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Safety and Efficacy Study of Recombinant Human Growth Hormone in Adult Growth Hormone Deficiency Patients

Information source: Hanmi Pharmaceutical Company Limited
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Adult Growth Hormone Deficiency

Intervention: HM10560A (Drug); Genotropin (Drug)

Phase: Phase 2

Status: Active, not recruiting

Sponsored by: Hanmi Pharmaceutical Company Limited


The purpose of this study is to assess the safety, tolerability and Pharmacokinetic/ Pharmacodynamic (PK/PD) profile of three doses of HM10560A on an every week (EW) regime and one dose on every other week (EOW) regime administered for a period of 24 weeks initial study.

Clinical Details

Official title: A Phase II, Randomized, Active Controlled, Open Label Study of Safety and Efficacy of HM10560A a Long-acting rhGH-HMC001 Conjugate in Treatment of Subjects Suffering From Adult Growth Hormone Deficiency (AGHD)

Study design: Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Change of IGF-I levels in function of time, and dose strengths

Secondary outcome: IGF-I SDS; changes to baseline in IGF-I SDS

Detailed description:

- To select the optimal dose and dosing regimen of HM10560A for the subsequent phase III

study on the basis of the safety and PK/PD profile after 24 weeks of treatment

- To assess the long term safety of HM10560A when administered in optimal dose range and

dose frequency for additional 48 weeks (followed with 2 weeks safety follow up)


Minimum age: 23 Years. Maximum age: 60 Years. Gender(s): Both.


Inclusion Criteria:

- GHDA subjects, males and females, of age between 23 and 60 years as defined in the

Consensus Guidelines for the Diagnosis and Treatment of Adults with GH Deficiency II (2007) as well as American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for Growth Hormone Use in Growth Hormone-Deficient Adults and Transition Patients (2009);

- r-hGHdrug naïve or any registered or investigational r-hGH replacement therapy was

not given for more than 6 months before the screening.

- Body Mass Index (BMI, kg/m2) of both male and female patients must be between 22. 0 to

35. 0 kg/m2.

- Female patients must have a negative serum pregnancy test at inclusion.

- Confirmed to be negative for anti r-hGH antibodies at the time of screening.

- Willing and able to provide written informed consent prior to performing any study

procedures. Exclusion Criteria:

- Patients with childhood onset of GHD treated with r-hGH before the age of 18.

- Current antitumor therapy.

- Subjects presenting with any clinically significant ECG abnormality.

- Evidence of intracranial hypertension.

- Significant hepatic dysfunction (persistent elevation of alanine transaminase [ALT]

or aspartate transaminase [AST] >1. 5 x upper limit of normal).

- Pregnancy and breastfeeding;

Locations and Contacts

Hanmi, Budapest, Hungary
Additional Information

Starting date: October 2011
Last updated: February 6, 2014

Page last updated: August 23, 2015

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