Safety and Pharmacokinetics of SAR245408 Daily Oral in Patients With Solid Tumors

NCT ID: NCT01392924

Last Updated: 2014-12-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-08-31
• Study Completion Date: 2014-11-30

Brief Summary

Primary Objective:

• To confirm safety and tolerability of global recommended phase three dose (RPTD) of SAR245408 tablets when administered on continuous once daily dosing (CDD) in patients with solid tumors.

Secondary Objectives:

• To evaluate the plasma pharmacokinetics (PK) of daily oral administration of SAR245408 in CDD treatment schedule in patients with solid tumors.
• To gather preliminary efficacy data after repeated administration of SAR245408 in patients with solid tumors.

Detailed Description

The duration of the study for 1 patient will include a period for screening up to 28 days, the study treatment period, followed by a 28-day follow-up after the last study drug administration.

Conditions

Neoplasm Malignant

Study Design

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

Study Groups

SAR245408

single cohort: SAR245408 administered once daily

Group Type: EXPERIMENTAL

SAR245408

Intervention Type: DRUG

Pharmaceutical form: tablet Route of administration: oral

Interventions

SAR245408

Pharmaceutical form: tablet Route of administration: oral

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically confirmed solid tumor that is metastatic or unresectable, and for which standard curative or palliative measures do not exist or are no longer effective, and there are no known therapies to prolong survival.
• Before any study-specific procedure, the appropriate Institutional Review Board (IRB) approved written informed consent must be obtained. Second informed consent must be obtained before the patient starts the Treatment Extension Period (Cycle 2 and after).

Measurable disease as per Response Evaluation Criteria in Solid Tumors (RECIST) criteria.

Exclusion Criteria

• < 20 years old.
• Eastern Cooperative Oncology Group (ECOG) performance status > 2.
• Incapable of understanding or complying with the protocol or has not signed the informed consent document.
• Unable or unwilling to abide by the study protocol or cooperate fully with the investigator or designee.
• Inadequate organ or bone marrow function.
• Prothrombin time (PT)/International Normalized Ratio (INR) and/or partial thromboplastin time (PTT) test results at screening that are above 1.3 × the laboratory upper limit of normal (ULN).
• Baseline corrected QT interval (QTc) > 460 ms.
• Sexually active (males and females) who do not agree to use medically acceptable methods of contraception during the course of the study and for 3 months following discontinuation of study drug. Female patients of childbearing potential must have a negative pregnancy test at screening.
• Pregnant or breastfeeding.
• Has not tolerated previous treatment with other phosphatidylinositol 3-kinase (PI3K) inhibitor, or has been treated with SAR245408.
• Not recovered from all previous therapies (i.e. radiation, surgery, or medication)
• Currently receiving anticoagulation with therapeutic doses of warfarin (low-dose warfarin ≤ 1mg/day is permitted).
• Primary brain tumor or brain metastasis are considered eligible if the patient has not received radiation therapy for brain metastasis within 2 weeks of enrollment and has been on a stable dose of steroids for 2 or more weeks.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection (including cytomegalovirus, Epstein-Barr virus, toxoplasmosis, and hepatitis B and C), symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.
• Known to be positive for the human immunodeficiency virus (HIV)
• Psychiatric illness/social situation(s) that would limit compliance with study requirements.
• Allergy or hypersensitivity to components of the SAR245408 formulation.
• Withdraws consent during the screening (starting from signed informed consent form (ICF))
• Patient who is judged by the investigator as not suitable for participating in the study

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

• Minimum Eligible Age: 20 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 392002

Kobe, , Japan

Investigational Site Number 392001

Nagoya, , Japan

Countries

Japan

Other Identifiers

U1111-1118-9727

Identifier Type: OTHER

Identifier Source: secondary_id

TED11883

Identifier Type: -

Identifier Source: org_study_id