Treatment of Adults With Growth Hormone Deficiency
Launched by LG LIFE SCIENCES · Jan 15, 2008
Trial Information
Current as of April 30, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients (male and female) who have completed the Visit 8 of preceding main study (BPLG-005) and are willing to continue their participation in an extension study
- • If female, women of child-bearing potential who are using a reliable method of contraception and be willing to use it throughout the study. A negative urine pregnancy test at Visit 0 is required for females of child-bearing potential
- • Written informed consent of the patient
- Exclusion Criteria:
- • Evidence of active malignancy or growth of a previously stable tumor
- • Benign intracranial hypertension
- • Clinically significant respiratory, cardiac, hepatic, renal, neuromuscular disease
- • Non-compliance with medications, un-cooperativeness or drug abuse during the BPLG-005 study
- • Patients who are not able to comply with the study protocol for any reason
About Lg Life Sciences
LG Life Sciences is a leading global biopharmaceutical company dedicated to the research, development, and commercialization of innovative therapies across a range of therapeutic areas, including oncology, immunology, and infectious diseases. As a subsidiary of LG Corporation, LG Life Sciences leverages cutting-edge technology and a strong commitment to quality to advance its clinical trials and deliver effective solutions to unmet medical needs. With a focus on scientific excellence and patient-centric approaches, the company strives to enhance global health outcomes through strategic partnerships and robust clinical research initiatives.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
HJ Ji, PhD
Study Chair
LG Life Sciences
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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