Dr. David Russler-Germain, M.D., Ph.D.

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Washington University School of Medicine

Studies Lymphoma
Studies Follicular Lymphoma
4 reported clinical trials
7 drugs studied

Area of expertise

1

Lymphoma

David Russler-Germain, M.D., Ph.D. has run 3 trials for Lymphoma. Some of their research focus areas include:

Stage III
Stage IV
Stage II
2

Follicular Lymphoma

David Russler-Germain, M.D., Ph.D. has run 3 trials for Follicular Lymphoma. Some of their research focus areas include:

Stage III
Stage IV
Stage II

Affiliated Hospitals

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Washington University School Of Medicine

Clinical Trials David Russler-Germain, M.D., Ph.D. is currently running

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Mosunetuzumab

for Aggressive B-Cell Lymphoma

This phase 1 pilot study examines the feasibility and safety of mosunetuzumab after autologous stem cell transplant for patients with aggressive B cell lymphomas. Mosunetuzumab is an antibody that has been engineered to attach to two target cells in the immune system: T cells that normally perform tasks like killing virus-infected cells, and cancerous B cells. Mosunetuzumab has been designed to direct these T cells to kill the cancerous B cells instead.

Recruiting

2 awards

Phase 1

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Thiotepa + Stem Cell Transplant

for Lymphoma

A serious consequence of systemic diffuse large B-cell lymphoma (DLBCL) is secondary central nervous system (CNS) relapse, which occurs in approximately 5% of all patients. Many CNS relapses occur within the first year after completion of frontline treatment and are associated with significantly increased mortality; thus, it is important to tailor frontline treatment to provide prophylaxis against CNS relapse in those patients who are determined to be high-risk. Autologous stem cell transplantation (ASCT) is standard of care for patients with DLBCL who relapse one year or more after first remission, and it has been shown to improve progression-free survival for patients with primary CNS lymphoma. The four-drug BEAM regimen (carmustine, etoposide, cytarabine, and melphalan) is the preferred conditioning regimen for DLBCL patients undergoing ASCT; however, patients with primary CNS lymphoma receive thiotepa plus carmustine as their conditioning regimen due to its better CNS penetration. This study tests the hypothesis that consolidation thiotepa/carmustine ASCT in first complete remission will reduce the risk of CNS relapse in transplant-eligible patients with DLBCL with no prior CNS disease at high risk of secondary CNS recurrence.

Recruiting

1 award

Phase 2

3 criteria

More about David Russler-Germain, M.D., Ph.D.

Clinical Trial Related

3 years of experience running clinical trials · Led 4 trials as a Principal Investigator · 2 Active Clinical Trials

Treatments David Russler-Germain, M.D., Ph.D. has experience with

  • Mosunetuzumab
  • Polatuzumab Vedotin
  • DHAX
  • ICE
  • Autologous Stem Cell Transplant
  • Carmustine

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