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Completed

NCT Number: NCT03577509

Single Dose Escalations Study of Amphotericin B Colloidal Dispersion In Healthy Subjects in China

The purpose of this trial is to evaluate the pharmacokinetics of single intravenous of Amphotericin B Colloidal Dispersion(ABCD)in Chinese healthy subjects.

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Key information

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Huashan Hospital Affiliated to Fudan University

Shanghai, Shanghai Municipality, 200040, China

About this study

Primary Objective: Evaluation the pharmacokinetics, safety and tolerability of single intravenous of ABCD in Chinese healthy subjects.

Secondary Objective: Evaluation the safety and tolerability of single intravenous of ABCD in Chinese healthy subjects.

Exploratory Objective:Evaluation the effect of single intravenous ABCD on early renal injury indicators (KIM-1 and cystatin C) in Chinese healthy subjects.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Body mass index (BMI) of 19 to 26 kg/m2, inclusive 19 and 26. BMI = weight (kg)/[height(m)]2.
  • Subjects are fully informed and voluntarily consent to participate in this study.

Exclusion criteria

  • History of allergy or hypersensitivity.
  • Presence of any acute or chronic medical condition within 3 months prior to investigational products administration, including but not limited to: hepatic, gastrointestinal, renal, hematologic (including coagulation), pulmonary, neurologic, respiratory, endocrine, or cardiovascular system abnormalities; psychiatrical disease including major psychiatric disorders (e.g., schizophrenia, bipolar disorder); acute infection; or other conditions that would interfere with the absorption, distribution, metabolism, or excretion of drugs.
  • During the screening period, abnormal and clinically significant of physical examination, vital signs, laboratory examination, etc.
  • A positive result in hepatitis B surface antigen (HBsAg), hepatitis B e antigen (HBeAg), anti-hepatitis C virus (HCV) antibodies, a syphilis test, or an human immunodeficiency virus (HIV) test.
  • Lost blood or donated more than 400 mL of blood within 3 months prior to the screening.
  • Participation in a clinical drug study 30 days prior to present study.
  • Use of any other drugs within 2 weeks prior to the screening.
  • Subjects planning to give birth or donate sperm during the study or within 3 months after the study.
  • The partner of the subject is unwilling to take effective contraceptive measures.
  • Other unfavorable factors diagnosed by investigators.

Treatment and study plan

ABCD

Drug

Intravenous infusion of dexamethasone 5mg before ABCD intravenous administration; Single infusion.

Primary outcomes

  1. Pharmacokinetics of single infusion of ABCD

    Time frame: before infusion and at the midpoint and end of the infusion;and at 15 and 30 min;1,2,4,7,10,24,48,72,120,168,240,336,408,504,576 and 672hour postinfusion

    Peak Plasma Concentration,.

  2. Pharmacokinetics of single infusion of ABCD

    Time frame: before infusion and at the midpoint and end of the infusion;and at 15 and 30 min;1,2,4,7,10,24,48,72,120,168,240,336,408,504,576 and 672hour postinfusion

    Area under the plasma concentration versus time curve

Sponsors and collaborators

Lead sponsor

CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

Industry

Registry information

Official study title

Pharmacokinetics, Safety and Tolerability of Single Infusion of Amphotericin B Colloidal Dispersion In Healthy Subjects in China

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Jul 5, 2018
Registry last updated
Oct 9, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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