A Single Arm, Multicenter, Phase II Trial of RAD001 as Monotherapy in the Palliative Treatment of Patients With TCC After Failure of Chemotherapy

NCT ID: NCT00714025

Last Updated: 2012-01-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-11-30
• Study Completion Date: 2012-01-31

Brief Summary

An open-label, single arm, non-randomized, single stage phase II study. 3 phases:Baseline, treatment/duration and Follow-up. All patients will be treated with RAD001 10 mg daily dose until disease progression or unacceptable toxicity death, or discontinuation from the study, for any other reason

Detailed Description

An open-label, single arm, non-randomized, single stage phase II study. Baseline phase: Baseline evaluations will be performed within 2 weeks before the first dose study drug.

Treatment phase/duration of treatment: All patients will be treated with RAD001 10mg PO daily dose until disease progression (by RECIST) or unacceptable toxicity death or discontinuation from the study for any other reason.

Follow-up phase: All patients will have a follow-up visit scheduled 28 days after the last dose of the study drug to follow for AEs and SAEs that may have occured after discontinuation from the study. Any patient who is discontinued from treatment with RAD001 for any reason other than disease progression will continue to have tumor assessments until the patient has documented disease progression or start of additional anti-tumor therapy. Central radiology review and survival data collection will be performed. After discontinuation of RAD001 all patients will be followed up for survival until the final OS analysis is performed.

Conditions

Transitional Cell Carcinoma

Study Design

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

Study Groups

I

40 patients with metastatic or locally advanced transitional bladder cancer with failed platinum-based chemotherapy receiving RAD001 10mg daily PO.

Group Type: EXPERIMENTAL

RAD001

Intervention Type: DRUG

RAD001 10mg, daily, PO

Interventions

RAD001

RAD001 10mg, daily, PO

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients histologically-or cytologically-confirmed locally advanced or metastatic TCC not amenable to curative surgery or radiation.
• Patients with documented disease progression after first-line platinum based therapy
• an interval of more than 4 weeks since last cytotoxic chemotherapy, biological therapy, surgery or radiotherapy
• patients with at least one measurable lesion as at baseline as per RECIST criteria
• ECOG performance status of 0-2
• Adequate bone marrow function
• Adequate liver function
• Adequate renal function
• Life expectancy more than 3 months
• Women of child-bearing age must have a negative pregnancy test within 72 hours prior to the administration of the study treatment start
• Signed informed consent prior to beginning protocol specific procedure
• Age more than 18 years old

Exclusion Criteria

• Patients who have received more than 2 systemic treatment for their metastatic disease
• Patients who have previously received mTOR inhibitors
• Patients with a know hypersensitivity to RAD001 or other rapamycin or to its recipients
• Patients with brain or leptomeningeal metastases
• Patients receiving chronic systemic treatment with corticosteroids or another immunosuppressive agent
• Patients with a known history of HIV seropositivity
• Patients with autoimmune hepatitis
• patients with an active, bleeding diathesis
• Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study
• Patients who have a history of another primary malignancy more than 5 years
• Patients who are using other investigational agents or who had received investigational drugs more than 4 weeks prior to study treatment start
• Patients unwilling to or unable to comply with the protocol
• Female patients who are pregnant or breast feeding, or adults of reproductive potential who are not using effective birth control methods. If barrier contraceptives are being used, these must be continued throughout the trial by both sexes. Oral contraceptives are not acceptable.

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

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jean-Pascal H Machiels, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Cliniques Universitaires St Luc-UCL

Locations

Cliniques Universitaires St Luc-UCL

Brussels, , Belgium

Countries

Belgium

Other Identifiers

UCL-ONCO 08-002

Identifier Type: -

Identifier Source: org_study_id