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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01213381
Other study ID # TED11451
Secondary ID U1111-1117-3152
Status Completed
Phase Phase 1
First received September 30, 2010
Last updated May 23, 2013
Start date September 2010
Est. completion date February 2013

Study information

Verified date May 2013
Source Sanofi
Contact n/a
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

Primary Objective:

- To determine a dose of SAR240550 to be further studied in combination with chemotherapy regimens

Secondary Objectives:

- To determine the dose limiting toxicity (DLT) of SAR240550 and SAR240550 in combination with chemotherapy regimen (gemcitabine and carboplatin

- To assess safety profiles: significant laboratory changes and adverse events (AEs)

- To make a preliminary assessment of antitumor effect in study subjects per Response Evaluation Criteria in Solid Tumors (RECIST) with measurable disease

- To characterize SAR240550 and metabolites, 4-iodo-3-amino benzamide (IABM) and 4-iodo-3-amino-benzoic acid (IABA), pharmacokinetics

- To collect blood samples for glutathione S-transferase (GST) genotypes at baseline)

Based on data generated by BiPar/Sanofi, it is concluded that iniparib does not possess characteristics typical of the PARP inhibitor class. The exact mechanism has not yet been fully elucidated, however based on experiments on tumor cells performed in the laboratory, iniparib is a novel investigational anti-cancer agent that induces gamma-H2AX (a marker of DNA damage) in tumor cell lines, induces cell cycle arrest in the G2/M phase in tumor cell lines, and potentiates the cell cycle effects of DNA damaging modalities in tumor cell lines. Investigations into potential targets of iniparib and its metabolites are ongoing.


Description:

The duration of the study for each patient will include an up to 4-week screening phase, 21-day study cycle(s), followed by a 30 day follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date February 2013
Est. primary completion date February 2013
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion criteria:

- Histologically or cytologically documented advanced solid tumor that was refractory to standard therapy or for which no standard therapy is available

Exclusion criteria:

- Eastern Cooperative Oncology Group (ECOG) performance status of =2

- Known hematological malignancies

- Symptomatic or untreated brain metastases requiring concurrent treatment, inclusive of but not limited to surgery, radiation, and corticosteroids

- Myocardial infarction within 6 months of study Day 1, unstable angina, congestive heart failure with New York Heart Association >class II, uncontrolled hypertension

- Active human immunodeficiency virus infection, hepatitis C virus, or chronic hepatitis B infection

- Major surgery within 28 days of study Day 1

- Not recovered from all previous therapies (i.e. radiation, surgery, and medications)

- Adverse events related to previous therapies must be Common Terminology Criteria for Adverse Events (CTCAE) grade = 1 (except alopecia) at screening or returned to the subject's baseline prior to their most recent previous therapy

- Inadequate organ and bone marrow function Radiation therapy within 14 days of study Day 1

- Chemotherapy or antibody therapy for treatment of underlying malignancy within 21 days of study Day 1

- Concurrent or prior (within 7 days of study Day 1) anticoagulation therapy

- Currently enrolled or was enrolled within 30 days of completing other investigational drug study, or receiving other investigational agent not approved for any indications

- Subject who had been previously enrolled in this study . Not available for follow-up assessment

- Any kind of disorder that compromised the ability of the subject to give written informed consent and/or comply with the study procedures

- Patient who is judged by the investigator as not suitable for participation in the study

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Iniparib (SAR240550 - BSI-201)
Pharmaceutical form:sterile aqueous solution Route of administration: intravenous
Gemcitabine
Pharmaceutical form:sterile aqueous solution Route of administration: intravenous
Carboplatin
Pharmaceutical form:sterile aqueous solution Route of administration: intravenous

Locations

Country Name City State
Japan Sanofi-Aventis Investigational Site Number 392001 Kobe-Shi
Japan Sanofi-Aventis Investigational Site Number 392002 Matsuyama-Shi

Sponsors (1)

Lead Sponsor Collaborator
Sanofi

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dose Limiting Toxicity in cycle 1 3 Weeks Yes
Secondary Efficacy assessment as tumor response defined by Response Evaluation Criteria in Solid Tumors (RECIST) 30 days after the last injection No
Secondary Safety based on clinical and laboratory tests and Adverse Events (AEs) 30 days after the last injection Yes
Secondary Pharmacokinetics of SAR240550 Cycle 1 and Cycle 2 No
Secondary Pharmacodynamics of SAR240550 Cycle1, Cycle 2 and 30 days after the last injection No
Secondary Pharmacogenomic analysis of glutathione S-transferase (GST) genotypes Cycle 1 No