Rabi Hanna, MD | Cleveland Clinic

Dr. Rabi Hanna

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Cleveland Clinic Foundation

Expert in Cancer
Studies Brain Tumor
51 reported clinical trials
118 drugs studied

About Rabi Hanna

Education:

  • Obtained MD from Aleppo University Faculty of Medicine, Aleppo, Syria.

Experience:

  • Board certified in Pediatrics and Pediatric Hematology-Oncology.
  • Completed Pediatric residency at Duke University Medical Center, Durham, North Carolina.
  • Undertook Pediatric hematology-oncology fellowship at Fred Hutchinson Cancer Research Center and Seattle Children's Hospital, Washington.
  • Director of Pediatric Bone Marrow Transplantation at Cleveland Clinic Children's Hospital.
  • Specializes in leukemia, lymphoma, solid tumors, and inherited non-malignant disorders treatment.

Area of expertise

1Cancer
Global Leader
Rabi Hanna has run 12 trials for Cancer. Some of their research focus areas include:
Stage I
Stage IV
Stage II
2Brain Tumor
Rabi Hanna has run 9 trials for Brain Tumor. Some of their research focus areas include:
Stage IV
NTRK1 positive
NTRK positive

Affiliated Hospitals

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Cleveland Clinic Foundation
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Cleveland Clinic

Clinical Trials Rabi Hanna is currently running

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Inotuzumab Ozogamicin

for Acute Lymphoblastic Leukemia

This phase III trial studies whether inotuzumab ozogamicin added to post-induction chemotherapy for patients with High-Risk B-cell Acute Lymphoblastic Leukemia (B-ALL) improves outcomes. 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. Inotuzumab ozogamicin is a monoclonal antibody, called inotuzumab, linked to a type of chemotherapy called calicheamicin. Inotuzumab attaches to cancer cells in a targeted way and delivers calicheamicin 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. This trial will also study the outcomes of patients with mixed phenotype acute leukemia (MPAL) and disseminated B lymphoblastic lymphoma (B-LLy) when treated with high-risk ALL chemotherapy. The overall goal of this study is to understand if adding inotuzumab ozogamicin to standard of care chemotherapy maintains or improves outcomes in High Risk B-cell Acute Lymphoblastic Leukemia (HR B-ALL). The first part of the study includes the first two phases of therapy: Induction and Consolidation. This part will collect information on the leukemia, as well as the effects of the initial treatment, to classify patients into post-consolidation treatment groups. On the second part of this study, patients with HR B-ALL will receive the remainder of the chemotherapy cycles (interim maintenance I, delayed intensification, interim maintenance II, maintenance), with some patients randomized to receive inotuzumab. The patients that receive inotuzumab will not receive part of delayed intensification. Other aims of this study include investigating whether treating both males and females with the same duration of chemotherapy maintains outcomes for males who have previously been treated for an additional year compared to girls, as well as to evaluate the best ways to help patients adhere to oral chemotherapy regimens. 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.
Recruiting2 awards Phase 3
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T Cell-Depleted Stem Cell Transplant

for Leukemia

This phase II trial studies how well naive T-cell depletion works in preventing chronic graft-versus-host disease in children and young adults with blood cancers undergoing donor stem cell transplant. Sometimes the transplanted white blood cells from a donor attack the body's normal tissues (called graft versus host disease). Removing a particular type of T cell (naive T cells) from the donor cells before the transplant may stop this from happening.
Recruiting1 award Phase 222 criteria

More about Rabi Hanna

Clinical Trial Related8 years of experience running clinical trials · Led 51 trials as a Principal Investigator · 16 Active Clinical Trials
Treatments Rabi Hanna has experience with
  • Cyclophosphamide
  • Methotrexate
  • Radiation Therapy
  • Etoposide
  • Doxorubicin Hydrochloride
  • Vincristine Sulfate

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