Dana B. Salzberg, MD | Phoenix Children ...

Dr. Dana Salzberg

Claim this profile

Phoenix Childrens Hospital

Studies Burkitt's Leukemia
Studies Acute Lymphoblastic Leukemia
13 reported clinical trials
38 drugs studied

Area of expertise

1

Burkitt's Leukemia

Dana Salzberg has run 6 trials for Burkitt's Leukemia. Some of their research focus areas include:

Philadelphia chromosome positive
BCR-ABL1 fusion positive
ABL-class fusion positive
2

Acute Lymphoblastic Leukemia

Dana Salzberg has run 6 trials for Acute Lymphoblastic Leukemia. Some of their research focus areas include:

CD19 positive
BCR-ABL1 fusion positive
ABL-class fusion positive

Affiliated Hospitals

Image of trial facility.

Phoenix Children's Hospital

Clinical Trials Dana Salzberg is currently running

Image of trial facility.

Inotuzumab Ozogamicin

for Acute Lymphoblastic Leukemia

This phase III trial studies whether inotuzumab ozogamicin added to post-induction chemotherapy and immunotherapy (chemo-immunotherapy) for patients with High-Risk B-cell Acute Lymphoblastic Leukemia (B-ALL) improves outcomes. Inotuzumab ozogamicin is a monoclonal antibody, which is a type of protein that can bind to certain targets on the surface of cells. Inotuzumab ozogamicin is a monoclonal antibody that is linked to a type of chemotherapy called calicheamicin. Inotuzumab attaches to cancer cells by binding to the CD22 protein on the surface of the cancer cell and delivering calicheamicin inside the cells to kill them. Other drugs used in the chemotherapy regimen, such as cyclophosphamide, cytarabine, dexamethasone, doxorubicin, daunorubicin, methotrexate, leucovorin, mercaptopurine, prednisone, thioguanine, vincristine, and pegaspargase or calaspargase pegol work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Blinatumomab is a specialized type of monoclonal antibody known as a bispecific T-cell engager (BiTE). It works by simultaneously binding to CD19 on cancer cells and CD3 on normal immune cells, bringing them together to destroy leukemia cells. Blinatumomab is a standard part of chemo-immunotherapy treatment for B-ALL. This trial also studies the outcomes of patients with mixed phenotype acute leukemia (MPAL), and B-lymphoblastic lymphoma (B-LLy) when treated with ALL therapy without inotuzumab ozogamicin or blinatumomab. The overall goal of this study is to understand if adding inotuzumab ozogamicin to standard of care chemo-immunotherapy maintains or improves outcomes in High Risk B-cell Acute Lymphoblastic Leukemia (HR B-ALL). The first part of the study includes the first phase of therapy: Induction. This part will collect information on the leukemia, as well as the effects of the initial treatment, to classify patients into post-induction treatment groups. On the second part of this study, patients with HR B-ALL will receive the remainder of the chemotherapy cycles (consolidation, blinatumomab block 1, interim maintenance 1, blinatumomab block 2, delayed intensification, interim maintenance 2, maintenance), with some patients randomized to receive inotuzumab. The patients that receive inotuzumab will not receive part of consolidation or part of delayed intensification. Other aims of this study include evaluating 1) side effects of treatment using patient-reported outcomes and health-related quality of life, 2) the best ways to help patients adhere to oral chemotherapy regimens, 3) the relationship between levels of inotuzumab ozogamicin in the blood and side effects, 4) the impact of chemo-immunotherapy on the immune system and risk of infection, and 5) the impact of social determinants of health on outcomes. Finally, this study will be the first to track the outcomes of subjects with disseminated B-cell Lymphoblastic Leukemia (B-LLy) or Mixed Phenotype Acute Leukemia (MPAL) when treated with B-ALL chemotherapy.

Recruiting

2 awards

Phase 3

Image of trial facility.

Non-TBI Conditioning

for HCT in Acute Lymphoblastic Leukemia

This study will evaluate the use of non- TBI (total body irradiation) conditioning for B-ALL patients with low risk of relapse as defined by absence of NGS-MRD (next generation sequencing minimal residual disease) before receiving a hematopoietic cell transplant (HCT). Patients diagnosed with B-ALL who are candidates for HCT will be screened by NGS-MRD on a test of bone marrow done before the HCT. Subjects who are pre-HCT NGS-MRD negative will be eligible to receive a non-TBI conditioning regimen as part of the treatment cohort of the study. Subjects who are pre-HCT NGS-MRD positive will be treated as per treating center standard and will be followed in an observational cohort (HCT center standard of care).

Recruiting

1 award

Phase 2

More about Dana Salzberg

Clinical Trial Related

6 years of experience running clinical trials · Led 13 trials as a Principal Investigator · 5 Active Clinical Trials

Treatments Dana Salzberg has experience with

  • Daunorubicin Hydrochloride
  • Cytarabine
  • Thioguanine
  • Cyclophosphamide
  • Prednisolone
  • Methotrexate

Other Doctors you might be interested in

Frequently asked questions

Do I need insurance to participate in a trial?

What does Dana Salzberg specialize in?

Is Dana Salzberg currently recruiting for clinical trials?

Are there any treatments that Dana Salzberg has studied deeply?

What is the best way to schedule an appointment with Dana Salzberg?

What is the office address of Dana Salzberg?

Is there any support for travel costs?