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NCT00304460 · ClinicalTrials.gov registry record · Phase 1

Mechanism of Action of High-Dose IL-2 (Aldesleukin) in Metastatic Melanoma and Kidney Cancer

A Phase 1 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
138
Enrollment target

NCT00304460: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00304460 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 138 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (130% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00304460, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
138 participants
Enrollment target

Study Summary

Background: -Although IL-2 can shrink tumors in about 20 percent of patients with metastatic kidney cancer and in 15 percent of patients with metastatic melanoma, it is not fully known how the drug works. Objectives: -To better understand how IL-2 causes tumors to shrink. Eligibility: -Patients 18 years of age or older with metastatic kidney cancer or metastatic melanoma Design: * 135 patients with melanoma and 110 patients with kidney cancer may be enrolled. * Patients are hospitalized for about 7 days for each treatment. They receive IL-2 intravenously (through a vein) over 15 minutes every 8 hours for up to 4 days or 12 doses. This constitutes one treatment cycle. * Research blood samples are collected daily during the first treatment cycle and for one or two days following the last dose. * Patients may be asked to undergo leukapheresis, a procedure for collecting large quantities of white blood cells. This involves collecting blood through a needle in an arm vein. The blood is directed through a cell separator where the white cells are extracted. The rest of the blood (red cells, platelets, and plasma) is returned to the patient through the same needle or through a needle in the other arm. * About 7-10 days after discharge from the hospital, patients return for a second treatment cycle but without research blood sampling. * 2 months after therapy, patients are evaluated with scans, and x-rays, and blood tests to evaluate the tumor and the effects of the treatment on immune cells. * Patients whose tumors shrink or remain stable may continue treatment (without repeating the full set of research blood samples) as long as they benefit from the treatment and do not develop unacceptable side effects. Patients who continue treatment are evaluated every 2 months for 3 to 4 times and then every 3 to 6 months.

Interventions

  • BIOLOGICAL aldesleukin

Trial Details

FieldValue
Enrollment Target 138 participants
Start Date 2006-03-13
Est. Completion 2014-02-27
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00304460 record still lists

NCT00304460 is an interventional study that assigns participants to a tested intervention. The registered 138 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (130% higher).

The record links to 0 conditions, and to 1 intervention - of which aldesleukin is the first listed.

NCT00304460 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00304460 about?

NCT00304460 is a clinical study titled "Mechanism of Action of High-Dose IL-2 (Aldesleukin) in Metastatic Melanoma and Kidney Cancer". Background: -Although IL-2 can shrink tumors in about 20 percent of patients with metastatic kidney cancer and in 15 percent of patients with metastatic melanoma, it is not fully known how the drug works. Objectives: -To better understand how IL-2 causes tumors to shrink. Eligibility: -Patients...

What is the current status of trial NCT00304460?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 138 participants. The study started on 2006-03-13. Estimated completion is 2014-02-27.

What interventions are being tested in trial NCT00304460?

The interventions under investigation include: aldesleukin (BIOLOGICAL).

Who is sponsoring clinical trial NCT00304460?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00304460's enrollment target sits among peer trials

138 418th of 2000 higher than 1,581 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

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Source: ClinicalTrials.gov NCT00304460, the US trial registry maintained by the National Library of Medicine. NCT00304460 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.