A Study to Evaluate the Effects of Combining Cabazitaxel With Cisplatin Given Every 3 Weeks in Patients With Advanced Solid Cancer
| Status: | Completed |
|---|---|
| Conditions: | Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 3/30/2013 |
| Start Date: | June 2009 |
| End Date: | March 2013 |
| Contact: | For site information, send an email with site number to |
| Email: | Contact-Us@sanofi.com |
A Dose-Escalation Study Of The Safety, Tolerability, And Pharmacokinetics Of Cabazitaxel In Combination With Cisplatin Administered Every 3 Weeks In Subjects With Advanced Solid Malignancies
This study is designed as a phase 1, multicenter, open-label, single arm, dose-escalation,
study of Cabazitaxel in combination with cisplatin, to determine safety, pharmacokinetics
(PK), and efficacy in solid tumors (parts 1 and 2) and single sequence, two-treatment,
crossover studies to determine the effect of strong CYP3A4 inhibition and induction on the
PK of Cabazitaxel in patients with solid tumors (part 3 and part 4, respectively).
There are 4 parts to the study:
Part 1: Determine the Dose Limiting Toxicities (DLT)'s and Maximum Tolerated Dose (MTD)
based on safety.
Part 2: Determine the anti-tumor activity of the combination regimen at the Maximum
Tolerated Dose (MTD) in an extended cohort of patients.
Part 3: Determine the effect of a strong CYP3A4 inhibitor (ketoconazole) on the
pharmacokinetic (PK) of Cabazitaxel.
Part 4: Determine the effect of a strong CYP3A4 inducer (rifampin) on the pharmacokinetic
(PK) of Cabazitaxel.
The total duration on the study per subject will be about 26 weeks broken down as follows:
- A maximum of 21-day screening phase,
- 21-days (+/- 2 weeks) study treatment cycles,
- 30-day follow-up visit after the last dose of study medication.
- Cut-off date for parts 1, 2, 3 and 4: when the last patient has completed 6 cycles
(parts 1 and 2) or 2 cycles (parts 3 and 4) of treatment or discontinued study
treatment (for disease progression, unacceptable toxicity, withdrawal of consent, or
investigator's decision to withdraw), whichever comes first, in the corresponding part.
Patients still receiving treatment at the cut-off date may continue to receive treatment
beyond the cut-off date at investigator's discretion if benefiting.
Inclusion criteria:
- confirmed metastatic or unremovable advanced solid malignancy that is metastatic or
unresectable, and for which standard curative measures do not exist, but for which
cisplatin based therapy is appropriate
- signed informed consent
Exclusion criteria
- limited physical functioning (as evaluated by the Eastern Cooperative Oncology Group
(ECOG) scale)
- inability to follow study requirements and schedule
- treatment of cancer within 3 weeks of study, concurrent treatment in another clinical
trial or with any other cancer therapy
- serious medical illness at same time of study and/or significantly abnormal lab
reports
- lack of pregnancy contraception (women of childbearing potential), pregnancy, or
breast feeding.
- Women of childbearing potential not protected by highly effective contraceptive
method of birth control OTHER than hormonal contraception (Part 4 only).
- prior significant hearing or kidney problems
- continued toxic effects of prior chemotherapy
- cancers that cannot be physically measured (Part 2 only)
The above information is not intended to contain all considerations relevant to a
patient's potential participation in a clinical trial.
We found this trial at
8
sites
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