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NCT02168140 · ClinicalTrials.gov registry record · Phase 1

CPI-613 and Bendamustine Hydrochloride in Treating Patients With Relapsed or Refractory T-Cell Non-Hodgkin Lymphoma or Hodgkin Lymphoma

A Phase 1 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target

NCT02168140 is a Phase 1 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 16 participants.

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The verdict

NCT02168140, a Phase 1 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

This phase I trial studies the side effects and best dose of CPI-613 when given together with bendamustine hydrochloride in treating patients with relapsed or refractory T-cell non-Hodgkin lymphoma or Hodgkin lymphoma. CPI-613 may kill cancer cells by turning off their mitochondria, which are used by cancer cells to produce energy and are the building blocks needed to make more cancer cells. By shutting off mitochondria, CPI-613 may deprive the cancer cells of energy and other supplies needed to survive and grow. Drugs used in chemotherapy, such as bendamustine hydrochloride, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving CPI-613 with bendamustine hydrochloride may kill more cancer cells.

Interventions

  • DRUG bendamustine hydrochloride
  • DRUG 6,8-bis(benzylthio)octanoic acid

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2014-09
Est. Completion 2022-09-15
Phase Phase 1

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT02168140

The ClinicalTrials.gov registry entry for NCT02168140 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which bendamustine hydrochloride is the first listed.

NCT02168140 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02168140 about?

NCT02168140 is a clinical study titled "CPI-613 and Bendamustine Hydrochloride in Treating Patients With Relapsed or Refractory T-Cell Non-Hodgkin Lymphoma or Hodgkin Lymphoma". This phase I trial studies the side effects and best dose of CPI-613 when given together with bendamustine hydrochloride in treating patients with relapsed or refractory T-cell non-Hodgkin lymphoma or Hodgkin lymphoma. CPI-613 may kill cancer cells by turning off their mitochondria, which are used b...

What is the current status of trial NCT02168140?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2014-09. Estimated completion is 2022-09-15.

What interventions are being tested in trial NCT02168140?

The interventions under investigation include: bendamustine hydrochloride (DRUG), 6,8-bis(benzylthio)octanoic acid (DRUG).

Who is sponsoring clinical trial NCT02168140?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

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

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.