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NCT00002571 · ClinicalTrials.gov registry record · Phase 2

SWOG-9320 Combination Chemotherapy, Radiation Therapy, and Antiviral Therapy in Treating Patients With AIDS-Related Lymphoma

A Phase 2 study, sponsored by SWOG Cancer Research Network.

Completed
Registry status
Phase 2
Development phase
52
Enrollment target

NCT00002571: Completed Phase 2 study, sponsored by SWOG Cancer Research Network.

NCT00002571 is a Phase 2 study that has completed, run by SWOG Cancer Research Network. The registered enrollment target is 52 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00002571, a Phase 2 study, has completed, sponsored by SWOG Cancer Research Network.

COMPLETED
Registry status
Phase 2
Development phase
52 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage cancer cells. Antiviral therapy may be effective treatment for AIDS-related lymphoma. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy, radiation therapy, and antiviral therapy in treating patients who have AIDS-related lymphoma.

Interventions

  • DRUG cyclophosphamide
  • BIOLOGICAL filgrastim
  • DRUG doxorubicin hydrochloride
  • DRUG cytarabine
  • BIOLOGICAL bleomycin sulfate

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 1994-06
Est. Completion 2011-07
Phase Phase 2
SWOG Cancer Research Network

270 total trials

What the finished NCT00002571 record still lists

NCT00002571 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 52 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 5 interventions - of which cyclophosphamide is the first listed.

NCT00002571 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00002571 about?

NCT00002571 is a clinical study titled "SWOG-9320 Combination Chemotherapy, Radiation Therapy, and Antiviral Therapy in Treating Patients With AIDS-Related Lymphoma". RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage cancer cells. Antiviral therapy may be effective treatment for AIDS-related lymphoma. PURPOSE: Phase II trial to study the eff...

What is the current status of trial NCT00002571?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 52 participants. The study started on 1994-06. Estimated completion is 2011-07.

What interventions are being tested in trial NCT00002571?

The interventions under investigation include: cyclophosphamide (DRUG), filgrastim (BIOLOGICAL), doxorubicin hydrochloride (DRUG), cytarabine (DRUG), bleomycin sulfate (BIOLOGICAL).

Who is sponsoring clinical trial NCT00002571?

This trial is sponsored by SWOG Cancer Research Network, which has 270 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00002571's enrollment target sits among peer trials

52 1181st of 2000 higher than 811 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT00002571, the US trial registry maintained by the National Library of Medicine. NCT00002571 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.