Dr. Ryan Lynch, MD

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Fred Hutch/University of Washington Cancer Consortium

Studies Non-Hodgkin's Lymphoma
Studies Hodgkin's Lymphoma
9 reported clinical trials
23 drugs studied

Area of expertise

1Non-Hodgkin's Lymphoma
Ryan Lynch, MD has run 5 trials for Non-Hodgkin's Lymphoma.
2Hodgkin's Lymphoma
Ryan Lynch, MD has run 4 trials for Hodgkin's Lymphoma. Some of their research focus areas include:
Stage I
Stage IV
Stage III

Affiliated Hospitals

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Fred Hutch/University Of Washington Cancer Consortium
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Seattle Cancer Care Alliance / University Of Washington

Clinical Trials Ryan Lynch, MD is currently running

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Polatuzumab Vedotin + Chemotherapy

for Large B-Cell Lymphoma

This phase I trial studies the side effects of polatuzumab vedotin when given with combination chemotherapy with or without glofitamab for the treatment of patients with untreated large B-cell lymphoma that grows and spreads quickly and has severe symptoms (aggressive). Polatuzumab vedotin is a monoclonal antibody, polatuzumab, linked to a toxic agent called vedotin. Polatuzumab attaches to CD79B positive cancer cells in a targeted way and delivers vedotin to kill them. Glofitamab is a monoclonal antibody that may interfere with the ability of cancer cells to grow and spread. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Drugs used in combination chemotherapy such as etoposide, cyclophosphamide, and doxorubicin work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Rituximab is a monoclonal antibody that may interfere with the ability of cancer cells to grow and spread. Anti-inflammatory drugs, such as prednisone, lower the body's immune response and are used with other drugs in the treatment of some types of cancer. Giving polatuzumab vedotin in combination chemotherapy with or without glofitamab may help treat patients with aggressive large B-cell lymphoma.
Recruiting1 award Phase 1
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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.
Recruiting1 award Phase 25 criteria

More about Ryan Lynch, MD

Clinical Trial Related5 years of experience running clinical trials · Led 9 trials as a Principal Investigator · 3 Active Clinical Trials
Treatments Ryan Lynch, MD has experience with
  • Dacarbazine
  • Doxorubicin
  • Rituximab
  • Nivolumab
  • Vinblastine
  • Polatuzumab Vedotin

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