Treatment Extension Study for Patients Who Have Previously Participated and Have Benefited From Iniparib in a Clinical Trial
Diagnosis: Breast: Early Stage Disease
NCT ID: NCT01593228
(View complete trial on ClinicalTrials.gov)
DFCI Protocol ID: 12-383
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.
Faulkner Hospital, Dana-Farber Cancer Institute
Daniel Morganstern, MD,
Dana-Farber Cancer Institute:
Breast Cancer Nursing Team, 617-632-3478
Inclusion criteria :
- 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
- 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
- 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
- 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.