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Spots Global Cancer Trial Database for A Study of Zilovertamab Vedotin (MK-2140) (VLS-101) in Participants With Hematologic Malignancies (MK-2140-001)

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Trial Identification

Brief Title: A Study of Zilovertamab Vedotin (MK-2140) (VLS-101) in Participants With Hematologic Malignancies (MK-2140-001)

Official Title: A Phase 1 Dose-Escalation and Cohort-Expansion Study of VLS-101 in Subjects With Hematological Malignancies (waveLINE-001)

Study ID: NCT03833180

Study Description

Brief Summary: The purpose of this study is to evaluate the safety, pharmacokinetics, immunogenicity, and efficacy of zilovertamab vedotin given intravenously (IV) across a range of dose levels in participants with previously treated hematological cancers including acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), Burkitt lymphoma (BL), chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), lymphoplasmacytoid lymphoma/Waldenström macroglobulinemia (LPL/WM), mantle cell lymphoma (MCL), marginal zone lymphoma (MZL), Richter transformation lymphoma (RTL), and T-cell non-Hodgkin lymphoma (NHL).

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

City of Hope ( Site 0010), Duarte, California, United States

University of California - San Diego ( Site 0003), La Jolla, California, United States

UCLA Hematology & Oncology ( Site 0007), Los Angeles, California, United States

University of Nebraska Medical Center ( Site 0006), Omaha, Nebraska, United States

Northwell Health ( Site 0009), New Hyde Park, New York, United States

Weill Cornell Medical College ( Site 0005), New York, New York, United States

Memorial Sloan Kettering Cancer Center ( Site 0014), New York, New York, United States

University of Rochester ( Site 0008), Rochester, New York, United States

Memorial Sloan-Kettering Cancer Center ( Site 0019), Uniondale, New York, United States

Oregon Health & Science University ( Site 0004), Portland, Oregon, United States

MD Anderson Cancer Center ( Site 0001), Houston, Texas, United States

MD Anderson Cancer Center ( Site 0011), Houston, Texas, United States

University of Virginia Cancer Center ( Site 0012), Charlottesville, Virginia, United States

Swedish Medical Center ( Site 0002), Seattle, Washington, United States

Contact Details

Name: Medical Director

Affiliation: Merck Sharp & Dohme LLC

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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