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Terminated Phase 3 Interventional

Study to Assess Safety and Tolerability in Adults With Growth Hormone-Deficiency (GHD)

ClinicalTrials.gov ID: NCT02410356

Public ClinicalTrials.gov record NCT02410356. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 12:09 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Randomized, Open-Label, Comparator-Controlled Study to Assess Safety and Tolerability of Weekly TV-1106 Compared to Daily rhGH (Genotropin(R)) in Adults With Growth Hormone-Deficiency

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study assesses the safety and tolerability of weekly TV-1106 compared to daily rhGH in adults with GHD who have previously been treated with rhGH.

Study identification

NCT ID
NCT02410356
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
34 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2015 (Actual)
Primary completion
Feb 29, 2016 (Actual)
Completion
Apr 30, 2016 (Actual)
Last update posted
Dec 10, 2021

2015 – 2016

United States locations

U.S. sites
32
U.S. states
12
U.S. cities
25
Facility City State ZIP Site status
Teva Investigational Site 13137 Artesia California 90701 —
Teva Investigational Site 13166 Fountain Valley California 33155-6541 —
Teva Investigational Site 13165 Lakewood California 90712 —
Teva Investigational Site 13155 Denver Colorado 80209 —
Teva Investigational Site 13158 Newark Delaware 19713 —
Teva Investigational Site 13162 Fort Lauderdale Florida 33312 —
Teva Investigational Site 13136 Homestead Florida 33030 —
Teva Investigational Site 13138 Miami Florida 33126 —
Teva Investigational Site 13152 Miami Florida 33130 —
Teva Investigational Site 13161 Miami Florida 33145 —
Teva Investigational Site 13500 Miami Florida 33155-6541 —
Teva Investigational Site 13503 Miami Florida 33175 —
Teva Investigational Site 13148 Miami Lakes Florida 33016 —
Teva Investigational Site 13134 Pembroke Pines Florida 33024 —
Teva Investigational Site 13129 West Palm Beach Florida 33401 —
Teva Investigational Site 13135 Detroit Michigan 48202 —
Teva Investigational Site 13146 Henderson Nevada 89052 —
Teva Investigational Site 13147 Las Vegas Nevada 89148 —
Teva Investigational Site 13143 Brooklyn New York 11235 —
Teva Investigational Site 13502 New York New York 10016 —
Teva Investigational Site 13140 New York New York 10032 —
Teva Investigational Site 13128 Asheville North Carolina 28803 —
Teva Investigational Site 13142 Pittsburgh Pennsylvania 15212 —
Teva Investigational Site 13144 Arlington Texas 76014 —
Teva Investigational Site 13163 Dallas Texas 75218 —
Teva Investigational Site 13130 Houston Texas 77079 —
Teva Investigational Site 13141 Houston Texas 77084 —
Teva Investigational Site 13154 Houston Texas 77090 —
Teva Investigational Site 13159 Norfolk Virginia 23507 —
Teva Investigational Site 13504 Federal Way Washington 98003 —
Teva Investigational Site 13164 Seattle Washington 98122 —
Teva Investigational Site 13157 Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02410356, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 10, 2021 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02410356 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →