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NCT00058045

A Phase I Study Of Low-Dose Subcutaneous Interleukin 2 (IL-2) And Stem Cell Factor (r-metHuSCF) For Patients With AIDS And AIDS-Associated Malignancy

Completed Phase 1 Last updated 30 January 2013
What this trial tests

Phase 1 trial testing aldesleukin in Lymphoma in 1 participant. Completed.

Timeline
1 August 2002
Primary endpoint
1 November 2003

Quick facts

Lead sponsorRoswell Park Cancer Institute
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Primary purposetreatment
Enrollment1
Start date1 August 2002
Primary completion1 November 2003
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Roswell Park Cancer Institute

Who can join

18 and older, any sex, with Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

RATIONALE: Interleukin-2 may stimulate a person's white blood cells to kill cancer cells. Stem cell factor may increase the number of immune cells found in bone marrow or peripheral blood and may help a person's immune system recover from the side effects of cancer therapy. PURPOSE: Phase I trial to study the effectiveness of combining interleukin-2 with stem cell factor in treating patients who have AIDS or AIDS-related cancer.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of aldesleukin

Trials testing the same drug.

Other recruiting trials for Lymphoma

Currently open trials in the same condition.

Other Roswell Park Cancer Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00058045.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing