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Cutoff Assessment for Codeine in Fingerprint Sweat Relative to Oral Fluid, Following Controlled, Oral Administration of Codeine Phosphate Tablets to 40 Healthy Adults

2026年8月5日 更新者:Intelligent Bio Solutions Inc.

This is a prospective, observational, open-label, single-site, in-clinic study with two 20-subject cohorts. Each subject receives two (2) doses of 60mg codeine phosphate in tablet form, the second dose four (4) hours after the first.

The primary objective of this study is to compare data from a fingerprint sweat opiate fluorescence immunoassay screening method to oral fluid opiate screening in subjects dosed with codeine phosphate. Fluorescence measurement data from the fingerprint sweat screening method will be analyzed post hoc to select the fingerprint sweat codeine cutoff best aligned with the oral fluid cutoff.

The secondary objective is to compare LC-MS/MS data from fingerprint sweat specimens and oral fluid in order to select the fingerprint sweat codeine cutoff best aligned with codeine in oral fluid.

研究概览

地位

完全的

条件

详细说明

The Intelligent Fingerprinting Drug Testing System The Intelligent Fingerprinting Drug Testing System utilizes three components for the qualitative determination of codeine in human fingerprint sweat. It is for in vitro diagnostic use only and intended for prescription use indoors by trained personnel. The intended use environment is an indoor office, or an office-like setting such as a portable or prefabricated cabin. The Intelligent Fingerprinting Drug Screening Cartridge, a single-use, lateral-flow immunoassay cartridge, is intended for use with Intelligent Fingerprinting DSR-Plus fluorescence reader. Directly following completion of collecting a full set of 10 fingerprints, the DSC-7 Drug Screening Cartridge is placed in the DSR-Plus fluorescence reader. This test provides only a preliminary result.

Negative results from the Drug Screening cartridge do not require any additional analysis. Non-negative results must be confirmed with a more specific chemical method by using the Sample Collection Cartridge to collect an additional fingerprint sweat specimen. A validated, traceable liquid chromatography/tandem mass spectrometry (LC/MS-MS) method is preferred.

Subjects must be healthy male and non-pregnant female subjects between ages 18 and 55, inclusive, at the time of dosing. Subject body mass index (BMI) must be between 18.0 kg/m2 to 32.0 kg/m2, inclusive, and total weight must be at least 60 kg.

Subjects will check into the clinic the evening prior to codeine phosphate dosing, at least 14 hours prior to dosing, and remain confined in house until at least 24 hours after the initial codeine phosphate dose.

The total number of healthy adult subjects (male and non-pregnant females) required for enrollment in this study protocol is 40. The total duration of the study, from check-in through the end of the study will be approximately 3 days. Subjects will be confined for at least 24 hours after the first codeine dose. Both 60 mg codeine phosphate doses will be given orally in tablet form with 100-120 mL of room temperature water, followed by two oral rinses (rinse and spit) of 30-50 mL water each. 50 mg of naltrexone hydrochloride will be given as a single oral dose with approximately 120 mL of room temperature water at approximately 12 hours (±30 min) prior to the first administration of codeine, again with breakfast at one hour prior to the first codeine phosphate administration, and again 12 hours (±30 min) after the first codeine dose. Additional dose(s) of naltrexone hydrochloride (1 x 50 mg) may be administered at the discretion of the Investigator

Sampling comprises 13 time points for each of fingerprint sweat and oral fluid per subject for opiate content. Baseline biological fluid sampling (fingerprint sweat and oral fluid) will occur within 90 minutes prior to the codeine dosage, then subsequently at 0.5 hours, 1.5, 2.5, 3.5, 4.5, 5.5, 6.5, 7.5, 8.5, 10.5, 12.5 and 24 hours (±15 min) after the codeine phosphate dose. At each time point, specimens will be collected in the order of fingerprint sweat (screening cartridge), oral fluid, and fingerprint sweat on the Sample Collection Cartridge. A handwash and 15-minute wait (following handwash) will precede both fingerprint sweat specimen collections.

Screening results from both fingerprint sweat specimens and oral fluid will be recorded from instrumentation (DSR-Plus) or visual read (OralTox) within 10 minutes of sampling as either a negative or non-negative result. Quantitative codeine concentrations will be determined for the specimens described above using a validated LC-MS/MS method.

研究类型

观察性的

注册 (实际的)

43

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

    • Ontario
      • Mississauga、Ontario、加拿大、L4W 1V7
        • Cliantha Research

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

  • 成人

接受健康志愿者

不

取样方法

非概率样本

研究人群

Subjects will be selected from non-institutionalized persons consisting of members of the community at large.

描述

Inclusion Criteria:

  1. Informed of the nature of the study, agreed to, and able to read, review, and sign the informed consent document prior to dosing. The informed consent document will be written in English; therefore, the subject must have the ability to read and communicate in English.
  2. Completed the screening process within 30 days prior to dosing. Subjects screened as a part of an IRB-approved General Screening Protocol at the clinical research site may be included in this study without additional screening procedures provided all the required screening procedures have been performed within 30 days prior to dosing.
  3. Healthy male and non-pregnant female subjects between ages 18 and 55, inclusive, at the time of dosing.
  4. Body mass index (BMI) between 18.0 kg/m2 to 32.0 kg/m2, inclusive, and weigh at least 60 kg.
  5. Judged by the Investigator and/or designee to be in good health as documented by the medical history, physical examination (including but may not be limited to an evaluation of the cardiovascular, gastrointestinal, respiratory and central nervous systems), vital sign assessments along with oxygen saturation, 12-lead electrocardiogram (ECG), clinical laboratory assessments, and by general observations. Any abnormalities or deviations outside the normal ranges for any of clinical testing (laboratory tests, ECG, etc.) can be repeated at the discretion of the Investigator and/or designee and judged to be not clinically significant for study participation. Any abnormalities or deviations outside the normal range for vital signs can be repeated by clinical staff and judged to be not clinically significant for study participation.
  6. Subjects with glomerular filtration rate (GFR) of greater than or equal to 60.
  7. Females of childbearing potential must be willing to practice an acceptable form of contraception, and have a negative serum pregnancy test at screening and a negative urine pregnancy test on admission to the treatment phase of the study.
  8. Males must agree to practice an acceptable form of contraception.

Exclusion Criteria:

  1. More than three digits absent from the hands due to congenital or accidental cause(s).
  2. Reports receiving any investigational drug/product within 30 days prior to dosing.
  3. Reports any personal history of substance abuse (including drug/alcohol abuse or addiction) or mental illness (e.g. major depression) within one year prior to screening visit.
  4. Reports any presence or history of a clinically significant disorder involving the cardiovascular, respiratory, renal, urologic, gastrointestinal, hepatic, immunologic, hematologic, endocrine, or neurologic system(s) or psychiatric disease as determined by the Investigator.
  5. Presence of any clinically significant results from laboratory tests, vital signs assessments, as judged by the Investigator.
  6. Demonstrates a reactive screen for hepatitis B surface antigen, hepatitis C antibody, or HIV antibody.
  7. Reports a clinically significant illness during the 30 days prior to dosing (as determined by the Investigator).
  8. Reports a history of allergic response(s) to opiates, naltrexone or related drugs.
  9. Reports hypersensitivity to bisulfites.
  10. Reports history of respiratory depression (e.g., sleep apnea).
  11. Current severe hypotension (i.e., systolic blood pressure <90 mmHg).
  12. Reports current presence of acute bronchial asthma/ upper airway obstruction.
  13. If subject reports a history of clinically significant allergies, including food or drug allergies, as judged by the Investigator.
  14. Reports history/current condition of adrenal insufficiency.
  15. Reports history/current condition of renal disease.
  16. Reports a history of smoking within previous six months.
  17. Report history/current condition of seizures, increased intracranial pressure, brain tumor, head injuries or impaired consciousness.
  18. Reports known or suspected gastrointestinal obstruction including, paralytic ileus.
  19. Reports difficulty fasting or consuming standardized meals.
  20. Demonstrates a positive pregnancy screen (females only).
  21. If, in the opinion of the Investigator, the subject is not suitable for the study.

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

队列和干预

团体/队列
干预/治疗
Cohort 1
22 subjects
Measurement of codeine phosphate in oral fluid and fingerprint sweat of dosed subjects
Cohort 2
20 subjects
Measurement of codeine phosphate in oral fluid and fingerprint sweat of dosed subjects

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Fingerprint sweat codeine cutoff
大体时间:Within 24 hours of codeine dosing
Fluorescence measurement data from the fingerprint sweat screening method will be analyzed post hoc to select the fingerprint sweat codeine cutoff best aligned with the oral fluid cutoff.
Within 24 hours of codeine dosing

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。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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)

2026年1月28日

初级完成 (实际的)

2026年2月6日

研究完成 (实际的)

2026年2月6日

研究注册日期

首次提交

2026年8月5日

首先提交符合 QC 标准的

2026年8月5日

首次发布 (实际的)

2026年8月10日

研究记录更新

最后更新发布 (实际的)

2026年8月10日

上次提交的符合 QC 标准的更新

2026年8月5日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • IBS-2025-02

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

是的

在美国制造并从美国出口的产品

不

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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