Solid Tumors or Mantle Cell Lymphoma Clinical Trial
Official title:
A Dose-Escalation Open-Label Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of CEP-9722 (a PARP 1 and PARP 2 Inhibitor) in Combination With Gemcitabine and Cisplatin in Patients With Advanced Solid Tumors or Mantle Cell Lymphoma
The primary objective of the study is to determine the maximum tolerated dose (MTD) of CEP-9722 in combination with gemcitabine and cisplatin in patients with advanced solid tumors or mantle cell lymphoma.
| Status | Completed |
| Enrollment | 24 |
| Est. completion date | January 2013 |
| Est. primary completion date | December 2012 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Written informed consent is obtained. The patient has a either a histologically or cytologically confirmed malignant advanced solid tumor or a mantle cell lymphoma (and has experienced failure of as least 1 previous therapy) and the patient may benefit from the combination of gemcitabine and cisplatin. - The patient has measurable or nonmeasurable disease evaluated according to Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 guidelines. - The patient is a man or woman at least 18 years of age. - The patient has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. - The patient has a life expectancy of 12 weeks or more. - The patient has adequate hematologic assessments and adequate renal and hepatic function as specified in the study protocol - The patient has audiogram results without clinically significant abnormalities. - The patient may have had chemotherapy provided that at least 3 weeks have elapsed and prior sequelae have resolved. If the patient has had prior radiation (curative or palliative) or prior treatment with nitrosoureas, a minimum of 4 weeks and 6 weeks, respectively, must have elapsed before treatment with CEP-9722. - The patient has had no immunotherapy, including monoclonal antibody therapy, for at least 4 weeks and no hormonal therapy for at least 1 week, with the exception of patients with prostate cancer, who may continue hormonal therapy. - Written informed consent is obtained. - Agreement by women of childbearing potential (not surgically sterile or 2 years postmenopausal) to use a medically accepted method of contraception and continue the use of this method for the duration of the study and for 90 days after participation in the study. Acceptable methods of contraception include abstinence, barrier method with spermicide, intrauterine device (IUD), or steroidal contraceptive (oral, transdermal, implanted, and injected) in conjunction with a barrier method. - Agreement by men not surgically sterile or who are capable of producing offspring to practice abstinence or use a barrier method of birth control, and continue use of this method for the duration of the study and for 6 months after participation in the study. Exclusion Criteria: - With the exception of cancer, the patient has any serious or uncontrolled surgical, medical, or psychiatric history that could prevent compliance with study procedures, or compromise the integrity of the study. - The patient has any of the protocol specified risk factors for Torsade de Pointes - The patient has a brain lesion requiring systemic therapy with corticosteroids or anti-convulsive agents. - The patient has previous hypersensitivity reactions to 1 or more of the components of the CEP-9722, gemcitabine, or cisplatin drug products. - The patient is a pregnant or breast-feeding woman. (Any women becoming pregnant during the study will be withdrawn from the study.) - The patient is participating in another interventional clinical study at the time of enrollment or has participated in another interventional clinical study within 4 weeks prior to enrollment. - The patient has any malabsorption syndrome and/or prior gastrectomy - The patient has a concomitant uncontrolled and/or chronic infection or severe systemic disease. - The patient has had previous treatment with another poly (adenosine diphosphate-ribose) polymerase (PARP) inhibitor. - The patient is unable to swallow tablets. - The patient cannot interrupt continuous treatment with proton pump inhibitors and/or H2 receptor antagonists. |
Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Belgium | Teva Investigational Site 3 | Bruxelles | |
| France | Teva Investigational Site 1 | Nantes | |
| France | Teva Investigational Site 2 | Villejuif |
| Lead Sponsor | Collaborator |
|---|---|
| Cephalon |
Belgium, France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Determination of the maximum tolerated dose (MTD) of CEP-9722 in combination with gemcitabine and cisplatin in patients with advanced solid tumors or mantle cell lymphoma. | To determine the maximum tolerated dose of CEP-9722, as defined by dose-limiting toxicities (DLTs) reported during the second 21-day treatment cycle (the first cycle of CEP-9722 administration). | Baseline and endpoint (as soon as possible after Day 21 of the last cycle) | Yes |
| Secondary | Evaluate the safety and tolerability of CEP-9722 in combination with gemcitabine and cisplatin | Assessed by the occurrence of adverse events, clinical laboratory test results, vital signs measurements, electrocardiogram (ECG) findings, physical examination findings, and concomitant medication usage. Creatinine clearance will be calculated according to the Cockroft-Gault formula. An audiogram will be performed at screening and repeated during the study if clinically relevant according to the investigator. Pts who complete or withdraw from treatment will have final procedures/assessments performed as soon as possible, after day 21 of the last cycle, at the end-of-treatment visit. | During the entire study, a minimum of 6 wks (two 21-day cycles) up to a maximum of 18 wks (six 21-day cycles). | Yes |
| Secondary | Cmax pharmacokinetics parameter | To characterize the pharmacokinetics profile of CEP-8983 (the active moiety of CEP-9722) following administration of CEP-9722, through measurement of the Maximum observed drug Concentration (Cmax). | Days 2 and 7 of Cycle 2 and Day 7 of Cycle 3 | No |
| Secondary | AUC pharmacokinetics parameter | To characterize the pharmacokinetics profile of CEP-8983 (the active moiety of CEP-9722) following administration of CEP-9722, through measurement of the Area Under the plasma concentration-time Curve (AUC). | Days 2 and 7 of Cycle 2 and Day 7 of Cycle 3 | No |
| Secondary | Pharmacodynamics assessment | To determine the extent of poly-adenosine diphosphate ribose polymerase (PARP) inhibition in peripheral blood mononuclear cells following administration of CEP-9722 | Screening and Day 2 of Cycle 2 at predose, and at 2 and 6 hours after administration of CEP-9722 | No |
| Secondary | Efficacy - will be assessed by Tumor response evaluation of each patient | Tumor response will be determined using the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 guidelines, when possible for patients with solid tumors. For patients with mantle tumors, tumor response may be evaluated by the International Working Group criteria. | Screening, cycles 3 and 6, and every 2 cycles after cycle 6 until disease progression | No |