Cefuroxime Sodium Injection |
Kefurox; Zinacef |
Clinical Trial: Genasense™ (Oblimersen Sodium), Fludarabine, and Rituximab in Subjects with Chronic Lymphocytic Leukemia
This study is currently recruiting patients.
|
Purpose
The treatment combination of Rituxan® (rituximab) and fludarabine has previously been reported to produce a high percentage of responses with less toxicity than other combination treatments. However, some leukemia subjects continue to have leukemia despite treatment with these standard anticancer drug therapies, or they may work for only a short period of time. In some subjects, when the leukemia does not respond well to therapy the leukemia cells may be over-producing one or more proteins. One of these proteins is called Bcl-2. Bcl-2 is a protein that appears to protect cancer cells from being killed and thus lengthens the life of the cancer cells. GenasenseTM (oblimersen sodium) is a compound that blocks production of the Bcl-2 protein. By first lowering levels of Bcl-2, it is possible that chemotherapy drugs may work more effectively as a cancer treatment. Genasense may also directly kill CLL cells. This study will test whether treating subjects with Genasense, fludarabine and rituximab is safe and effective.
| Condition | Treatment or Intervention |
|---|---|
| Chronic Lymphocytic Leukemia | Drug: Oblimerson sodium, G3139 Drug: Fludarabine Drug: Rituximab |
MedlinePlus related topics: Leukemia, Adult Acute; Leukemia, Adult Chronic; Leukemia, Childhood
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Official Title: A Pilot Study of Genasense™ (Oblimersen Sodium, Bcl-2 Antisense Oligonucleotide), Fludarabine and Rituximab in Previously Treated and Untreated Subjects with Chronic Lymphocytic Leukemia
Expected Total Enrollment: 80
Study start: November 2003
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
Key Inclusion Criteria:
- Absolute lymphocyte count of > 10,000 cells/mm3 for untreated subjects. Previously treated subjects must have a history of an absolute count of > 10,000 cells/mm3
- Platelets > 50,000 cells/mm3
- Creatinine < 1.5 mg/dL
Key Exclusion Criteria:
- Less than 3 weeks from any prior major surgery or other surgery including radiation therapy, chemotherapy, immunotherapy, high-dose steroid therapy, cytokine, biologic or vaccine therapy for those subjects who were previously treated.
- History of autoimmune hemolytic anemia
- Prior allogeneic transplant
Location and Contact Information
District of Columbia
Georgetown University Medical Center/Lombardi Cancer Center, Washington, District of Columbia, 20007, United States; Recruiting
Blanche Mavromatis, Principal Investigator
New York
Long Island Jewish Medical Center, New Hyde Park, New York, 11040, United States; Recruiting
Kanti Rai, M.D., Principal Investigator
Roswell Park Cancer Institute, Buffalo, New York, 14263, United States; Recruiting
Asher Chanan-Khan, M.D., Principal Investigator
More Information
Genta's website
Record last reviewed: February 2004
Last Updated: October 13, 2004
Record first received: February 20, 2004
ClinicalTrials.gov Identifier: NCT00078234
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Cefuroxime Sodium Injection (Drug Digest)
- Kefurox (Drug Digest)

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