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Immunosuppressant

Chemotherapy + Stem Cell Transplant for Cancer

Phase 1
Waitlist Available
Research Sponsored by Milton S. Hershey Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
ECOG performance status (PS) 0-2 OR Lansky PS 70-100%
Relapsed or refractory disease
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Study Summary

This trial is giving chemotherapy to young patients with cancer before transplanting stem cells from an umbilical cord in order to stop the growth of tumor cells and help the patient's immune system accept the new stem cells.

Who is the study for?
This trial is for young patients with solid tumors that have come back or didn't respond to treatment. They should not have just a local recurrence over a year after therapy, must have an unrelated cord blood donor, and meet specific health criteria like good heart function and kidney clearance.Check my eligibility
What is being tested?
The study tests if chemotherapy drugs (busulfan, melphalan) and antithymocyte globulin followed by umbilical cord blood transplant can help treat these tumors. It aims to see how well the body tolerates this approach and if it helps fight the cancer.See study design
What are the potential side effects?
Possible side effects include reactions to the immune system suppressants, impact on organ functions from chemotherapy, risk of infection due to immune suppression, and potential graft-versus-host disease where transplanted cells attack the patient's own cells.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I can care for myself and am up and about more than 50% of my waking hours.
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My condition has returned or didn't respond to treatment.
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I have been diagnosed with a solid tumor cancer.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Incidence of graft-versus-host disease
Safety
Secondary outcome measures
Donor/host chimerism status
Immune function post-transplant

Find a Location

Who is running the clinical trial?

Milton S. Hershey Medical CenterLead Sponsor
492 Previous Clinical Trials
2,798,802 Total Patients Enrolled
Kenneth G. Lucas, MDStudy ChairMilton S. Hershey Medical Center
9 Previous Clinical Trials
87 Total Patients Enrolled

Media Library

Antithymocyte Globulin (Immunosuppressant) Clinical Trial Eligibility Overview. Trial Name: NCT00436761 — Phase 1
Solid Tumors Research Study Groups:
Solid Tumors Clinical Trial 2023: Antithymocyte Globulin Highlights & Side Effects. Trial Name: NCT00436761 — Phase 1
Antithymocyte Globulin (Immunosuppressant) 2023 Treatment Timeline for Medical Study. Trial Name: NCT00436761 — Phase 1

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Has this therapy been accepted by the Federal Drug Administration?

"With limited safety and efficacy data, our team has assigned a score of 1 to this treatment. As it is currently in Phase 1 trials, the study's primary focus is on assessing its potential risks and benefits."

Answered by AI

Are there currently any openings for participants in this clinical trial?

"As per clinicaltrials.gov, this research is no longer in need of subjects; the trial was posted on May 1st 2004 and had its last update on December 17th 2013. Nonetheless, there are 2,380 other trials that remain open for recruitment currently."

Answered by AI
~1 spots leftby Apr 2025