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临床试验/NCT03309605
NCT03309605已完成1 期

A Phase 1, Randomized, Double-Blinded, Placebo-Controlled, Third Party Open, Multiple Dose Escalation, Single Center Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Subcutaneously Administered ELX-02 in Independent Consecutive Cohorts of Healthy Subjects

Eloxx Pharmaceuticals, Inc.1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2017年10月11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
入组人数
62
试验地点
1
主要终点
Pharmacokinetic Parameter - Plasma AUC0-inf

研究概览

简要总结

Phase 1 Multiple Ascending Dose Study in Normal Healthy Volunteers

详细描述

This is a study in humans of ELX-02, an advanced synthetic aminoglycoside optimized as a translational read-through drug (TRID) for the treatment of genetic conditions caused by nonsense mutations. This is a classical Phase 1b study designed as a randomized, double-blinded, placebo-controlled, multiple dose escalation to evaluate the safety, tolerability, and pharmacokinetics of ELX-02 in healthy adult volunteers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 55 Years(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

Placebo Comparator Arm

Placebo Comparator

Placebo

干预措施: Placebo (Drug)

ELX-02

Experimental

ELX-02

干预措施: ELX-02 (Drug)

结局指标

主要结局

Pharmacokinetic Parameter - Plasma AUC0-inf

时间窗: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post dose

Day 29 Area under the curve (AUC0-inf) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 29 extrapolated to infinity

Pharmacokinetic Parameter Plasma - Tmax

时间窗: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post-dose

Day 29 Time to maximum concentration (Tmax) of ELX-02 plasma concentrations following the subcutaneous (SC) dose on Day 29

Urine Pharmacokinetics Parameter - CLR24h

时间窗: 24 h

Renal clearance on Day 29 (CLR=Ae24h/plasmaAUC24h)

Urine Pharmacokinetics Parameter - Fe 12h on Day 29

时间窗: 12 h on Day 29

Percent of dose excreted (Fe) in urine on Day 29

Pharmacokinetic Parameter - Plasma Tmax

时间窗: Day 1: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post-dose

Day 1 Time to maximum concentration (Tmax) of ELX-02 plasma concentrations following the subcutaneous (SC) dose on Day 1

Pharmacokinetic Parameters - Plasma Cmax

时间窗: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post-dose

Day 29 Peak Plasma Concentration (Cmax) of ELX-02 following the subcutaneous (SC) dose on Day 29 to 72 hours post-dose

Pharmacokinetic Parameter - Plasma Rac(AUC24h)

时间窗: Day 1 and Day 24 hr

Accumulation ratio, calculated as AUC24h Day29/AUC24h Day 1

Pharmacokinetic Parameter - Plasma RAC(Cmax)

时间窗: Day 1 and Day 29

Accumulation ratio, calculated as Cmax Day29/Cmax Day 1

Urine Pharmacokinetics Parameter - Ae72h

时间窗: Day 29: pre-dose and during 0-12h, 12-24h, 24-48h, and 48-72h post-dose

Day 29 Cumulative amount of unchanged drug excreted into urine (Ae72h) of ELX-02 following the subcutaneous (SC) dose on Day 29

Urine Pharmacokinetic Parameter - Rmax

时间窗: Day 29: pre-dose and during 0-12h, 12-24h, 24-48h, and 48-72h post-dose

Day 29 Maximum rate of urinary extraction (Rmax) of ELX-02 in each collection time interval following the subcutaneous (SC) dose on Day 29

Urine Pharmacokinetics Parameter - CLR24h on Day 1

时间窗: 24 hours

Renal clearance on Day 1 (CLR=Ae24h/plasmaAUC24h)

Pharmacokinetic Parameters - Plasma AUC0-24

时间窗: Day 1: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, post-dose

Day 1 Area under the curve (AUC0-24) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 1 to 24 hours post-ose

Pharmacokinetic Parameters- Plasma AUC0-24

时间窗: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, post-dose

Day 29 Area under the curve (AUC0-24) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 29 to 24 hours post-dose

Urine Pharmacokinetics Parameter - Fe12h Day 1

时间窗: 12 hours

Percent of dose excreted (Fe) in urine on Day 1

次要结局

  • Number of Patients Experiencing at Least One Treatment-Emergent Adverse Events (TEAEs)(Day 1-29)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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