A Dose Escalation Study of Iniparib as a Single Agent and in Combination in Solid Tumors

NCT ID: NCT01455532

Last Updated: 2014-10-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 59 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-11-30
• Study Completion Date: 2014-04-30

Brief Summary

Primary Objective:

• To assess the safety and the maximum tolerated dose(MTD) of iniparib as a single agent and in combination with chemotherapeutic regimens in patients with advanced solid tumors that are refractory to standard therapy.

Secondary Objectives:

• To assess the antitumor effect of iniparib (per Response Evaluation Criteria in Solid Tumors [RECIST]) Version 1.1 in patients with measurable disease.
• To characterize iniparib (and its metabolites, if possible) pharmacokinetics.

Based on data generated by 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.

Detailed Description

The duration of the study for an individual patient will include a period to assess eligibility (screening period) of up to 4 weeks (28 days), a treatment period of at least 1 cycle (3 weeks or 4 weeks depending on regimen) of study treatment, and an end-of-treatment visit at least 30 days following the last administration of study drug. However, treatment may continue until precluded by toxicity, progression, or death.

Conditions

Neoplasm Malignant

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Iniparib, single agent

Iniparib will be initially administered intravenously once weekly (days 1, 8, and 15) for 3 weeks, in a 21-day cycle. Then, iniparib will be administered twice weekly (days 1, 4, 8, 11, 15, and 18) in a 21-day cycle. Cycle1 (day 1 thru day 21) will be defined as the dose limiting toxicities (DLT) observation period. Starting dose is 15 mg/kg once weekly.

Group Type: EXPERIMENTAL

Iniparib (SAR240550-BSI-201)

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Iniparib/Gemcitibine/Carboplatin

Gemcitabine/carboplatin (GC) : Gemcitabine will be administered at 1,000 mg/m² as a 30min IV infusion and carboplatin area under the curve (AUC) 2 as a 60min IV infusion. Patients will receive gemcitabine/carboplatin infusions once weekly (days 1 and 8). Iniparib will be administered for two weeks, followed by a 1week of rest in a 21-day cycle (weekly schedule: days 1 and 8; twice weekly schedule: days: 1, 4, 8 and 11).

Group Type: EXPERIMENTAL

Iniparib (SAR240550-BSI-201)

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Gemcitabine

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Carboplatin

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Iniparib/Paclitaxel

Paclitaxel (P): Paclitaxel will be administered at the dose of 80 mg/m2 as a 60-minute intravenous infusion administered on days 1, 8, and 15 followed by a 1week of rest. Iniparib will be administered for three weeks, followed by 1week of rest in a 28-day cycle (weekly schedule: days 1, 8 and 15; twice weekly schedule: days 1, 4, 8, 11, 15 and 18).

Group Type: EXPERIMENTAL

Iniparib (SAR240550-BSI-201)

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Placlitaxel

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Iniparib/Pegylated liposomal doxorubicin/Carboplatin

Pegylated liposomal doxorubicin (Doxil)/Carboplatin (PLD) : Doxil will be administered at 30 mg/m² as a 30min IV infusion and carboplatin AUC 4 as a 60min IV infusion on day 1 every four weeks. Iniparib will be administered for two weeks in a 28-day cycle (weekly schedule: days 1, and 8; twice weekly schedule: days 1, 4, 8, and 11).

Group Type: EXPERIMENTAL

Iniparib (SAR240550-BSI-201)

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Carboplatin

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Pegylated liposomal doxorubicin

Intervention Type: DRUG

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Interventions

Iniparib (SAR240550-BSI-201)

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Intervention Type: DRUG

Gemcitabine

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Intervention Type: DRUG

Carboplatin

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Intervention Type: DRUG

Placlitaxel

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Intervention Type: DRUG

Pegylated liposomal doxorubicin

Pharmaceutical form:Solution for infusion

Route of administration: Intravenous

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Capable of understanding and complying with the protocol requirements, and have signed the informed consent document
• ≥18 years of age
• Eastern Cooperative Oncology Group (ECOG) performance status 0-1.
• To have histological or cytological evidence of a diagnosis of cancer that is advanced and/or metastatic disease; that is refractory to standard therapy and/or therapies known to provide clinical benefit or for which no standard therapy exists
• For phase 1b, patients for whom the backbone chemotherapy (dose and schedule) can be considered as a standard therapeutic regime for their cancer.
• Have measurable disease or non-measurable disease, defined according to RECIST Version 1.1. Patients with skin only metastases are eligible, if the appropriate photography documentation (including measurement) of the skin metastases is provided.
• Adequate organ and bone marrow function
• Willingness, if not postmenopausal or surgically sterile, to abstain from sexual intercourse or employ an effective barrier method of contraception during the study drug administration and for a period of 6 months following the last dose.
• Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to start of treatment. Women of childbearing potential or men with partners of childbearing potential must use effective birth control measures during treatment, and at least 6 months after the last dose of study treatment. If a woman becomes pregnant or suspects she is pregnant while participating in this study, she must agree to inform her treating physician immediately. Sexually active men must agree to use a medically acceptable form of birth control during treatment and at least 6 months after the last dose. If a female partner becomes pregnant during course of study the treating physician should be informed immediately.

Exclusion Criteria

• Systemic anticancer therapy within 14 days before the first dose of study drug.
• Known allergy or hypersensitivity to components of the iniparib, gemcitabine, paclitaxel, PLD,or carboplatin formulation.
• Not recovered to Grade ≤1 from adverse events (AE), per NCI-CTCAE Version 4.03 or to within 10% of pre-treatment baseline values, due to investigational drugs, radiation, or other medications administered more than 30 days before enrollment in this study. Alopecia at screening is not exclusionary.
• Prior radical (curative) radiation therapy for treatment of cancer ≥25% of the bone marrow (1). Prior radiation to the whole pelvis is not allowed. Prior radical radiotherapy must be completed at least 4 weeks before study entry.
• Patients who have received palliative radiation therapy for symptomatic metastases must have completed treatment ≥14 days prior to initiation of study treatment.
• Active brain metastases. Patients with treated brain metastases are eligible, if 1. Radiation therapy was completed at least 2 weeks prior to study treatment; 2. Follow-up scan shows no disease progression; and 3. Patient does not require steroids. Screening for brain metastases is not required if the patient is asymptomatic.
• Clinically significant cardiac disease including congestive heart failure (New York Heart Association Class III or IV), including pre-existing ventricular arrhythmia or conduction abnormality requiring medication, or cardiomyopathy or history of a myocardial infarction within the last 6 months
• Other major medical condition (eg, uncontrolled pulmonary, renal, or hepatic dysfunction, uncontrolled infection) which the Investigator feels might compromise the patient's effective and safe participation in the trial.
• Pregnant or breastfeeding
• Have known positive test results in human immunodeficiency virus (HIV), hepatitis B surface antigen (HBSAg), or Hepatitis C Antibodies (HCAb). Testing is not required unless circumstances warrant confirmation.
• Patients with acute or chronic leukemia or with any other disease likely to have a significant bone marrow infiltration (screening not required).
• Prior treatment with gemcitabine, carboplatin, paclitaxel, or Pegylated liposomal doxorubicin.

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Sciences & Operations

Role: STUDY_DIRECTOR

Sanofi

Locations

Investigational Site Number 840002

Scottsdale, Arizona, United States

Investigational Site Number 840004

Los Angeles, California, United States

Investigational Site Number 840010

Augusta, Georgia, United States

Investigational Site Number 840007

St Louis, Missouri, United States

Investigational Site Number 840001

Cincinnati, Ohio, United States

Investigational Site Number 840006

San Antonio, Texas, United States

Countries

United States

Other Identifiers

U1111-1118-6091

Identifier Type: OTHER

Identifier Source: secondary_id

TED11746

Identifier Type: -

Identifier Source: org_study_id