Sarah E S Leary, MD, MS

Dr. Sarah Leary, MD

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Seattle Children's Hospital

Expert in Brain Tumor
Expert in Brain Cancer
78 reported clinical trials
139 drugs studied

About Sarah Leary, MD

Education:

  • Earned an MD (Doctor of Medicine).
  • Holds an MS (Master of Science).

Experience:

  • Since August 2009, serves as Attending Physician and Medical Director of the Pediatric Brain Tumor Program at Seattle Children's Hospital.
  • Professor in the Department of Pediatrics at the University of Washington School of Medicine.
  • Medical Director of Clinical Research at the Ben Towne Center for Childhood Cancer Research.
  • Actively involved in national and international pediatric brain tumor research and data sharing initiatives.
  • Recognized as Seattle's Top Doctor in 2022 by Seattle Magazine.

Area of expertise

1Brain Tumor
Global Leader
Sarah Leary, MD has run 36 trials for Brain Tumor. Some of their research focus areas include:
NTRK positive
H3.3K27M positive
Stage IV
2Brain Cancer
Global Leader
Sarah Leary, MD has run 19 trials for Brain Cancer. Some of their research focus areas include:
Stage IV
Stage I
Stage II

Affiliated Hospitals

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Seattle Children's Hospital

Clinical Trials Sarah Leary, MD is currently running

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Selumetinib vs. Chemotherapy

for Brain Cancer

This trial is comparing a new drug, selumetinib, with standard chemotherapy to treat patients with a specific type of brain tumor. The patients do not have a certain genetic mutation and are not affected by a genetic disorder. Selumetinib works by blocking enzymes needed for tumor growth, while the standard drugs kill or stop tumor cells from dividing.
Recruiting2 awards Phase 3
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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

More about Sarah Leary, MD

Clinical Trial Related8 years of experience running clinical trials · Led 78 trials as a Principal Investigator · 30 Active Clinical Trials
Treatments Sarah Leary, MD has experience with
  • Cyclophosphamide
  • Radiation Therapy
  • Nivolumab
  • Etoposide
  • Cisplatin
  • Doxorubicin Hydrochloride

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