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Terminated Phase 1 Interventional

A Safety Study of SGN-CD19B in Patients With B-cell Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT02702141

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT02702141. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 11, 2026, 10:58 PM EST

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Official title

A Phase 1, Open-label, Dose-escalation Study of SGN-CD19B in Patients With Relapsed or Refractory Aggressive B-cell Non-Hodgkin Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The study will examine the safety profile of SGN-CD19B administered as a single agent. The main purpose of the study is to estimate the highest dose that does not cause unacceptable side effects of SGN-CD19B in patients with relapsed or refractory aggressive B-cell non-Hodgkin lymphoma (NHL) subtypes of diffuse large B-cell lymphoma (DLBCL) and Grade 3 follicular lymphoma (FL3). Additionally, the pharmacokinetic profile and antitumor activity of SGN-CD19B will be assessed.

Study identification

NCT ID
NCT02702141
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Seagen Inc.
Industry
Enrollment
44 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2016 (Actual)
Primary completion
Jul 10, 2018 (Actual)
Completion
Jul 10, 2018 (Actual)
Last update posted
Aug 13, 2018

2016 – 2018

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
14
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
City of Hope National Medical Center Duarte California 91010-3000 —
Mayo Clinic Florida Jacksonville Florida 32224 —
Cardinal Bernardin Cancer Center / Loyola University Medical Center Maywood Illinois 60153 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Mayo Clinic Minnesota Rochester Minnesota 55905 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
New York University (NYU) Cancer Institute New York New York 10016 —
Memorial Sloan Kettering Cancer Center New York New York 10021 —
Cleveland Clinic, The Cleveland Ohio 44195 —
Thomas Jefferson University Philadelphia Pennsylvania 19107 —
Medical University of South Carolina/Hollings Cancer Center Charleston South Carolina 29425 —
University of Utah Salt Lake City Utah 84112 —
Seattle Cancer Care Alliance / University of Washington Seattle Washington 98109-1023 —
Carbone Cancer Center / University of Wisconsin Madison Wisconsin United States —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02702141, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 13, 2018 · Synced Nov 11, 2026

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