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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Notify MeKey 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
Primary outcomes
-
Pharmacokinetics: AUC, Cmax
Time frame: 15 days
-
Safety and Tolerability (AE's, vital signs, ECG, laboratory tests, local reaction)
Time frame: 29 days
Secondary outcomes
-
Pharmacokinetics: Tmax, T1/2, CL/F, Vd
Time frame: 15 days
-
Pharmacodynamics: Serum IGF-1, free IGF-1, IGFBP-3, GHBP
Time frame: 15 days
-
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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