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

Completed · Phase 3

Conditions studied: Solid Tumors

In brief

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.

Key facts

Study ID: NCT01593228
Run by: Sanofi
People needed: 37
Starts: 2012-05-01
Expected to finish: 2016-09-01
Last updated by the study team: 2017-09-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Cancer patients greater than 18 years of age who have completed all assessments required to meet the primary objectives of a parental phase 1, 2 or 3 clinical study of iniparib as monotherapy or in a combination regimen.
Previously received and are continuing to derive clinical benefit from iniparib, as monotherapy or in combination with chemotherapy, as determined by the treating physician.
Ongoing treatment with iniparib at time of parental study completion/closure and meet criteria to initiate a subsequent cycle of therapy, as described in the parental study protocol.
On a stable parental study regimen (at least one cycle for the regimen at the dose/schedule that is to be given in the Treatment Extension study must have been given prior to the patient's discontinuation from the parental study). Signed written informed consent.

You may not qualify if…

Patient has not previously participated in any clinical trial of iniparib.
Patient has evidence of progressive disease while receiving iniparib.
Patient has another concurrent invasive malignancy (aside from the malignancy for which the patient has received therapy for on the parental protocol).
Patient has a major medical or co-morbid condition(s) that the investigator believes might compromise safe participation in the study (such as uncontrolled lung, kidney, or liver problems; uncontrolled infection; a history of congestive heart failure; or an electrocardiogram suggesting significant problems with the heart).
Patient has not recovered to baseline or less than Grade 1 from non-hematologic adverse events related to any anticancer therapy received prior to signing informed consent on the Treatment Extension study, with the exception of hair loss.
Patient is receiving concurrent treatment with other investigational agents not allowed as part of the combination regimen in the parental study protocol.
Concurrent anticancer treatment with any agent other than iniparib and any co-administered chemotherapeutic agent(s) specified on the parental study protocol are not permitted throughout the course of the study.
Patient is receiving concurrent radiation therapy to treat primary disease with curative intent. (Note that palliative radiotherapy is allowed as long as there is no evidence of progressive disease.)
Patient is unable to comply with the requirements of the study.
Pregnant or breast-feeding women.
Women of childbearing potential or men with partners of childbearing potential who are not protected or who are unwilling to use an effective contraceptive method of birth control during the course of the study and for a period of 6 months following the last dose.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Where it is running

Investigational Site Number 840013 — Birmingham, Alabama, United States
Investigational Site Number 840033 — Santa Maria, California, United States
Investigational Site Number 840046 — Vallejo, California, United States
Investigational Site Number 840008 — Denver, Colorado, United States
Investigational Site Number 840027 — Jacksonville, Florida, United States
Investigational Site Number 840063 — Augusta, Georgia, United States
Investigational Site Number 840055 — Tucker, Georgia, United States
Investigational Site Number 840039 — Maywood, Illinois, United States
Investigational Site Number 840012 — Indianapolis, Indiana, United States
Investigational Site Number 840025 — Sioux City, Iowa, United States
Investigational Site Number 840030 — Boston, Massachusetts, United States
Investigational Site Number 840001 — Detroit, Michigan, United States
Investigational Site Number 840006 — Minneapolis, Minnesota, United States
Investigational Site Number 840002 — Jackson, Mississippi, United States
Investigational Site Number 840059 — St Louis, Missouri, United States
Investigational Site Number 840004 — St Louis, Missouri, United States
Investigational Site Number 840022 — Las Vegas, Nevada, United States
Investigational Site Number 840017 — Voorhees Township, New Jersey, United States
Investigational Site Number 840010 — Albany, New York, United States
Investigational Site Number 840015 — Charlotte, North Carolina, United States
Investigational Site Number 840060 — Cincinnati, Ohio, United States
Investigational Site Number 840043 — Cleveland, Ohio, United States
Investigational Site Number 840021 — Pittsburgh, Pennsylvania, United States
Investigational Site Number 840028 — Memphis, Tennessee, United States
Investigational Site Number 840007 — Austin, Texas, United States

Full record on ClinicalTrials.gov

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