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NCT00426140 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetics of Patupilone After a Single Intravenous Administration in Patients With Advance Solid Tumor Malignancies.

A Phase 1 study, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
5
Enrollment target

NCT00426140: Completed Phase 1 study, sponsored by Novartis Pharmaceuticals.

NCT00426140 is a Phase 1 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 5 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00426140, a Phase 1 study, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
5 participants
Enrollment target

Study Summary

The main purpose of this study is to characterize the distribution, metabolism, and elimination (ADME) of Patupilone after a single intravenous administration in patients with advanced solid tumor malignancies

Interventions

  • DRUG Patupilone

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2006-08
Phase Phase 1
Novartis Pharmaceuticals

1,375 total trials

What the finished NCT00426140 record still lists

NCT00426140 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower).

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

NCT00426140 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00426140 about?

NCT00426140 is a clinical study titled "Pharmacokinetics of Patupilone After a Single Intravenous Administration in Patients With Advance Solid Tumor Malignancies.". The main purpose of this study is to characterize the distribution, metabolism, and elimination (ADME) of Patupilone after a single intravenous administration in patients with advanced solid tumor malignancies

What is the current status of trial NCT00426140?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 5 participants. The study started on 2006-08.

What interventions are being tested in trial NCT00426140?

The interventions under investigation include: Patupilone (DRUG).

Who is sponsoring clinical trial NCT00426140?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00426140's enrollment target sits among peer trials

5 1989th of 2000 higher than 6 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 NCT00426140, the US trial registry maintained by the National Library of Medicine. NCT00426140 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.