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Completed Phase 2 Interventional

Phase 2 Study to Evaluate Safety & Efficacy of VPI-2690B in Diabetic Nephropathy Patients

ClinicalTrials.gov ID: NCT02251067

Public ClinicalTrials.gov record NCT02251067. 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 27, 2026, 3:14 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 Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Parallel Group, Phase 2, Two-Part Adaptive Study to Evaluate the Safety and Efficacy of VPI-2690B Injection in Patients With Nephropathy Due to Diabetes

Brief summary

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

The purpose of this study is to determine whether VPI-2690B Injection is effective in the treatment of diabetic nephropathy.

Study identification

NCT ID
NCT02251067
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vascular Pharmaceuticals, Inc.
Industry
Enrollment
165 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 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
Sep 2014 (Type not available)
Primary completion
Mar 2017 (Actual)
Completion
Mar 2017 (Actual)
Last update posted
Mar 28, 2017

2014 – 2017

United States locations

U.S. sites
32
U.S. states
18
U.S. cities
32
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Little Rock Arkansas — —
Not listed La Mesa California — —
Not listed Riverside California — —
Not listed Sacramento California — —
Not listed Tustin California — —
Not listed Cooper City Florida — —
Not listed Coral Springs Florida — —
Not listed Hialeah Florida — —
Not listed Miami Florida — —
Not listed St. Petersburg Florida — —
Not listed Winter Park Florida — —
Not listed Columbus Georgia — —
Not listed Idaho Falls Idaho — —
Not listed Mount Prospect Illinois — —
Not listed Peoria Illinois — —
Not listed Merrillville Indiana — —
Not listed Boston Massachusetts — —
Not listed Flint Michigan — —
Not listed Kansas City Missouri — —
Not listed Las Vegas Nevada — —
Not listed Albany New York — —
Not listed Asheville North Carolina — —
Not listed Greenville North Carolina — —
Not listed Morehead City North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Wooster Ohio — —
Not listed Allentown Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed El Paso Texas — —
Not listed San Antonio Texas — —

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02251067, 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 Mar 28, 2017 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02251067 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →