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Completed Phase 2 Interventional

Safety, Tolerability and Efficacy of ISIS-GCGRRx in Type 2 Diabetes

ClinicalTrials.gov ID: NCT01885260

Public ClinicalTrials.gov record NCT01885260. 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 3, 2026, 11:28 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 Double Blind, Placebo-Controlled, Phase 2 Study to Assess the Safety, Tolerability and Efficacy of ISIS 449884 Administered Once Weekly to Patients With Type 2 Diabetes Mellitus Being Treated With Metformin

Brief summary

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

The purpose of this study is to evaluate the efficacy, safety and tolerability of ISIS-GCGRRx in combination with metformin versus placebo + metformin

Study identification

NCT ID
NCT01885260
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ionis Pharmaceuticals, Inc.
Industry
Enrollment
77 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Jul 2013 (Type not available)
Primary completion
May 2014 (Actual)
Completion
Nov 2014 (Actual)
Last update posted
Jul 4, 2016

2013 – 2014

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Isis Investigational Site Birmingham Alabama 35216 —
Isis Investigational Site Muscle Shoals Alabama 35662 —
Isis Investigational Site Anaheim California 92801 —
Isis Investigational Site Chino California 91710 —
Isis Investigational Site Los Angeles California 90057 —
Isis Investigational Site DeLand Florida 32720 —
Isis Investigational Site Fort Lauderdale Florida 33306 —
Isis Investigational Site Miami Florida 33143 —
Isis Investigational Site Marietta Georgia 30066 —
Isis Investigational Site Las Vegas Nevada 89101 —
Isis Investigational Site Cincinnati Ohio 45245 —
Isis Investigational Site Oklahoma City Oklahoma 73103 —
Isis Investigational Site Eugene Oregon 97404 —
Isis Investigational Site Corpus Christi Texas 78404 —
Isis Investigational Site Katy Texas 77450 —
Isis Investigational Site Salt Lake City Utah 84107 —
Isis Investigational Site Renton Washington 98057 —
Isis Investigational Site Spokane Washington 99202 —

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01885260, 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 Jul 4, 2016 · Synced Oct 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01885260 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →