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Completed

NCT Number: NCT01093742

A Study of HM10560A in Healthy Male Subject

* Study Design

* Randomized, Double-blind, Placebo-controlled, escalating single-dose design. * Four ascending dose cohorts. * In each cohort, subjects will be randomized to receive a single dose of HM10560A or placebo (negative control). * Objectives

* The primary objective of the study is to assess the safety and tolerability of single escalating subcutaneous doses of HM10560A in healthy male subjects.

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Key information

Conditions

Age range

20 year–54 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Medical Center

Seoul, South Korea

About this study

The secondary objectives of the study are as follows:

  • To assess the pharmacokinetics(PK) and pharmacodynamics(PD) of a single subcutaneous dose of HM10560A.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy male volunteers, age range 20 to 54 years are informed of the investigational nature of this study and voluntarily agrees to participate in this study
  • Body mass index of ≥19 and ≤26 Subject
  • Medically healthy with no clinically significant screening results through Physical examination, 12 lead ECG, Laboratory test
  • Able to participate in all procedure
  • SBP 90-140 mmHg, DBP 60-90 mmHg, Pulse rate 50-90 times/min
  • AST, ALT <1.5 X UNL, CPK < 2 X UNL
  • Able to abstain from alcohol and smoke during study period
  • Consented to contraception until 2 month after end of the study

Exclusion criteria

  • Acute infection history within 14 days
  • Prior exposure or hypersensitivity to recombinant human growth hormone
  • Positive findings on HBsAg, Anti-HAV IgM, anti-HCV, HIV Ag, HIV Ab and syphilis high quality regain test
  • History of significant gastrointestinal, cardiac, pulmonary, hepato- and nephro- disease
  • psychiatric disorder, malignancy tumor, hormonal disorder, diabetes mellitus and hypertension or history of immunosuppressant treatment
  • Caffeine, alcohol and smoke abuse
  • History of hemophilia or anticoagulant treatment
  • Revulsion and/or panic about syringe needle and hypersensitivity to subcutaneously administration
  • History drug abuse or positive testing for amphetamine, barbiturate, cocaine, opiates, benzodiazepines
  • Blood donation or significant blood loss within 60 days prior to Day 1. Plasma donation or transfusion within 30 days prior to Day 1.
  • Receipt of another investigational medication within 60 days prior to Day 1
  • Use of any herbal products within 30 days or prescription medication within 14 days or over-the-counter medication within 7 days prior to the Day 1.
  • Subjects who are unlikely to comply with the protocol requirements, instructions and study related restrictions

Treatment and study plan

HM10560A

Drug

Subcutaneously administrate at 0 hour on Day 1

Placebo

Drug

Placebo

Primary outcomes

  1. Safety

    Time frame: 1, 2, 3, 5, 7, 11, 15, 22, 29 day after administration

    Investigate Safety of HM10560A:

    • Physical examination, Laboratory test, ECG, Vital sign, Adverse event, Local tolerability

Sponsors and collaborators

Lead sponsor

Hanmi Pharmaceutical Company Limited

Industry

Registry information

Official study title

A Dose Block-randomized, Double-blind, Placebo-controlled, Single Dosing, Dose-escalation Phase I Clinical Trial to Investigate the Safety, Tolerability and Pharmacokinetics of HM10560A After S.C. Administration in Healthy Male Subjects

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Mar 26, 2010
Registry last updated
Feb 7, 2014

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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