Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01477021 · ClinicalTrials.gov registry record · Phase 1

Autologous T Cells and Cyclophosphamide in Treating Patients With Soft Tissue Sarcoma That is Metastatic or Cannot Be Removed By Surgery

A Phase 1 study, sponsored by Fred Hutchinson Cancer Center.

Completed
Registry status
Phase 1
Development phase
6
Enrollment target

NCT01477021: Completed Phase 1 study, sponsored by Fred Hutchinson Cancer Center.

NCT01477021 is a Phase 1 study that has completed, run by Fred Hutchinson Cancer Center. The registered enrollment target is 6 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01477021, a Phase 1 study, has completed, sponsored by Fred Hutchinson Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

This phase I trial studies the side effects and how well giving autologous T cells with cyclophosphamide works in treating patients with soft tissue sarcoma that is metastatic or cannot be removed by surgery. Biological therapies, such as cellular adoptive immunotherapy, may stimulate the immune system in different ways and stop cancer cells from growing. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving autologous T cells together with cyclophosphamide may kill more tumor cells.

Primary Outcome

Patients will be monitored for treatment-related toxicities. All unexpected grade 3, 4, and 5 toxicities will be reported descriptively.

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG cyclophosphamide
  • BIOLOGICAL NY-ESO-1-specific T cells

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2012-01
Phase Phase 1
Fred Hutchinson Cancer Center

483 total trials

What the finished NCT01477021 record still lists

NCT01477021 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 3 interventions - of which laboratory biomarker analysis is the first listed.

NCT01477021 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01477021 about?

NCT01477021 is a clinical study titled "Autologous T Cells and Cyclophosphamide in Treating Patients With Soft Tissue Sarcoma That is Metastatic or Cannot Be Removed By Surgery". This phase I trial studies the side effects and how well giving autologous T cells with cyclophosphamide works in treating patients with soft tissue sarcoma that is metastatic or cannot be removed by surgery. Biological therapies, such as cellular adoptive immunotherapy, may stimulate the immune sys...

What is the current status of trial NCT01477021?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2012-01.

What interventions are being tested in trial NCT01477021?

The interventions under investigation include: laboratory biomarker analysis (OTHER), cyclophosphamide (DRUG), NY-ESO-1-specific T cells (BIOLOGICAL).

Who is sponsoring clinical trial NCT01477021?

This trial is sponsored by Fred Hutchinson Cancer Center, which has 483 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01477021's enrollment target sits among peer trials

6 1974th of 2000 higher than 12 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01477021, the US trial registry maintained by the National Library of Medicine. NCT01477021 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.