Study of TV-1106 in Growth Hormone-Deficient Adults
Status: | Terminated |
---|---|
Conditions: | Endocrine |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 7/11/2018 |
Start Date: | April 2015 |
End Date: | December 2015 |
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Efficacy, Safety, and Tolerability Study of TV-1106 in Growth Hormone-Deficient Adults Who Are Not Current Users of rhGH Treatment
The primary objective of this study is to determine the efficacy of 6 months of treatment
with TV-1106 compared with placebo on body fat composition.
with TV-1106 compared with placebo on body fat composition.
Inclusion:
- males and females 18 years of age or over
- diagnosis of adult growth hormone deficiency (GHD) for at least 6 months, or patients
who have hypopituitarism from surgical resection
- no history of exposure to any rhGH within the past 12 months prior to screening
- stable, adequate doses of replacement hormones (adrenal, thyroid, estrogen,
testosterone, vasopressin) for at least 3 months prior to screening
- Other criteria apply, please contact the investigator for more information
Exclusion:
- patients with acute or chronic conditions or diseases that could confound results of
the study or put the patient at undue risk as determined by the investigator
- Presence of contraindications to rhGH treatment
- patients who have participated in another clinical trial with a new
chemical/biological entity within 3 months of screening
- patients with known active malignancy (excluding surgically removed basal cell
carcinoma or carcinoma in situ of cervix)
- patients with a previously treated pituitary tumor with evidence of tumor progression
in the past year patients with a new diagnosis of pituitary adenoma or other
intracranial tumor within 12 months of screening
- presence of Prader-Willi syndrome, Turner's syndrome, untreated adrenal insufficiency,
active acromegaly in the past 5 years, or active Cushing's syndrome in the past 1 year
- patients with type 1 diabetes mellitus or poorly controlled type 2 diabetes mellitus
as indicated by a glycated hemoglobin (HBA1c) of ≥8%
- patients using weight reducing agents or appetite suppressants
- women who are pregnant or nursing, or planning pregnancy during the study period
- Other criteria apply, please contact the investigator for more information
We found this trial at
27
sites
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