Natalie S. Grover - UNC Lineberger

Dr. Natalie S. Grover

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Lineberger Comprehensive Cancer Center at University of North Carolina

Studies Lymphoma
Studies Hodgkin's Lymphoma
10 reported clinical trials
20 drugs studied

Area of expertise

1

Lymphoma

Natalie S. Grover has run 6 trials for Lymphoma. Some of their research focus areas include:

CD30 positive
CD19 positive
Kappa positive
2

Hodgkin's Lymphoma

Natalie S. Grover has run 4 trials for Hodgkin's Lymphoma. Some of their research focus areas include:

Stage IV
Stage III
Stage I

Affiliated Hospitals

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Lineberger Comprehensive Cancer Center At University Of North Carolina

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UNC Lineberger Comprehensive Cancer Center

Clinical Trials Natalie S. Grover is currently running

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Epcoritamab

for Lymphoma

This phase II trial compares epcoritamab to standard practice (observation) for the treatment of patients with B-cell lymphomas who are not in complete remission after treatment with CD19-directed chimeric antigen receptor T-cell (CAR-T) therapy. Epcoritamab is a bispecific antibody. It works by simultaneously attaching to a molecule called CD20 on cancerous B-cells and a molecule called CD3 on effector T-cells, which are a type of immune cell. When epcoritamab binds to CD20 and CD3, it brings the two cells together and activates the T-cells to kill the cancerous B-cells. Epcoritamab may increase a patient's chances of achieving complete remission after CD19-directed CAR-T therapy, compared to standard observation.

Recruiting

1 award

Phase 2

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Cell Therapy

for Hodgkin's Lymphoma

Despite the progress in the therapy, Hodgkin's Lymphoma (HL) remains fatal for more than 15% of patients. Even in patients who are cured, the morbidity of therapy is substantial and long-lasting. New therapeutic agents are required therefore not only to further reduce mortality but also to alleviate morbidity. The majority of HL express the CD30 antigens. CD30 expression is routinely used for the diagnosis of HL. Preclinical observations support CD30 as a viable target of CAR-T therapy. This phase Ib/II study was conducted based on these observations. The purpose of this study is to determine the tolerability of ATLCAR.CD30.CCR4 cells in subjects with Hodgkin's Lymphoma and identify a recommended dose for further. This is a single-center, open-label phase Ib/II trial that uses a 3+3 design to identify a recommended phase 2 dose (RP2D) of ATLCAR.CD30.CCR4 cells in Hodgkin's Lymphoma. The phase II portion is designed to determine the PFS of ATLCAR.CD30.CCR4 in Hodgkin's Lymphoma. Subjects will be enrolled on 1 of 3 dose levels as determined by a 3+3 design. Up to 25 evaluable subjects may then be enrolled in the phase II portion of the study. Subjects may have cells procured to manufacture the ATLCAR.CD30.CCR4 cells if they meet eligibility for procurement. During the time period necessary to manufacture the ATLCAR.CD30.CCR4 cells, Subjects will be allowed to receive standard-of-care bridging therapy at the discretion of their local oncologist. Prior to cell infusion, subjects will undergo additional eligibility evaluations, and then if eligible, will undergo lymphodepletion followed by cell infusion 2-14 days later. Subjects will then be followed for 15 years as is required for studies involving gene transfer experiments.

Recruiting

1 award

Phase 1 & 2

6 criteria

More about Natalie S. Grover

Clinical Trial Related

2 years of experience running clinical trials · Led 10 trials as a Principal Investigator · 5 Active Clinical Trials

Treatments Natalie S. Grover has experience with

  • Nivolumab
  • Bendamustine
  • Cyclophosphamide
  • Fludarabine
  • ATLCAR.CD30.CCR4
  • Brentuximab Vedotin

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