Index of Current Clinical Trials
Listed below are study summaries
of the clinical trials SDCRI is presently
supporting. (Programs for prostate cancer and brain tumors
are under development).
- Breast
Cancer
- Colorectal Cancer
- Low Grade Non-Hodgkin's
Lymphoma
- Non-Small Cell Lung Cancer
(NSCLC)
- Prostate
Cancer
Low Grade Non-Hodgkin's Lymphoma
1. A Phase II Open-Label Research
Study Using Standard Therapy in Combination with a Tumor Specific
Immunotherapy
Target Patient Population:
· Low Grade Non-Hodgkin's Lymphoma (NHL)
· Patients may have receive 0 to 2 prior therapies
for their disease
· Patients must have a site of disease that is accessible
for biopsy.
· Patients must not be resistant to Rituxan
The patient will have a vaccine-like
therapy developed from their own tumor tissue that will be
used to create an immunotherapy. This Tumor Specific immunotherapy
will be used in combination with standard treatment.
Please contact Christine DeFrancisco
at 760-598-1700 for more details.
2. A Phase IV Open-Label Research
Study Using Standard Chemotherapy in Combination with Rituxan
Target Patient Population:
· Low Grade Non-Hodgkin's Lymphoma (NHL)
· Patients must have not had previous treatment for
NHL
· Patients must be eligible for chemotherapy
· Patients must have stage 3 or 4 disease
The patient will have standard chemotherapy
in combination with Rituxan treatment for a total of approximately
5 months followed by Rituxan maintenance treatment for a total
of 2 years.
Please contact Christine DeFrancisco
at 760-598-1700 for more details.
3. A Phase IV Open-Label Research
Study Using Standard Chemotherapy in Combination with Rituxan
Target Patient Population:
· Diffuse Large Cell or Follicular Center Cell Non-Hodgkin's
Lymphoma (NHL)
· Patients must have not had previous treatment for
NHL
· Patients must be eligible for chemotherapy
· Patients must have Stage II Bulky Disease, Stage
3 or Stage 4
The patient will have standard chemotherapy
in combination with Rituxan treatment for a total of approximately
5 months followed by Rituxan maintenance treatment for a total
of 2 years.
Please contact Christine DeFrancisco
at 760-598-1700 for more details.
4. A Phase II Trial using a Novel
Agent Plus Rituxan
Target Patient Population:
· Patients must have recurrent or refractory low-grade
CD20+ B-Cell Non-Hodgkin's Lymphoma (NHL) with measurable
disease confirmed by CT scan.
· Patients must have received one prior chemotherapy
regimen for NHL
· Patients may not have received prior antibody therapy
for lymphoma (other than Rituxan)
· Patients may not have known HACA/HAHA positivity.
The patient will receive a novel agent
in combination with weekly Rituxan. This is an open-label,
non-randomized research study, therefore all patients receive
the same treatment and know the treatment they are receiving.
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