Dr. Jamal G. Misleh, MD - Newark, DE ...

Dr. Jamal Misleh, MD

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Medical Oncology Hematology Consultants, PA

Expert in Breast Cancer
Studies Pancreatic Cancer
28 reported clinical trials
48 drugs studied

About Jamal Misleh, MD

Education:

  • Obtained MD from the University of Miami School of Medicine in 2003.

Experience:

  • Completed an Internal Medicine Internship (2003-2004) and Residency (2004-2006) at the Hospital of the University of Pennsylvania.
  • Undertook a Fellowship in Hematology/Medical Oncology at the University of Maryland Medical Center (2006-2009).
  • Board Certified in Hematology and Medical Oncology by the American Board of Internal Medicine since 2009.
  • Affiliated with Medical Oncology Hematology Consultants, PA, and serves as the Director of US Oncology Network Clinical Trials.

Area of expertise

1

Breast Cancer

Global Leader

Jamal Misleh, MD has run 11 trials for Breast Cancer. Some of their research focus areas include:

Stage IV
Stage III
HER2
2

Pancreatic Cancer

Jamal Misleh, MD has run 7 trials for Pancreatic Cancer. Some of their research focus areas include:

Stage IV
NRG1 positive
Stage III

Affiliated Hospitals

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Christiana Care Health Services

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Medical Oncology Hematology Consultants PA

Clinical Trials Jamal Misleh, MD is currently running

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Genomic Testing

for Breast Cancer

The FLEX Registry will be implemented to operate as a large-scale, population based, prospective registry. All patients with stage I to III breast cancer who receive MammaPrint® and BluePrint testing on a primary breast tumor are eligible for entry into the FLEX Registry, which is intended to enable additional study arms at low incremental effort and cost. FLEX Registry will utilize an adaptive design, where additional targeted substudies and arms can be added after the initial study is opened.

Recruiting

1 award

N/A

3 criteria

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Cema-cel

for B-Cell Lymphoma

This is a randomized, open-label study in adult patients who have completed standard first line therapy for large B-cell lymphoma (LBCL) and achieved a complete response or partial response suitable for observation, but who have minimal residual disease (MRD) as detected by the Foresight CLARITY™ Investigational Use Only (IUO) MRD test, powered by PhasED-Seq™. The purpose of the trial is to assess the efficacy and safety of consolidation with cemacabtagene ansegedleucel (cema-cel), an allogeneic CD19 CAR T product, as compared to standard of care observation. In this study, participants with MRD are randomized 1:1 to treatment with cema-cel or an observation arm. Treatment includes cema-cel following a lymphodepletion regimen of fludarabine and cyclophosphamide. Prior to August 2025, participants may also have received an anti-CD52 monoclonal antibody, ALLO-647, as part of their lymphodepletion regimen.

Recruiting

1 award

Phase 2

5 criteria

More about Jamal Misleh, MD

Clinical Trial Related

3 years of experience running clinical trials · Led 28 trials as a Principal Investigator · 5 Active Clinical Trials

Treatments Jamal Misleh, MD has experience with

  • Pembrolizumab
  • Abemaciclib
  • Placebo
  • LOXO-305
  • Rituximab
  • Botensilimab

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