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NCT00051675 · ClinicalTrials.gov registry record · Phase 1

Phase I Study of a Monoclonal Antibody for Treatment of Advanced Adenocarcinomas

A Phase 1 study, sponsored by Xoma (US).

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT00051675: Completed Phase 1 study, sponsored by Xoma (US).

NCT00051675 is a Phase 1 study that has completed, run by Xoma (US). The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00051675, a Phase 1 study, has completed, sponsored by Xoma (US).

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, immunogenicity, and tolerability of a monoclonal antibody administered subcutaneously in the treatment of advanced cancers of the ovary, breast, lung, prostate, colon or rectum that are either refractory to standard therapies or for which therapies that may potentially be of major benefit do not exist.

Interventions

  • DRUG ING-1(heMAb)

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2002-07
Est. Completion 2003-09
Phase Phase 1
Xoma (US)

20 total trials

What the finished NCT00051675 record still lists

NCT00051675 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 1 intervention - of which ING-1(heMAb) is the first listed.

NCT00051675 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00051675 about?

NCT00051675 is a clinical study titled "Phase I Study of a Monoclonal Antibody for Treatment of Advanced Adenocarcinomas". The purpose of this study is to evaluate the safety, immunogenicity, and tolerability of a monoclonal antibody administered subcutaneously in the treatment of advanced cancers of the ovary, breast, lung, prostate, colon or rectum that are either refractory to standard therapies or for which therapie...

What is the current status of trial NCT00051675?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2002-07. Estimated completion is 2003-09.

What interventions are being tested in trial NCT00051675?

The interventions under investigation include: ING-1(heMAb) (DRUG).

Who is sponsoring clinical trial NCT00051675?

This trial is sponsored by Xoma (US), which has 20 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00051675's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 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 NCT00051675, the US trial registry maintained by the National Library of Medicine. NCT00051675 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.