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NCT00606645 · ClinicalTrials.gov registry record · Phase 1

Safety Study of XmAb®2513 to Treat Hodgkin Lymphoma or Anaplastic Large Cell Lymphoma

A Phase 1 study of Hodgkin Lymphoma and Anaplastic Large Cell Lymphoma, sponsored by Xencor.

Completed
Registry status
Phase 1
Development phase
23
Enrollment target
4
Study locations

NCT00606645 is a Phase 1 study of Hodgkin Lymphoma and Anaplastic Large Cell Lymphoma that has completed, run by Xencor. The registered enrollment target is 23 participants, below the 166-participant average among 71 other Hodgkin Lymphoma trials with a reported enrollment target (86% lower). The trial reports 4 study locations across 4 states.

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The verdict

NCT00606645, a Phase 1 study of Hodgkin Lymphoma and Anaplastic Large Cell Lymphoma, has completed, sponsored by Xencor.

COMPLETED
Registry status
Phase 1
Development phase
23 participants
Enrollment target
4
Study locations

Study Summary

An open-label, multi-dose, single-arm, Phase 1 dose escalation study of XmAb®2513 was conducted to define the MTD or recommended dose(s) for further study, to determine safety and tolerability, to characterize PK and immunogenicity, and to evaluate antitumor activity of XmAb2513 in patients with HL and ALCL (non-cutaneous) and who have received two or more prior therapeutic regimens. There will be no intra-patient dose escalation.

Interventions

  • BIOLOGICAL XmAb2513

Study Locations (4)

Illinois

  • Rush University Medical Center - Chicago

Ohio

  • Ohio State University - Columbus

Pennsylvania

  • Fox Chase Cancer Center - Philadelphia

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2007-12
Est. Completion 2010-04
Phase Phase 1

Sponsor

Xencor

27 total trials

What the Registry Record Tells You About NCT00606645

The ClinicalTrials.gov registry entry for NCT00606645 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 166-participant average among 71 other Hodgkin Lymphoma trials with a reported enrollment target (86% lower). The listed sponsor is Xencor, which has 27 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Hodgkin Lymphoma appearing as the primary indexed condition, and to 1 intervention - of which XmAb2513 is the first listed.

NCT00606645 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Illinois, Ohio, Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00606645 about?

NCT00606645 is a clinical study titled "Safety Study of XmAb®2513 to Treat Hodgkin Lymphoma or Anaplastic Large Cell Lymphoma". An open-label, multi-dose, single-arm, Phase 1 dose escalation study of XmAb®2513 was conducted to define the MTD or recommended dose(s) for further study, to determine safety and tolerability, to characterize PK and immunogenicity, and to evaluate antitumor activity of XmAb2513 in patients with HL ...

What is the current status of trial NCT00606645?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2007-12. Estimated completion is 2010-04.

What conditions does trial NCT00606645 study?

This clinical trial studies the following conditions: Hodgkin Lymphoma, Anaplastic Large Cell Lymphoma.

What interventions are being tested in trial NCT00606645?

The interventions under investigation include: XmAb2513 (BIOLOGICAL).

Who is sponsoring clinical trial NCT00606645?

This trial is sponsored by Xencor, which has 27 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00606645 being conducted?

This trial has 4 study locations across Illinois, Ohio, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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