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Completed Phase 1Phase 2 Interventional

A Study of ABT-263 in Subjects With Relapsed or Refractory Lymphoid Malignancies

ClinicalTrials.gov ID: NCT00406809

Public ClinicalTrials.gov record NCT00406809. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 7:59 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2a Study Evaluating the Safety, Pharmacokinetics and Efficacy of ABT-263 in Subjects With Relapsed or Refractory Lymphoid Malignancies

Brief summary

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

The Phase 1 portion of the study evaluated the pharmacokinetic profile and safety of ABT-263 with the objective of defining the dose limiting toxicity and maximum tolerated dose in subjects with lymphoid malignancies. The Phase 2a portion of the study is evaluating ABT-263 using a step-up dosing regimen and may be increased to the defined recommended Phase 2 dose to obtain additional safety information and a preliminary assessment of efficacy in subject with lymphoid malignancies. The Extension portion of the study is to allow Phase 2a subjects who remain active 1 year after the last subject enrolls or who have been on study approximately 1 year to continue receiving ABT-263 with less frequent study evaluations. Subjects in the Extension Study will continue receiving study drug for up to 7 years after the last subject transitions to the Extension Study, or until disease progression or toxicity that necessitates discontinuation (whichever comes first).

Study identification

NCT ID
NCT00406809
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
81 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Oct 31, 2006
Primary completion
Sep 30, 2016
Completion
Sep 30, 2016
Last update posted
Aug 1, 2021

2006 – 2016

United States locations

U.S. sites
11
U.S. states
4
U.S. cities
6
Facility City State ZIP Site status
Site Reference ID/Investigator# 4997 Los Angeles California 90033
Site Reference ID/Investigator# 9104 Los Angeles California 90095
Site Reference ID/Investigator# 2613 Bethesda Maryland 20892
Site Reference ID/Investigator# 40243 Boston Massachusetts 02215
Site Reference ID/Investigator# 4745 Boston Massachusetts 02215
Site Reference ID/Investigator# 2628 Buffalo New York 14263
Site Reference ID/Investigator# 23543 New York New York 10016
Site Reference ID/Investigator# 2627 New York New York 10021
Site Reference ID/Investigator# 2614 New York New York 10032
Site Reference ID/Investigator# 5383 New York New York 10065
Site Reference ID/Investigator# 12306 Rochester New York 14642

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00406809, 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 1, 2021 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00406809 live on ClinicalTrials.gov.

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