Waldenstrom Macroglobulinemia Clinical Trials in Columbus, Ohio
4 studies are recruiting for waldenstrom macroglobulinemia in Columbus, Ohio right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Testing the Combination of Venetoclax and Rituximab, in Comparison to the Usual Treatment (Ibrutinib Plus Rituximab or Zanubrutinib Alone) for Waldenstrom's Macroglobulinemia/Lymphoplasmacytic Lymphoma
This phase II trial studies the effects of venetoclax and rituximab in comparison to ibrutinib and rituximab or zanubrutinib in treating patients with previously untreated Waldenstrom's macroglobulinemia/lymphoplasmacytic lymphoma. Ibrutinib may stop the growth of cancer cells by blocking some of t…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Mount Carmel East Hospital, Columbus, Ohio
- Locations
- 144 in total
- Run by
- National Cancer Institute (NCI)
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A Long-term Extension Study of PCI-32765 (Ibrutinib)
The purpose of this study is to collect long-term safety and efficacy data for participants treated with ibrutinib and to provide ongoing access to ibrutinib for participants who are currently enrolled in ibrutinib studies that have been completed according to the parent protocol, are actively rece…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- The Ohio State University- James Cancer Hospital, Columbus, Ohio
- Locations
- 175 in total
- Run by
- Janssen Research & Development, LLC
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Study of Oral Administration of LP-168 in Patients With Relapsed or Refractory B-cell Malignancies.
This is a phase I, multi-center, open-label, dose-escalation study to evaluate the safety, tolerability, pharmacokinetics and clinical activity of LP-168 in subjects with relapsed or refractory B-cell malignancies. LP-168 is a small molecule inhibitor.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Ohio State University, Columbus, Ohio
- Locations
- 4 in total
- Run by
- Newave Pharmaceutical Inc
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Study of SGR-1505 in Mature B-Cell Neoplasms
The purpose of this study is to evaluate safety and tolerability and to determine the maximum tolerated dose (MTD) or maximum administered dose (MAD) and/or recommended dose (RD) of SGR-1505.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The Ohio State University - The James Cancer Hospital, Columbus, Ohio
- Locations
- 36 in total
- Run by
- Schrödinger, Inc.
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.