Clinical TrialID 4789

Safety of Subcutaneous Testosterone Enanthate in Adult Male Hypogonadism

NCT02777242

Hypogonadism

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
4789
Evidence Id
4789
Core Evidence Id
4789
Source Clinical Trial Id
4762
Herb2 Clinical Trial Id
HBCT004762
Nct Id
NCT02777242
Title
Safety of Subcutaneous Testosterone Enanthate in Adult Male Hypogonadism
Status
Completed
Phase
Phase 2
Study Result
Yes
Study Condition
Hypogonadism
Study Type
Interventional
Study Design
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Intervention
COMBINATION_PRODUCT: Testosterone enanthate auto-injector
Intervention Allocation
Intervention Model
Single_Group
Intervention Mask
Intervention Purpose
Treatment
Gender
Male
Age
Adult, Older_Adult
Enrollment
66
Outcome Measure
Number of Patients With Adverse Events Receiving Testosterone Enanthate Via QST Auto-injector., Intended users were patients experiencing an adverse event that was considered to be a TEAE if the adverse event started on or after randomization, or existed prior to randomization and worsened in severity or relatedness to QST (QuickShot® Testosterone auto-injector) after randomization., 3 weeks
Sponsor Collaborator
Antares Pharma Inc.
Funded By
INDUSTRY
Location
Birmingham, Alabama, 35235, United States|New York, New York, 10016, United States|Columbus, Ohio, 43213, United States
Other Id
QST-16-006
Start Date
2016-06
Primary Completion Date
2016-08
Completion Date
2016-08
First Posted
2016-05-19
Results First Posted
2018-02-26
Last Update Posted
2018-03-22
Study Document
Study Url
https://clinicaltrials.gov/study/NCT02777242
Title Cn
Title En
Safety of Subcutaneous Testosterone Enanthate in Adult Male Hypogonadism
Bilingual Status
semi_complete