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临床试验/NCT06378125
NCT06378125已完成1 期

A Phase I, Double-blind, Randomised, Placebo-controlled, Single-ascending and Multiple-ascending Dose Trial to Evaluate the Safety and Pharmacokinetics of Oral Controlled-ileal-release Nicotinic Acid (CIR-NA) Compared to Immediate-release Nicotinic Acid and Placebo in Healthy Subjects and Subjects With Prediabetes

University Hospital Schleswig-Holstein1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年12月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
Blood GGT

研究概览

简要总结

A double-blind, randomised, placebo-controlled, single-ascending and multiple-ascending dose trial to evaluate the safety and pharmacokinetics of oral controlled-ileal-release nicotinic acid (CIR-NA) compared to immediate-release nicotinic acid and placebo in healthy subjects and subjects with prediabetes.

详细描述

Recently, administration of one form of vitamin B3, Nicotinamide (NAM), has been shown to improve the host-microbiome interaction in a mouse model, especially when administered in a controlled-release formulation targeting the ileocolic region. Thus, NAM and also the other form of vitamin B3, Nicotinicacid (NA), were identified as promising candidates for a gut-targeted microbiome intervention.

As the upper gastrointestinal tract efficiently absorbs amino acids and vitamins, simply increasing the NA and/or NAM content in human food would not be expected to deliver these molecules in sufficient amounts into the lower ileum and colon, where most of the microbiota are located. Moreover, adverse effects such as flushing or gastrointestinal symptoms can occur under high and immediately systemically available dosage of NA. Therefore, the novel CIR-NA formulation will be applied to deliver NA to the lower ileum and colon to tar-get the gut microbiome, while largely avoiding systemic exposure, as the terminal ileum and colon have a much lower absorptive capacity than the stomach and upper small intestine.

Both in the single- and multiple-ascending (SAD/MAD) part of the study, CIR-NA or placebo tablets will be self-administered orally, with daily doses of 100 mg (1 tablet), 200 mg (2 tablets), 500 mg (5 tablets) or 1,000 mg CIR-NA (10 tablets) or the corresponding amounts of placebo tablets. In the SAD part, an additional dose of 2,000 mg CIR-NA or placebo (20 tablets) will be self-administered.After completion of the SAD and the 200 mg MAD part in healthy subjects, an additional mul-tiple dose part (200 mg/d CIR-NA) in subjects with PreD (MD-PreD part) will start in parallel to the further dose groups of the MAD part.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Other
盲法
Double (Participant, Investigator)

盲法说明

Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

healthy subjects healthy subjects

Experimental

single-ascending and multipleascending doses (SAD/MAD)

干预措施: immediate-release nicotinic acid (SAD) (Drug)

healthy subjects healthy subjects

Experimental

single-ascending and multipleascending doses (SAD/MAD)

干预措施: controlled-ileal-release nicotinic acid (SAD/ MAD/MD) single- and multiple-ascending dose (SAD/MAD) or multiple dose (MD) (Drug)

healthy subjects healthy subjects

Experimental

single-ascending and multipleascending doses (SAD/MAD)

干预措施: Placebo controlled-ileal-release nicotinic acid (SAD/MAD) (Drug)

healthy subjects healthy subjects

Experimental

single-ascending and multipleascending doses (SAD/MAD)

干预措施: Placebo immediate-release nicotinic acid (SAD) (Drug)

subjects with prediabetes

Experimental

multiple dose (MD)

干预措施: controlled-ileal-release nicotinic acid (SAD/ MAD/MD) single- and multiple-ascending dose (SAD/MAD) or multiple dose (MD) (Drug)

结局指标

主要结局

Blood GGT

时间窗: up to 60 days

Gamma glutamyl transferase (GGT) in U/l

Treatment-Emergent Adverse Events [Safety and Tolerability]

时间窗: up to 60 days

Adverse Events (AEs) during treatment period

Treatment-Emergent Serious Adverse Events [Safety and Tolerability]

时间窗: up to 60 days

Serious Adverse Events (SAEs) during treatment period

Haemoglobin

时间窗: up to 60 days

Haemoglobin (Hb) in %

White blood cells

时间窗: up to 60 days

White blood cell (WBC) count as x10\^9/l

Blood creatinine

时间窗: up to 60 days

Blood Creatinine in mmol/L

Blood urea

时间窗: up to 60 days

Urea in mmol/L

Blood uric acid

时间窗: up to 60 days

Uric acid in mmol/L

Glomerular filtration rate

时间窗: up to 60 days

Glomerular filtration rate (GFR, automatically calculated by the laboratory based on creatinine values) GFR in ml/min/1.73m2

Blood ALT

时间窗: up to 60 days

Alanine transaminase (ALT) in U/l

Blood AST

时间窗: up to 60 days

Aspartate transaminase (AST) in U/l

次要结局

未报告次要终点

研究者

发起方
University Hospital Schleswig-Holstein
申办方类型
Other
责任方
Sponsor

研究点 (1)

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