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NCT00438802 · ClinicalTrials.gov registry record · Phase 1

Alefacept in Treating Patients With Relapsed or Refractory Cutaneous T-Cell Lymphoma or Peripheral T-Cell Non-Hodgkin's Lymphoma

A Phase 1 study of Lymphoma, sponsored by Mayo Clinic.

Completed
Registry status
Phase 1
Development phase
23
Enrollment target
3
Study locations

NCT00438802: Completed Phase 1 study of Lymphoma, sponsored by Mayo Clinic.

NCT00438802 is a Phase 1 study of Lymphoma that has completed, run by Mayo Clinic. The registered enrollment target is 23 participants, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (95% lower). The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00438802, a Phase 1 study of Lymphoma, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 1
Development phase
23 participants
Enrollment target
3
Study locations

Study Summary

RATIONALE: Combinations of biological substances in alefacept may be able to carry cancer-killing substances directly to cancer cells. PURPOSE: This phase I trial is studying the side effects and best dose of alefacept in treating patients with relapsed or refractory cutaneous T-cell lymphoma or peripheral T-cell non-Hodgkin's lymphoma.

Primary Outcome

The Maximum Tolerated Dose (MTD) will be defined as the highest safely-tolerated dose where at most one out of six patients experiences a Dose Limiting Toxicity (DLT) with the next higher dose level having at least 2 patients who have experienced DLT. The MTD determination will be based on toxicities encountered during the first 8 weeks of treatment.\> \> For this protocol, dose-limiting toxicity (DLT) will be defined as an adverse event attributed (definitely, probably, or possibly) to the stu

Conditions Studied

Interventions

  • DRUG Alefacept

Study Locations (3)

California

  • City of Hope Comprehensive Cancer Center - Duarte

Iowa

  • Holden Comprehensive Cancer Center at University of Iowa - Iowa City

Minnesota

  • Mayo Clinic Cancer Center - Rochester

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2006-03
Est. Completion 2019-07-25
Phase Phase 1
Mayo Clinic

2,844 total trials

What the finished NCT00438802 record still lists

NCT00438802 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (95% lower).

The record links to 1 condition, with Lymphoma appearing as the primary indexed condition, and to 1 intervention - of which Alefacept is the first listed.

NCT00438802 reports a single indexed study location in California, Iowa, Minnesota.

Frequently Asked Questions

What is clinical trial NCT00438802 about?

NCT00438802 is a clinical study titled "Alefacept in Treating Patients With Relapsed or Refractory Cutaneous T-Cell Lymphoma or Peripheral T-Cell Non-Hodgkin's Lymphoma". RATIONALE: Combinations of biological substances in alefacept may be able to carry cancer-killing substances directly to cancer cells. PURPOSE: This phase I trial is studying the side effects and best dose of alefacept in treating patients with relapsed or refractory cutaneous T-cell lymphoma or pe...

What is the current status of trial NCT00438802?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2006-03. Estimated completion is 2019-07-25.

What conditions does trial NCT00438802 study?

This clinical trial studies the following conditions: Lymphoma.

What interventions are being tested in trial NCT00438802?

The interventions under investigation include: Alefacept (DRUG).

Who is sponsoring clinical trial NCT00438802?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00438802 being conducted?

This trial has 3 study locations across California, Iowa, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lymphoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00438802's enrollment target sits among peer trials

23 240th of 299 higher than 58 of 299 other Lymphoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Lymphoma 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 NCT00438802, the US trial registry maintained by the National Library of Medicine. NCT00438802 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.