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NCT05971251 · ClinicalTrials.gov registry record · Phase 1

Addition of Loncastuximab Tesirine to Acalbrutinib , Chronic Lymphocytic Leukemia

A Phase 1 study of Chronic Lymphocytic Leukemia, sponsored by University of Alabama at Birmingham.

Active
Registry status
Phase 1
Development phase
24
Enrollment target
1
Study location

NCT05971251 is a Phase 1 study of Chronic Lymphocytic Leukemia that is active but no longer recruiting, run by University of Alabama at Birmingham. The registered enrollment target is 24 participants, below the 182-participant average among 187 other Chronic Lymphocytic Leukemia trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05971251, a Phase 1 study of Chronic Lymphocytic Leukemia, is active but no longer recruiting, sponsored by University of Alabama at Birmingham.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

Study is a phase I study to determine the maximum tolerated dose of adding Loncastuximab Tesirine to Aclabrutinib in the treatment of chronic lymphocytic leukemia.

Interventions

  • DRUG Loncastuximab Tesirine and Acalabrutinib

Study Locations (1)

Alabama

  • University of Alabama at Birmingham - Birmingham

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2023-12-18
Est. Completion 2028-12-31
Phase Phase 1

Sponsor

University of Alabama at Birmingham

1,160 total trials

What the Registry Record Tells You About NCT05971251

The ClinicalTrials.gov registry entry for NCT05971251 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 182-participant average among 187 other Chronic Lymphocytic Leukemia trials with a reported enrollment target (87% lower). The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Chronic Lymphocytic Leukemia appearing as the primary indexed condition, and to 1 intervention - of which Loncastuximab Tesirine and Acalabrutinib is the first listed.

NCT05971251 reports 1 study location spanning 1 distinct geographic area - top geographies include Alabama.

Frequently Asked Questions

What is clinical trial NCT05971251 about?

NCT05971251 is a clinical study titled "Addition of Loncastuximab Tesirine to Acalbrutinib , Chronic Lymphocytic Leukemia". Study is a phase I study to determine the maximum tolerated dose of adding Loncastuximab Tesirine to Aclabrutinib in the treatment of chronic lymphocytic leukemia.

What is the current status of trial NCT05971251?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2023-12-18. Estimated completion is 2028-12-31.

What conditions does trial NCT05971251 study?

This clinical trial studies the following conditions: Chronic Lymphocytic Leukemia.

What interventions are being tested in trial NCT05971251?

The interventions under investigation include: Loncastuximab Tesirine and Acalabrutinib (DRUG).

Who is sponsoring clinical trial NCT05971251?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05971251 being conducted?

This trial has 1 study location across Alabama. 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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