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NCT03149549 · ClinicalTrials.gov registry record · Phase 1

PROCLAIM-CX-2009: A Trial to Find Safe and Active Doses of an Investigational Drug CX-2009 for Patients With Selected Solid Tumors

A Phase 1 study, sponsored by CytomX Therapeutics.

Terminated
Registry status
Phase 1
Development phase
99
Enrollment target

NCT03149549 is a Phase 1 study that was terminated before completion, run by CytomX Therapeutics. The registered enrollment target is 99 participants.

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The verdict

NCT03149549, a Phase 1 study, was terminated before completion, sponsored by CytomX Therapeutics.

TERMINATED
Registry status
Phase 1
Development phase
99 participants
Enrollment target

Study Summary

The purpose of this first-in-human study of CX-2009 is to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and antitumor activity of CX-2009 in adult subjects with metastatic or locally advanced unresectable solid tumors. PROCLAIM: PRObody CLinical Assessment In Man CX-2009 clinical trial 001 PROBODY is a trademark of CytomX Therapeutics, Inc

Interventions

  • DRUG CX-2009

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2017-06-01
Est. Completion 2020-09-10
Phase Phase 1

Sponsor

CytomX Therapeutics

8 total trials

What the Registry Record Tells You About NCT03149549

The ClinicalTrials.gov registry entry for NCT03149549 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 99 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CytomX Therapeutics, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which CX-2009 is the first listed.

NCT03149549 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03149549 about?

NCT03149549 is a clinical study titled "PROCLAIM-CX-2009: A Trial to Find Safe and Active Doses of an Investigational Drug CX-2009 for Patients With Selected Solid Tumors". The purpose of this first-in-human study of CX-2009 is to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and antitumor activity of CX-2009 in adult subjects with metastatic or locally advanced unresectable solid tumors. PROCLAIM: PRObody CLinical Assessment In Ma...

What is the current status of trial NCT03149549?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 99 participants. The study started on 2017-06-01. Estimated completion is 2020-09-10.

What interventions are being tested in trial NCT03149549?

The interventions under investigation include: CX-2009 (DRUG).

Who is sponsoring clinical trial NCT03149549?

This trial is sponsored by CytomX Therapeutics, which has 8 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.