Efficacy and Safety of Oral CEP-701 for the Treatment of Patients With Advanced Multiple Myeloma

Cephalon

Status and phase

Terminated

Phase 2

Conditions

Myeloma

Treatments

Drug: Oral CEP-701

Study type

Interventional

Funder types

Industry

Identifiers

C0701/2025/ON/US

Details and patient eligibility

About

An Open-Label Study of the Efficacy and Safety of Oral CEP-701 for the Treatment of Patients with Advanced Multiple Myeloma.

Full description

An Open-Label Study of the Efficacy and Safety of Oral CEP-701 for the Treatment of Patients with Advanced Multiple Myeloma.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients are included in the study if all of the following criteria are met:

Histological and cytological confirmation of stage II or III multiple myeloma.
Relapsed or primary refractory multiple myeloma, after 1 or more courses of standard therapy, and progressive disease.
ECOG performance status of 0-1.
Measurable disease as defined by serum M protein of more than 1.0 gm/dl, serum light chain of more than 200 mg/dL, or Bence-Jones proteinuria of more than 200mg/24 hours.
At least 18 years of age.
Normal marrow function: ANC>1.0x10 9/L, platelets>50X10 9/L An exception is allowed if myelosuppression or thrombocytopenia is secondary to bone marrow plasmacytosis. Growth factor support is allowed.
Normal organ function: bilirubin <1.5XULN, AST and ALT<2XULN, serum creatinine <2.0 mg/dL.
Contraceptive measures during participation as appropriate.
Willing to be able to comply with study procedures and restrictions.
Signed written informed consent.

Exclusion criteria

Patients are excluded from participating in this study if 1 or more of the following criteria are met:

Nonsecretory disease or plasma cell leukemia (defined as >2000 circulating plasma cells/uL).
More than 4 prior courses if anticancer therapy (bisphosphonates are not considered anticancer therapy for this criterion)
Chemotherapy or radiotherapy within 4 weeks prior to enrollment
Unresolved adverse events or uncontrolled illness that would be likely to interfere with the objectives of the study.
Treatment with an investigational drug within 4 weeks of first day of study treatment
History of second cancer (except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease free more than 5 years).
Treatment with potent CYP3A4 inhibitors including cyclosporine, clotrimazole, fluconazole, itraconazole, ketoconazole, voriconazole, erythromycin, clarithromycin, and troleandomycin, human immunodeficiency virus (HIV), protease inhibitors, or nefazodone within 1 week (7 days) of the planned 1st day of study treatment.
Currently receiving warfarin.
Clinical diagnosis of active gastrointestinal ulceration of melena or hematemesis in the previous 4 weeks.
Hypersensitivity to CEP701 or any component of CEP701.
Intolerance of dexamethasone.
Requirement for HIV protease inhibitor treatment.