Michael Pulsipher, MD | Aplastic Anemia ...

Dr. Michael Pulsipher, MD

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Children's Hospital Los Angeles

Studies Acute Lymphoblastic Leukemia
Studies Leukemia
16 reported clinical trials
31 drugs studied

Area of expertise

1

Acute Lymphoblastic Leukemia

Michael Pulsipher, MD has run 7 trials for Acute Lymphoblastic Leukemia. Some of their research focus areas include:

CD19 positive
HLA-A positive
HLA-A negative
2

Leukemia

Michael Pulsipher, MD has run 5 trials for Leukemia. Some of their research focus areas include:

CD22 positive
HLA-A positive
HLA-A negative

Affiliated Hospitals

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Children's Hospital Los Angeles

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Children's Hospital Of Los Angeles

Clinical Trials Michael Pulsipher, MD is currently running

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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.

Recruiting

1 award

Phase 2

22 criteria

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NGS Monitoring

for Acute Lymphoblastic Leukemia

Background: Chimeric antigen receptor T-cell (CART) therapy is a form of immunotherapy which can be used to treat people with relapsed B-ALL. For those who achieve remission after CART alone, it may cure up to 50% of people who receive this therapy. However, for people who relapse after CART, it can be hard to achieve remission again. In patients where CART fails, stem cell transplant (HCT) can be used to prevent relapse and achieve cure. But HCT can cause serious side effects. Better testing is needed to distinguish people who can be cured with CART alone from people who may also need to have HCT. Objective: To see if the use of a series of blood and bone marrow tests at regular intervals can help monitor for B-ALL relapse after CART therapy. Eligibility: People aged 1 to 25 years with B-ALL who have had CART therapy within the past 42 days. They must never have had a blood stem cell transplant; they must also have no measurable blood cancer cells. Design: Participants will visit the clinic every 2 weeks starting 42 days after they receive CART therapy. Each visit will be about the same amount of time as a regular clinic visit. about 8 hours. Participants will have blood drawn for testing on each visit. Bone marrow biopsy/aspirate will be done during 4 of the visits at routine timepoints after CART. A needle will be inserted to draw a sample of tissue from inside the bone in the hip. A small amount of blood and tissue will be tested with ClonoSEQ and to evaluate for normal B-cells side by side with the standard tests. The combined testing may help determine whether participants are eligible for HCT and/or at risk of relapse after CART. Participants will be in the study for 2 years.

Recruiting

1 award

N/A

More about Michael Pulsipher, MD

Clinical Trial Related

6 years of experience running clinical trials · Led 16 trials as a Principal Investigator · 5 Active Clinical Trials

Treatments Michael Pulsipher, MD has experience with

  • Fludarabine
  • Cyclophosphamide
  • Tacrolimus
  • Busulfan
  • Methotrexate
  • Tisagenlecleucel

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