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This phase III trial compares the effect of continuation of treatment with pembrolizumab (usual approach) to observation only at preventing cancer from coming back in patients with early-stage triple-negative breast cancer (TNBC) who achieved a pathologic complete response after preoperative chemotherapy in combination with pembrolizumab. The usual approach for patients with early-stage TNBC who receive preoperative chemotherapy plus pembrolizumab is to continue to receive pembrolizumab for up to 27 weeks after surgery. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. This trial may help researchers determine if observation is as good as receiving pembrolizumab for 27 weeks after surgery in triple-negative breast cancer patients who achieved a pathologic complete response after preoperative treatment with chemotherapy and pembrolizumab.
CB010A is a study evaluating safety, emerging efficacy, pharmacokinetics and immunogenicity of CB-010 in adults with relapsed/refractory B cell non-Hodgkin lymphoma after lymphodepletion consisting of cyclophosphamide and fludarabine.
This phase III trial compares the effect of adding chemotherapy (doxorubicin or epirubicin hydrochloride [epirubicin] with ifosfamide or dacarbazine) before standard surgery versus surgery alone in improving long-term survival in patients with retroperitoneal sarcomas that are able to be removed by surgery (resectable). Chemotherapy drugs, such as doxorubicin, epirubicin, ifosfamide, and dacarbazine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving chemotherapy before surgery may make the tumor smaller and easier to remove and may increase patient survival, compared to surgery alone.
The purpose of this study is to evaluate the safety and tolerability of AB521 when taken alone in participants with advanced solid tumor malignancies and clear cell renal cell carcinoma (ccRCC).
The goal of this clinical trial is to evaluate the safety of TOS-358 in adults with select solid tumors who meet study enrollment criteria. The main questions it aims to answer are: 1. what is the maximum tolerated dose and recommended dose for phase 2? 2. how safe and tolerable is TOS-358 at different dose levels when taken orally once or twice per day?

Brian Bachmann

Brian Bachmann

brian.bachmann@vanderbilt.edu

Research Program

Have any questions? Contact Us 1-877-936-8422 for more information

Qi Liu, Ph.D., M.S.

  • Professor of Biostatistics
  • Associate Professor of Biomedical Informatics

Qi Liu, Ph.D., M.S.

  • Professor of Biostatistics
  • Associate Professor of Biomedical Informatics

qi.liu@vumc.org

Research Program

Research Description

Have any questions? Contact Us 1-877-936-8422 for more information

Ginger Milne, Ph.D.

  • Research Professor of Medicine
  • Research Professor of Pharmacology

Ginger Milne, Ph.D.

  • Research Professor of Medicine
  • Research Professor of Pharmacology

ginger.milne@vumc.org

Research Program

Research Description

Have any questions? Contact Us 1-877-936-8422 for more information

Robert Carroll, Ph.D., M.S.

  • Associate Professor of Biomedical Informatics

Robert Carroll, Ph.D., M.S.

  • Associate Professor of Biomedical Informatics

robert.carroll@vumc.org

Research Program

Have any questions? Contact Us 1-877-936-8422 for more information

Manus Donahue, Ph.D., M.B.A.

  • Professor of Neurology
  • Professor of Electrical and Computer Engineering
  • Professor of Psychiatry and Behavioral Science

Manus Donahue, Ph.D., M.B.A.

  • Professor of Neurology
  • Professor of Electrical and Computer Engineering
  • Professor of Psychiatry and Behavioral Science

m.donahue@vanderbilt.edu

Research Program

Research Description

Have any questions? Contact Us 1-877-936-8422 for more information
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