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临床试验/NCT06939608
NCT06939608招募中不适用

Kinetics of Yohimbine in Humans to Explore Sex and CYP2D6 Genotype Interactions - YOKI-1 Study

University Medicine Greifswald2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年4月28日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
2
主要终点
Yohimbine plasma concentration expressed as area under the curve (AUC₀-₂₄h) - arm 1 vs. arm 3

研究概览

简要总结

This study investigates the pharmacokinetics of yohimbine in women and men aged 18 to 40 years to explore sex-specific differences in CYP2D6-dependent drug metabolism. Participants will be classified by their CYP2D6 genotype into extensive metabolizers (EM) and poor metabolizers (PM), forming four distinct study arms:

Arm 1) Women, Poor Metabolizers (PM) n=13 Arm 2) Women, Extensive Metabolizers (EM) n=5 Arm 3) Men, Poor Metabolizers (PM) n=13 Arm 4) Men, Extensive Metabolizers (EM) n=5

Each study arm will receive a single oral dose of 50 µg yohimbine (2 x 1 tablets, 25 µg per tablet) and 25 mg of ¹³C₃-caffeine co-administered as a drinking solution.

The purpose of this study is:

  1. To characterize the pharmacokinetics of yohimbine following a single oral dose in women and men across different CYP2D6 phenotypes.
  2. To evaluate yohimbine's suitability as a reliable probe for assessing CYP2D6 activity.
  3. To investigate potential interactions between CYP2D6 and CYP1A2, as well as interindividual variability in CYP1A2-dependent caffeine metabolism.

详细描述

The study is designed as an open-label, single-dose protocol with four study arms based on sex and CYP2D6 genotype. A single oral dose of yohimbine and ¹³C₃-caffeine will be administered with 240 ml of still water under overnight fasting conditions.

A total of 19 blood samples will be collected at defined time points (baseline; 10; 20; 30; 40; 50; 60; 70; 80; 90; 100; 110 min; 2; 3; 4; 6; 8; 10; 24 h). At each time point, 4.9 mL of blood will be drawn for plasma separation to determine yohimbine, the primary metabolite 11-OH-yohimbine and 13C₃-caffeine with associated CYP1A2 dependent metabolites. One additional blood sample (EDTA tube) for potential future genetic analysis, will be collected together with the baseline kinetic samples.

For each participant, a total of approximately 98 mL of blood will be collected during the kinetic visits and an additional 12 mL during the screening visit.

Following the administration of yohimbine and 13C3-caffeine, participants will consume 200 mL of sparkling water every hour to stimulate gastrointestinal peristalsis facilitate substance transport. Two hours post-administration, participants may have a cup of tea or coffee, while a standardized meal will be served four hours after dosing.

Urine samples will be collected over 24 hours in three intervals (0-4 h, 5-10 h, 11-24 h). Blood pressure and heart rate monitoring will be conducted during the initial four hours and participants will remain in the Clinical Research Unit of the Institute of Pharmacology for the first 10 hours post-administration. At 24 hours post-dosing, participants will return to the Clinical Research Unit for the final scheduled blood collection and to provide their last urine sample (11-24 h).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

盲法说明

This is an open-label study; no parties involved are masked.

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • individuals of both biological sexes, assigned as women or men at birth
  • age: ≥ 18 and ≤ 40 years
  • possesses the ability to understand the study purpose and design
  • contractually capable and provides signed informed consent form
  • in good general health or with mild and/or well-managed conditions such as allergies, asthma, hypertension or orthopedic diseases
  • taking no more than three chronic medications
  • individuals classified as either extensive metabolizers (EM) or poor metabolizers (PM) based on their CYP2D6 genotype:
  • Extensive Metabolizers (EM):
  • homozygous for CYP2D6 *1,CYP2D6 *2, CYP2D6 *35, or heterozygous combination of any of these alleles
  • Poor Metabolizers (PM):
  • homozygous for CYP2D6 *3, CYP2D6 *4, CYP2D6 *5, CYP2D6 *6, or heterozygous combination of any of these alleles

排除标准

  • BMI > 30 kg/m2 and < 18 kg/m2
  • body weight < 48 kg
  • women: known pregnancy or lactation period; positive urine pregnancy test at screening or kinetic visit
  • men: hemoglobin < 13 g/dl (8,07 mmol/l) women: hemoglobin < 12 g/dl (7,45 mmol/l)
  • elevated liver function tests (1 or more of ALAT, ASAT, yGT, Bilirubin > 2x ULN)
  • reduced renal function (eGFRMDRD < 60 mL/min/1,7 m2)
  • QTcF > 450 ms in screening ECG
  • current or recent psychiatric disorders requiring treatment including depression, bipolar disorder, schizophrenia, psychosis or severe anxiety disorders
  • drug dependency at the time of visit
  • use of recreational drugs more than twice a week
  • any known hypersensitivity or allergic reactions to yohimbine or caffeine
  • history of severe hypersensitivity reactions and/or anaphylaxis
  • poor venous conditions that make it impossible to place a peripheral venous catheter and regularly draw blood through it
  • o) intake of drugs interfering with CYP2D6 and/or CYP1A2 during the past seven days p) intake of yohimbine within 48 hours and caffeine within 16 hours prior to study participation q) engagement in extreme physical activity within 48 hours prior to study participation

结局指标

主要结局

Yohimbine plasma concentration expressed as area under the curve (AUC₀-₂₄h) - arm 1 vs. arm 3

时间窗: 24 hours

Difference in plasma concentrations of yohimbine expressed as area under the curve (AUC₀-₂₄h) between women classified as CYP2D6 poor metabolizers (PM) (arm 1) and men classified as CYP2D6 poor metabolizers (PM) (arm 3).

Yohimbine plasma concentration expressed as area under the curve (AUC₀-₂₄h) - arm 1 vs. arm 2

时间窗: 24 hours

Difference in plasma concentrations of yohimbine expressed as area under the curve (AUC₀-₂₄h) between women classified as CYP2D6 poor metabolizers (PM) (arm 1) and women classified as CYP2D6 extensive metabolizers (EM) (arm 2).

Yohimbine plasma concentration expressed as area under the curve (AUC₀-₂₄h) - arm 3 vs. arm 4

时间窗: 24 hours

Difference in plasma concentrations of yohimbine expressed as area under the curve (AUC₀-₂₄h) between men classified as CYP2D6 poor metabolizers (PM) (arm 3) and men classified as CYP2D6 extensive metabolizers (EM) (arm 4).

次要结局

  • Apparent volume of distribution of yohimbine and 11-OH-yohimbine(24 hours)
  • Cmax of yohimbine and 11-OH-yohimbine(24 hours)
  • tmax of yohimbine and 11-OH-yohimbine(24 hours)
  • Clearance of yohimbine and 11-OH-yohimbine(24 hours)
  • 11-OH-Yohimbine plasma concentration expressed as area under the curve (AUC₀-₂₄h)(24 hours)

研究者

发起方
University Medicine Greifswald
申办方类型
Other
责任方
Principal Investigator
主要研究者

Stefan Engeli, MD

Prof. Dr. med Stefan Engeli

University Medicine Greifswald

研究点 (2)

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