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NCT01139723 · ClinicalTrials.gov registry record · Phase 1

A Study of the Safety and Pharmacokinetics of MINT1526A, Administered Intravenously As a Single Agent and in Combination With Bevacizumab to Patients With Advanced Solid Tumors

A Phase 1 study, sponsored by Genentech.

Completed
Registry status
Phase 1
Development phase
54
Enrollment target

NCT01139723: Completed Phase 1 study, sponsored by Genentech.

NCT01139723 is a Phase 1 study that has completed, run by Genentech. The registered enrollment target is 54 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01139723, a Phase 1 study, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 1
Development phase
54 participants
Enrollment target

Study Summary

This is a Phase I, first-in-human, open label, dose-escalation study of MINT1526A administered alone and in combination with bevacizumab by IV infusion every 3 weeks to patients with advanced solid tumors for whom standard therapy either does not exist or has proven to be ineffective or intolerable.

Interventions

  • DRUG bevacizumab
  • DRUG MINT1526A

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2010-06
Est. Completion 2014-08
Phase Phase 1
Genentech

332 total trials

What the finished NCT01139723 record still lists

NCT01139723 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% lower).

The record links to 0 conditions, and to 2 interventions - of which bevacizumab is the first listed.

NCT01139723 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01139723 about?

NCT01139723 is a clinical study titled "A Study of the Safety and Pharmacokinetics of MINT1526A, Administered Intravenously As a Single Agent and in Combination With Bevacizumab to Patients With Advanced Solid Tumors". This is a Phase I, first-in-human, open label, dose-escalation study of MINT1526A administered alone and in combination with bevacizumab by IV infusion every 3 weeks to patients with advanced solid tumors for whom standard therapy either does not exist or has proven to be ineffective or intolerable.

What is the current status of trial NCT01139723?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2010-06. Estimated completion is 2014-08.

What interventions are being tested in trial NCT01139723?

The interventions under investigation include: bevacizumab (DRUG), MINT1526A (DRUG).

Who is sponsoring clinical trial NCT01139723?

This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01139723's enrollment target sits among peer trials

54 931st of 2000 higher than 1,053 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 NCT01139723, the US trial registry maintained by the National Library of Medicine. NCT01139723 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.