Prototype Formulations of BOS172767 in Healthy Subjects

2020年11月17日 更新者:Boston Pharmaceuticals

A Phase 1 Study to Determine the Single and Repeat Dose Pharmacokinetics, Food Effect, PPI Drug Interaction, Safety and Tolerability of Oral Prototype Formulations of BOS172767 in Healthy Subjects

Part 1 of the study will be conducted to provide additional information on the safety and tolerability of single doses of BOS172767 in healthy participants, to evaluate the pharmacokinetic (PK) profiles (including relative bioavailability) of BOS172767 following oral administration of 3 prototype formulations in healthy participants compared to an immediate release capsule formulation (reference), and also to determine the relative bioavailability of a selected BOS172767 prototype formulation in the fed and fasted states.

Part 2 of the study will be conducted to provide additional information on the safety and tolerability of escalating single doses of the selected formulation of BOS172767 in healthy participants, to evaluate the PK profile following increased single doses of the selected formulation of BOS172767 following administration in healthy participants, and also to evaluate the dose linearity of the selected prototype.

Part 3 of the study will be conducted to provide additional information on the safety, tolerability, and PK of the selected formulation of BOS172767 following multiple ascending doses (MADs) over 14 days of dosing in healthy participants.

研究概览

详细说明

Part 1 is comprised of a single-dose, part-randomized, open-label, 6-way crossover in 12 healthy participants. Participants will be dosed on 6 separate occasions (in 6 treatment periods), and will receive a single prototype of BOS172767 in each treatment period.

Part 2 is comprised of a single ascending dose, fixed-sequence, open-label, 3-way crossover with an optional fourth dosing period in 10 healthy participants. Participants will be dosed on 4 separate occasions (in 4 treatment periods), and will receive a single prototype of BOS172767 in each treatment period.

Part 3 is a double-blind (sponsor-open), placebo-controlled, randomized MAD part in 36 healthy participants (12 per study cohort). Participants will be dosed on 3 separate occasions (in 3 treatment periods), and will receive a single prototype of BOS172767 in each treatment period.

Parts 2 and 3 are contingent upon successful completion of Part 1.

研究类型

介入性

注册 (实际的)

28

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

      • Nottingham、英国
        • Quotient Sciences

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 50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:

  • Healthy males or healthy females of non-child bearing potential
  • Age 18 to 50 years of age at time of signing informed consent
  • Body mass index of 18.0 to 32.0 kilograms per meters squared (kg/m^2) at Screening, or, if outside the range, considered not clinically significant by the investigator
  • Must be willing and able to communicate and participate in the whole study
  • Must have a negative Quantiferon tuberculosis test at Screening
  • Must provide written informed consent
  • Must agree to use an adequate method of contraception

Exclusion Criteria:

  • Participants who have received any investigational medicinal product (IMP) in a clinical research study within the previous 3 months prior to dosing
  • Participants who are study site employees, or immediate family members of a study site or sponsor employee
  • Participants who have previously been enrolled (dosed) in this study
  • History of any drug or alcohol abuse in the past 2 years prior to Screening
  • Regular alcohol consumption in males >21 units per week and females >14 units per week (1 unit = ½ pint beer, 25 milliliters [mL] of 40% spirit or a 125 mL glass of wine)
  • Current smokers and those who have smoked within the last 12 months prior to Screening. A breath carbon monoxide reading of greater than 20 parts per million at Screening or admission
  • Current users of e-cigarettes and nicotine replacement products and those who have used these products within the last 12 months prior to Screening
  • Females of childbearing potential
  • Participants who do not have suitable veins for multiple venepunctures/cannulation as assessed by the investigator at Screening
  • Clinically significant abnormal biochemistry, haematology or urinalysis as judged by the investigator
  • Confirmed positive drugs of abuse test result
  • Positive hepatitis B surface antigen, hepatitis C virus antibody or human immunodeficiency virus results
  • Evidence of renal impairment at Screening, as indicated by an estimated creatinine clearance of <70 mL/minute using the Cockcroft-Gault equation
  • History of clinically significant cardiovascular, renal, hepatic, chronic respiratory or gastrointestinal disease (including gall stones and/or cholecystectomy), neurological or psychiatric disorder, as judged by the investigator
  • Serious adverse reaction or serious hypersensitivity to any drug or the IMP formulation excipients
  • Adverse reaction to rabeprazole, its excipients or any proton pump inhibitors (Part 2 only)
  • Presence or history of clinically significant allergy requiring treatment, as judged by the investigator. Hay fever is allowed unless it is active.
  • Donation or loss of greater than 400 mL of blood within the previous 3 months
  • Participants who are taking, or have taken, any prescribed or over-the-counter drug (other than 4 grams per day paracetamol or hormone replacement therapy) or herbal remedies in the 14 days before IMP administration. Exceptions may apply on a case by case basis, if considered not to interfere with the objectives of the study, as agreed by the Principal Investigator and sponsor's medical monitor.
  • Participants who have any ongoing fungal infections (stable toe nail onychomycosis is allowed)
  • Failure to satisfy the investigator of fitness to participate for any other reason

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:基础科学
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Part 1: Regimen A
Participants will be treated with a BOS172767 200 milligram (mg) spray dried dispersion tablet (2 × 100 mg tablets) in the fasted state on Day 1.
Oral tablets
实验性的:Part 1: Regimen B
Participants will be treated with a BOS172767 200 mg lipid capsule (2 × 100 mg capsules) in the fasted state on Day 1.
Oral capsules
实验性的:Part 1: Regimen C
Participants will be treated with a BOS172767 200 mg micronized capsule (2 × 100 mg capsules) in the fasted state on Day 1.
Oral capsules
实验性的:Part 1: Regimen D
Participants will be treated with a BOS172767 200 mg immediate release reference capsule formulation (2 × 100 mg capsules) in the fasted state on Day 1.
Oral capsules
实验性的:Part 1: Regimen E
Participants will be treated with a selected dose of a prototype formulation of BOS172767 in the fasted state on Day 1.
Oral tablets
Oral capsules
Oral capsules
Oral capsules
实验性的:Part 1: Regimen F
Participants will be treated with a selected dose of a prototype formulation of BOS172767 in the fed state on Day 1.
Oral tablets
Oral capsules
Oral capsules
Oral capsules
实验性的:Part 2: Regimen G
Participants will be treated with 400 mg of the selected BOS172767 prototype in the fasted state on Day 1.
Oral tablets
Oral capsules
Oral capsules
Oral capsules
实验性的:Part 2: Regimen H
Participants will be treated with 600 mg of the selected BOS172767 prototype in the fasted state on Day 1.
Oral tablets
Oral capsules
Oral capsules
Oral capsules
实验性的:Part 2: Regimen I
Participants will be treated with 800 mg of the selected BOS172767 prototype in the fasted state on Day 1.
Oral tablets
Oral capsules
Oral capsules
Oral capsules
实验性的:Part 2: Regimen J
Participants will be treated with rabeprazole on Days -3 to -1, and a selected dose of the BOS172767 prototype in the fasted state on Day 1.
Oral tablets
Oral capsules
Oral capsules
Oral capsules
口服片剂
实验性的:Part 3: Regimen K
Participants will be treated with 400 mg of a BOS172767 prototype or matching placebo once daily (QD) or twice daily (BID) for 14 days (Days 1 to 14).
Oral tablets
Oral capsules
Oral capsules
Oral capsules
Oral capsules
Oral tablets
实验性的:Part 3: Regimen L
Participants will be treated with 600 mg of a BOS172767 prototype or matching placebo QD or BID for 14 days (Days 1 to 14).
Oral tablets
Oral capsules
Oral capsules
Oral capsules
Oral capsules
Oral tablets
实验性的:Part 3: Regimen M
Participants will be treated with 800 mg of a BOS172767 prototype or matching placebo QD or BID for 14 days (Days 1 to 14).
Oral tablets
Oral capsules
Oral capsules
Oral capsules
Oral capsules
Oral tablets

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Parts 1, 2, and 3: Number of participants with any treatment-emergent serious adverse event (TESAE)
大体时间:up to 33 weeks
up to 33 weeks
Parts 1, 2, and 3: Number of participants with any treatment-emergent non-serious adverse event (TEAE)
大体时间:up to 33 weeks
up to 33 weeks
Parts 1, 2, and 3: Number of participants with abnormal, clinically significant physical examination findings
大体时间:up to 33 weeks
up to 33 weeks
Parts 1, 2, and 3: Number of participants with abnormal, clinically significant safety laboratory test findings
大体时间:up to 33 weeks
up to 33 weeks
Parts 1, 2, and 3: Number of participants with abnormal, clinically significant vital sign values
大体时间:up to 33 weeks
up to 33 weeks
Parts 1, 2, and 3: Number of participants with abnormal, clinically significant electrocardiogram findings
大体时间:up to 33 weeks
up to 33 weeks
Parts 1 and 2: Plasma concentration of BOS172722
大体时间:predose; 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16 hours postdose (Day 1); 24 and 36 hours postdose (Day 2); 48 hours postdose (Day 3)
predose; 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16 hours postdose (Day 1); 24 and 36 hours postdose (Day 2); 48 hours postdose (Day 3)
Part 2 (Regimen I): Plasma concentration of BOS172722
大体时间:admission to pre-dose (admission to dosing), 0 to 6 (Day 1), 6 to 12 (Day 1), 12 to 24 (Day 1), and 24 to 48 (Days 2 to 3) hours postdose
admission to pre-dose (admission to dosing), 0 to 6 (Day 1), 6 to 12 (Day 1), 12 to 24 (Day 1), and 24 to 48 (Days 2 to 3) hours postdose
Part 3: Plasma concentration of BOS172722
大体时间:Days 1 and 7: pre-dose; 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, and 24 hours postdose. Days 4, 6, 9, 11, and 12: pre-dose. Day 14: pre-dose; 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, 24, 48, 72, 96, and 120 hours post-final dose
Days 1 and 7: pre-dose; 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, and 24 hours postdose. Days 4, 6, 9, 11, and 12: pre-dose. Day 14: pre-dose; 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, 24, 48, 72, 96, and 120 hours post-final dose
Part 3 (Regimen M): Plasma concentration of BOS172722
大体时间:admission to pre-dose on Day 1; 0 to 6, 6 to 12, and 12 to 24 hours postdose on Days 1, 7, and 14
admission to pre-dose on Day 1; 0 to 6, 6 to 12, and 12 to 24 hours postdose on Days 1, 7, and 14

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 (实际的)

2018年3月21日

初级完成 (实际的)

2018年10月9日

研究完成 (实际的)

2018年10月10日

研究注册日期

首次提交

2018年3月7日

首先提交符合 QC 标准的

2018年3月7日

首次发布 (实际的)

2018年3月13日

研究记录更新

最后更新发布 (实际的)

2020年11月18日

上次提交的符合 QC 标准的更新

2020年11月17日

最后验证

2020年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • BOS172767-01
  • 2017-004002-18 (EudraCT编号)
  • QCL118174 (其他标识符:Quotient Study Number)

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

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