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NCT05794958 · ClinicalTrials.gov registry record · Phase 1

Evaluate Safety of Axicabtagene Ciloleucel Reinfusion (Axi-Cel-2) in Patients With Relapsed and/or Refractory Second Line High-Risk Non-Hodgkin Lymphoma After Standard of Care Axi-Cel

A Phase 1 study of Non-Hodgkin Lymphoma and Large B-cell Lymphoma, sponsored by Stanford University.

Recruiting
Registry status
Phase 1
Development phase
20
Enrollment target
1
Study location

NCT05794958 is a Phase 1 study of Non-Hodgkin Lymphoma and Large B-cell Lymphoma that is actively recruiting participants, run by Stanford University. The registered enrollment target is 20 participants, below the 151-participant average among 104 other Non-Hodgkin Lymphoma trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05794958, a Phase 1 study of Non-Hodgkin Lymphoma and Large B-cell Lymphoma, is actively recruiting participants, sponsored by Stanford University.

RECRUITING
Registry status
Phase 1
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

This is a phase Ib study to establish safety of Axi-Cel-2 in patients with Large B Cell Lymphoma (LBCL) who are at high risk of relapse.

Interventions

  • DRUG Axicabtagene Ciloleucel

Study Locations (1)

California

  • Stanford University - Palo Alto

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2023-05-23
Est. Completion 2038-04-01
Phase Phase 1

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT05794958

The ClinicalTrials.gov registry entry for NCT05794958 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 151-participant average among 104 other Non-Hodgkin Lymphoma trials with a reported enrollment target (87% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

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

NCT05794958 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT05794958 about?

NCT05794958 is a clinical study titled "Evaluate Safety of Axicabtagene Ciloleucel Reinfusion (Axi-Cel-2) in Patients With Relapsed and/or Refractory Second Line High-Risk Non-Hodgkin Lymphoma After Standard of Care Axi-Cel". This is a phase Ib study to establish safety of Axi-Cel-2 in patients with Large B Cell Lymphoma (LBCL) who are at high risk of relapse.

What is the current status of trial NCT05794958?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2023-05-23. Estimated completion is 2038-04-01.

What conditions does trial NCT05794958 study?

This clinical trial studies the following conditions: Non-Hodgkin Lymphoma, Large B-cell Lymphoma.

What interventions are being tested in trial NCT05794958?

The interventions under investigation include: Axicabtagene Ciloleucel (DRUG).

Who is sponsoring clinical trial NCT05794958?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05794958 being conducted?

This trial has 1 study location across California. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.