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NCT02146313 · ClinicalTrials.gov registry record · Phase 1

A Study Evaluating the Safety and Pharmacokinetics of DMUC4064A in Participants With Platinum-Resistant Ovarian Cancer or Unresectable Pancreatic Cancer

A Phase 1 study, sponsored by Genentech.

Completed
Registry status
Phase 1
Development phase
35
Enrollment target

NCT02146313 is a Phase 1 study that has completed, run by Genentech. The registered enrollment target is 35 participants.

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The verdict

NCT02146313, a Phase 1 study, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 1
Development phase
35 participants
Enrollment target

Study Summary

This is a Phase 1, multicenter, open-label, dose-escalation study of DMUC4064A administered by intravenous (IV) infusion every three weeks (q3w) to cancer participants. The study will employ a traditional 3 + 3 dose escalation design to determine the maximum tolerated dose (MTD) of DMUC4064A against platinum-resistant ovarian cancer. Once a q3w recommended Phase 2 dose (RP2D) is identified, two expansion cohorts (one in platinum-resistant ovarian cancer and another in unresectable pancreatic cancer) may be evaluated to further characterize the safety and activity in these populations.

Interventions

  • DRUG DMUC4064A

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2014-06-22
Est. Completion 2018-06-18
Phase Phase 1

Sponsor

Genentech

332 total trials

What the Registry Record Tells You About NCT02146313

The ClinicalTrials.gov registry entry for NCT02146313 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Genentech, which has 332 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which DMUC4064A is the first listed.

NCT02146313 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02146313 about?

NCT02146313 is a clinical study titled "A Study Evaluating the Safety and Pharmacokinetics of DMUC4064A in Participants With Platinum-Resistant Ovarian Cancer or Unresectable Pancreatic Cancer". This is a Phase 1, multicenter, open-label, dose-escalation study of DMUC4064A administered by intravenous (IV) infusion every three weeks (q3w) to cancer participants. The study will employ a traditional 3 + 3 dose escalation design to determine the maximum tolerated dose (MTD) of DMUC4064A against...

What is the current status of trial NCT02146313?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2014-06-22. Estimated completion is 2018-06-18.

What interventions are being tested in trial NCT02146313?

The interventions under investigation include: DMUC4064A (DRUG).

Who is sponsoring clinical trial NCT02146313?

This trial is sponsored by Genentech, which has 332 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.