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NCT01938638 · ClinicalTrials.gov registry record · Phase 1

Open Label Phase I Dose Escalation Study With BAY1143572 in Patients With Advanced Cancer

A Phase 1 study, sponsored by Bayer.

Completed
Registry status
Phase 1
Development phase
80
Enrollment target

NCT01938638 is a Phase 1 study that has completed, run by Bayer. The registered enrollment target is 80 participants.

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The verdict

NCT01938638, a Phase 1 study, has completed, sponsored by Bayer.

COMPLETED
Registry status
Phase 1
Development phase
80 participants
Enrollment target

Study Summary

The purpose of this study Part A is to determine the safety, tolerability and the pharmacokinetics of BAY1143572 in subjects with advanced malignancies, which are either refractory to or ineligible for treatment with standard agents. The purpose of this study Part B is: Determine the safety, tolerability, pharmacokinetics (PK) and maximum tolerated dose (MTDG-CSF) of BAY1143572 with concurrent administration of the granulocyte colony-stimulating factors (G-CSF) in an intermittent and continuous dosing schedule in subjects with advanced malignancies.

Interventions

  • DRUG BAY1143572

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2013-09-26
Est. Completion 2016-09-19
Phase Phase 1

Sponsor

Bayer

591 total trials

What the Registry Record Tells You About NCT01938638

The ClinicalTrials.gov registry entry for NCT01938638 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bayer, which has 591 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which BAY1143572 is the first listed.

NCT01938638 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01938638 about?

NCT01938638 is a clinical study titled "Open Label Phase I Dose Escalation Study With BAY1143572 in Patients With Advanced Cancer". The purpose of this study Part A is to determine the safety, tolerability and the pharmacokinetics of BAY1143572 in subjects with advanced malignancies, which are either refractory to or ineligible for treatment with standard agents. The purpose of this study Part B is: Determine the safety, toler...

What is the current status of trial NCT01938638?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2013-09-26. Estimated completion is 2016-09-19.

What interventions are being tested in trial NCT01938638?

The interventions under investigation include: BAY1143572 (DRUG).

Who is sponsoring clinical trial NCT01938638?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.