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Completed Phase 3 Interventional

Treatment Extension Study for Patients Who Have Previously Participated and Have Benefited From Iniparib in a Clinical Trial

ClinicalTrials.gov ID: NCT01593228

Public ClinicalTrials.gov record NCT01593228. 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 21, 2026, 6:23 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

International, Multi-Center, Open-label, Treatment Extension Study of Iniparib as Monotherapy or in Combination Chemotherapeutic Regimens in Cancer Patients Who Have Derived Clinical Benefit From Iniparib Following Completion of a Phase 1, 2 or 3 Parental Study

Brief summary

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

The purpose of this study is to assess the safety and tolerability of iniparib administered as monotherapy or in combination regimens in patients previously treated with iniparib in a clinical study and who have derived clinical benefit after completion of the parental study's objectives.

Study identification

NCT ID
NCT01593228
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
37 participants

Conditions and interventions

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
May 2012 (Type not available)
Primary completion
Sep 2016 (Actual)
Completion
Sep 2016 (Actual)
Last update posted
Sep 19, 2017

2012 – 2016

United States locations

U.S. sites
29
U.S. states
23
U.S. cities
28
Facility City State ZIP Site status
Investigational Site Number 840013 Birmingham Alabama 35205 —
Investigational Site Number 840033 Santa Maria California 93454-8903 —
Investigational Site Number 840046 Vallejo California 94589 —
Investigational Site Number 840008 Denver Colorado 80218 —
Investigational Site Number 840027 Jacksonville Florida 32256 —
Investigational Site Number 840063 Augusta Georgia 30912 —
Investigational Site Number 840055 Tucker Georgia 30084 —
Investigational Site Number 840039 Maywood Illinois 60153 —
Investigational Site Number 840012 Indianapolis Indiana 46227 —
Investigational Site Number 840025 Sioux City Iowa 51105 —
Investigational Site Number 840030 Boston Massachusetts 02115 —
Investigational Site Number 840001 Detroit Michigan 48201 —
Investigational Site Number 840006 Minneapolis Minnesota 55407-3799 —
Investigational Site Number 840002 Jackson Mississippi 39202 —
Investigational Site Number 840059 St Louis Missouri 63110 —
Investigational Site Number 840004 St Louis Missouri 63141 —
Investigational Site Number 840022 Las Vegas Nevada 89169 —
Investigational Site Number 840017 Voorhees Township New Jersey 08043 —
Investigational Site Number 840010 Albany New York 12206 —
Investigational Site Number 840015 Charlotte North Carolina — —
Investigational Site Number 840060 Cincinnati Ohio — —
Investigational Site Number 840043 Cleveland Ohio 44106 —
Investigational Site Number 840021 Pittsburgh Pennsylvania 15213 —
Investigational Site Number 840028 Memphis Tennessee 38120-2146 —
Investigational Site Number 840007 Austin Texas 78731 —
Investigational Site Number 840003 El Paso Texas 79915 —
Investigational Site Number 840019 Plano Texas 75075 —
Investigational Site Number 840005 Norfolk Virginia 23502 —
Investigational Site Number 840009 Vancouver Washington 98684 —

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01593228, 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 Sep 19, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01593228 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →