First in Man Study of SAR566658 Administered in Patients With CA6-Positive and Refractory Solid Tumor

NCT ID: NCT01156870

Last Updated: 2017-05-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 114 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-09-08
• Study Completion Date: 2017-04-07

Brief Summary

Primary Objective:

To determine the maximum tolerated dose (MTD) of SAR566658

Secondary Objectives:

• To characterize the safety profile of SAR566658
• To evaluate the pharmacokinetic profile of SAR566658
• To assess the potential immunogenicity of SAR566658
• To assess preliminary antitumor activity
• To assess the effect of SAR566658 at recommended dose on CYP3A enzyme activity using midazolam
• To assess safety in the alternative schedules of SAR566658 administration

Detailed Description

The duration of the study for one patient in the dose escalation phase of the study will include a screening period of up to 3 weeks, a 3-week treatment cycle(s) and a 2-week treatment cycle(s). The patients may continue treatment until disease progression, unacceptable toxicity, or willingness to stop, followed by a minimum of 30-day follow-up. If a patient treated in dose escalation part or in an expansion cohorts, continues to benefit from the treatment at the time of Clinical Study Report, the patient can continue study treatment and will continue to undergo all assessments as per the study flowchart. Such patients will be followed at least until 30 days after the last IMP administration.

Conditions

Neoplasm Malignant

Study Design

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

Study Groups

SAR566658

SAR566658 will be administered by intravenous (IV) infusion according to three different schedules

Group Type: EXPERIMENTAL

SAR566658

Intervention Type: DRUG

Pharmaceutical form:solution for infusion

Route of administration: intravenous

Interventions

SAR566658

Pharmaceutical form:solution for infusion

Route of administration: intravenous

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Diagnosis of CA6-positive solid tumors as moderate to intense membrane staining of ≥15% of tumor cells for which no standard therapy is available.

Exclusion Criteria

• Eastem Cooperative Oncology Group performance status ≥2.
• Any serious active disease or co-morbid condition, which, in the opinion of the Investigator, may interfere with the safety or the compliance with the study.
• Poor bone marrow reserve.
• Poor liver and renal function.
• Pregnant or breast-feeding woman.
• No use of effective birth control methods, when applicable.
• No resolution of all specific toxicities (excluding alopecia) related to any prior anti-cancer therapy to Grade ≤1 according to the National Cancer Institute - Common Toxicity Criteria for Adverse Events (NCI-CTCAE) version 4.03 grade scaling.
• Wash out period of less than 3 weeks from previous antitumor therapy or any investigational treatment, (and less than 6 weeks in case of prior nitroso-urea and or mitomycin C treatment). Patients will be eligible if hormonotherapy (ie, for breast tumors) is discontinued before first Investigational product administration.
• Wash out period of less than 1 week from last palliative dose of radiotherapy.
• Patients with respiratory insufficiency defined by a decrease more than 50% compared to theoretical baseline pulmonary volumes and theoretical baseline Diffusing capacity of the Lung for Carbon monoxyde.
• Any lung radiotherapy in patient's cancer history.
• Patients with previous history or active interstitial lung disease or pulmonary fibrosis.
• Patients with abnormal cardiac function defined by a Left Ventricular Ejection Fraction <50%.
• Patients with previous history of acute cardiac failure.
• Patients with previous history and/or unresolved corneal disorders.
• Known intolerance to infused protein products or maytansinoids.
• Patients treated with strong CYP3A inhibitors within 2 weeks prior study drug administration.
• For patients to be treated in the midazolam cohort:
• Any treatment known to induce CYP3A isoenzymes or to inhibit CYP3A4 activities not allowed within 2 weeks before midazolam administration and up to the end of pharmacokinetic sampling following the last midazolam administration.
• Any contra-indications to midazolam, according to the applicable labeling.
• Patients older than 60 years.

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

Cincinnati, Ohio, United States

Investigational Site Number 840001

San Antonio, Texas, United States

Investigational Site Number 250001

Toulouse, , France

Investigational Site Number 724002

Madrid, , Spain

Investigational Site Number 724001

Madrid, , Spain

Countries

United States; France; Spain

Other Identifiers

U1111-1116-4129

Identifier Type: OTHER

Identifier Source: secondary_id

TED10499

Identifier Type: -

Identifier Source: org_study_id