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NCT01270698 · ClinicalTrials.gov registry record · Phase 1

Study of IMMU-130 in Patients With Relapsed/Refractory Colorectal Cancer

A Phase 1 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 1
Development phase
26
Enrollment target

NCT01270698: Completed Phase 1 study, sponsored by Gilead Sciences.

NCT01270698 is a Phase 1 study that has completed, run by Gilead Sciences. The registered enrollment target is 26 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01270698, a Phase 1 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 1
Development phase
26 participants
Enrollment target

Study Summary

This is a Phase I trial to study the safety of IMMU-130. IMMU-130 is composed of a drug attached to an antibody. The drug is the active ingredient in irinotecan which is a common chemotherapy drug used for colorectal cancer. Antibodies are proteins normally made by the immune system. They bind to substances that don't belong in the body to prevent harm to the body. The antibody in this study was designed to bind to a marker located on colorectal cancer tumors. The antibody was originally made from mouse proteins, but was changed in the laboratory to be more like human antibodies. This study will investigate how IMMU-130 acts for the treatment of colorectal cancer. The study is mainly being done to see if IMMU-130 is safe.

Primary Outcome

The primary outcome measured will be safety of IMMU-130 administered at different dose levels. Safety will be assessed by reviewing the number of adverse events and overall toxicity.

Interventions

  • DRUG IMMU-130

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2011-05
Est. Completion 2014-12
Phase Phase 1
Gilead Sciences

504 total trials

What the finished NCT01270698 record still lists

NCT01270698 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 26 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower).

The record links to 0 conditions, and to 1 intervention - of which IMMU-130 is the first listed.

NCT01270698 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01270698 about?

NCT01270698 is a clinical study titled "Study of IMMU-130 in Patients With Relapsed/Refractory Colorectal Cancer". This is a Phase I trial to study the safety of IMMU-130. IMMU-130 is composed of a drug attached to an antibody. The drug is the active ingredient in irinotecan which is a common chemotherapy drug used for colorectal cancer. Antibodies are proteins normally made by the immune system. They bind to su...

What is the current status of trial NCT01270698?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2011-05. Estimated completion is 2014-12.

What interventions are being tested in trial NCT01270698?

The interventions under investigation include: IMMU-130 (DRUG).

Who is sponsoring clinical trial NCT01270698?

This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01270698's enrollment target sits among peer trials

26 1482nd of 2000 higher than 506 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 NCT01270698, the US trial registry maintained by the National Library of Medicine. NCT01270698 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.