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Completed

NCT Number: NCT02146625

Safety, Tolerability, PK, PD, ADA of Escalating Single Dose of CJ-40002 in Healthy Male Subjects

The objectives of this study are:

* To evaluate the safety and tolerability of CJ-40002 after single SC injection in healthy male volunteers. * To evaluate the PK of CJ-40002 after single SC injection in healthy male volunteers. * To evaluate the PD of CJ-40002 after single SC injection in healthy male volunteers. * To evaluate the ADA of CJ-40002 after single SC injection in healthy male volunteers.

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Key information

Conditions

Age range

19 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy male volunteers in the age between 19 and 45 years old (inclusive)
  • Body mass index (BMI) in the range of 18.5 to 25 kg/m2 and weighing at least 55 kg
  • Subject who have voluntarily agreed to participate in the trial and signed the written informed consent form, after having listened to the purpose, method, and effect of the clinical trial

Exclusion criteria

  • History of clinically significant gastrointestinal, renal, hepatic, neurologic, hematologic, endocrine, oncologic, pulmonary, immunologic, psychiatric, musculoskeletal or cardiovascular disease or any other condition
  • History of allergy or sensitivity to any drug
  • Subject with the following clinically significant laboratory abnormalities:
  • AST or ALT > 1.25 x Upper Limit Normal (ULN)
  • Total bilirubin > 1.5 x Upper Limit Normal (ULN)
  • CPK > 1.5 x Upper Limit Normal (ULN)
  • eGFR < 60 mL/min/1.73 m2
  • Systolic blood pressure outside the range of 90 to 150 mmHg or diastolic blood pressure outside the range of 50 to 100 mmHg
  • History of drug abuse
  • History of caffeine, alcohol, smoking abuse
  • Participation in any clinical investigation within 60days prior to study medication dosing
  • Subjects with whole blood donation within 60days, component blood donation within 30days prior to study medication dosing
  • Positive test results for HBs Ab, HCV Ab, HIV test
  • Subjects considered as unsuitable based on medical judgement by investigators

Treatment and study plan

CJ-40002

Drug

Primary outcomes

  1. Pharmacokinetics: AUC, Cmax

    Time frame: 15 days

  2. Safety and Tolerability (AE's, vital signs, ECG, laboratory tests, local reaction)

    Time frame: 29 days

Secondary outcomes

  1. Pharmacokinetics: Tmax, T1/2, CL/F, Vd

    Time frame: 15 days

  2. Pharmacodynamics: Serum IGF-1, free IGF-1, IGFBP-3, GHBP

    Time frame: 15 days

  3. Formation of anti-drug antibodies

    Time frame: 29 days

Sponsors and collaborators

Lead sponsor

HK inno.N Corporation

Industry

Registry information

Official study title

A Dose-block Randomized, Single-blind, Placebo-controlled, Single-dosing, Dose-escalation Phase I Clinical Trial to Investigate the Safety/Tolerability and Pharmacokinetics/Pharmacodynamics of CJ-40002 After Subcutaneous Injection in Healthy Adult Male Volunteers

Acronym: hGH

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
May 26, 2014
Registry last updated
Dec 29, 2016

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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