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NCT01858922 · ClinicalTrials.gov registry record · Phase 2

Chemotherapy With or Without Radiation, Low and Intermediate Risk Hodgkins Lymphoma, TXCH-HD-12A

A Phase 2 study, sponsored by Baylor College of Medicine.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target

NCT01858922 is a Phase 2 study that has completed, run by Baylor College of Medicine. The registered enrollment target is 40 participants.

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The verdict

NCT01858922, a Phase 2 study, has completed, sponsored by Baylor College of Medicine.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

Subjects have a type of cancer called Hodgkin Disease (HD), a cancer of the lymph system. The lymph system is made up of tissue throughout the body that makes and stores infection-fighting cells. HD is one of the most treatable childhood cancers. The standard treatment for HD involves chemotherapy (treatment with anti-cancer drugs) and radiation therapy (the use of high-dose x-rays to get rid of cancer cells). Although they are cured from their cancer, some patients experience negative side effects from treatment later in life. These kinds of side effects are often referred to as late effects. This can include problems with growth, problems with some organ functions, and sometimes second cancers. These types of effects can be associated with either chemotherapy or radiation therapy. The investigators are therefore designing studies to minimize or prevent these late effects. It is thought that if some patients can be successfully treated without radiation, those patients might experience fewer late side effects. Some patients, however, do not respond as well to the first stages of treatment (slow early responders). Slow early responders are considered to be at higher risk for relapse. This study also looks at whether these kinds of patients will benefit from additional chemotherapy. The purpose of this study is to look at how the immune system recovers and at how certain T-cells in the blood behave after receiving chemotherapy with or without radiation. The investigators also want to identify if bio-markers (special proteins in blood and in cancer) relate to the response of HD to study treatment.

Interventions

  • DRUG ABVE-PC
  • DRUG DECA

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2012-12-19
Est. Completion 2019-08-12
Phase Phase 2

Sponsor

Baylor College of Medicine

616 total trials

What the Registry Record Tells You About NCT01858922

The ClinicalTrials.gov registry entry for NCT01858922 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.

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

NCT01858922 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01858922 about?

NCT01858922 is a clinical study titled "Chemotherapy With or Without Radiation, Low and Intermediate Risk Hodgkins Lymphoma, TXCH-HD-12A". Subjects have a type of cancer called Hodgkin Disease (HD), a cancer of the lymph system. The lymph system is made up of tissue throughout the body that makes and stores infection-fighting cells. HD is one of the most treatable childhood cancers. The standard treatment for HD involves chemotherapy (...

What is the current status of trial NCT01858922?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2012-12-19. Estimated completion is 2019-08-12.

What interventions are being tested in trial NCT01858922?

The interventions under investigation include: ABVE-PC (DRUG), DECA (DRUG).

Who is sponsoring clinical trial NCT01858922?

This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.

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.