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Completed Phase 2 Interventional

Safety and Efficacy of Biphasic Remogliflozin Etabonate in the Treatment of Type 2 Diabetes

ClinicalTrials.gov ID: NCT02537470

Public ClinicalTrials.gov record NCT02537470. 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 9, 2026, 2:55 PM 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 12-week Randomized, Double-blind, Parallel-group, Placebo-controlled Study to Determine the Efficacy and Safety of Biphasic Remogliflozin Etabonate When Administered to Subjects With Type 2 Diabetes Mellitus

Brief summary

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

This is a dose-ranging study to evaluate the efficacy, safety and tolerability of a range of doses of a biphasic formulation of remogliflozin etabonate compared to placebo, administered over 12 weeks in subjects with type 2 diabetes mellitus.

Study identification

NCT ID
NCT02537470
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
BHV Pharma
Industry
Enrollment
191 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 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 2015 (Type not available)
Primary completion
Aug 2016 (Actual)
Completion
Aug 2016 (Actual)
Last update posted
Jan 18, 2018

2015 – 2016

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Advanced Arizona Clinical Research Tucson Arizona 85712 —
Long Beach Clinical Trials Long Beach California 90806 —
Long Beach Center for Clinical Research Long Beach California 90807 —
National Research Institute Los Angeles California 90057 —
Orange County Research Center Tustin California 92780 —
Diablo Clinical Research Walnut Creek California 94598 —
Chase Medical Research Waterbury Connecticut 06708 —
Medical Research Unlimited Hialeah Florida 33012 —
Progressive Medical Research Port Orange Florida 32127 —
Meridien Research Tampa Florida 33634 —
eStudySite, Las Vegas Las Vegas Nevada 89109 —
Comprehensive Clinical Research Berlin New Jersey 08009 —
Albuquerque Clinical Trials, Inc Albuquerque New Mexico 87102 —
Mountain View Clinical Research Greer South Carolina 29651 —
New Phase Research & Development Knoxville Tennessee 37909 —
Austin Center for Clinical Research Austin Texas 78756 —
Padre Coast Clinical Research Corpus Christi Texas 78404 —
Juno Research, LLC Houston Texas 77074 —
Wasatch Clinical Research Salt Lake City Utah 84107 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02537470, 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 Jan 18, 2018 · Synced Oct 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02537470 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →