Viewing Study NCT03013491



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Last Modification Date: 2024-10-26 @ 12:16 PM
Study NCT ID: NCT03013491
Status: COMPLETED
Last Update Posted: 2022-02-09
First Post: 2016-12-26

Brief Title: PROCLAIM-CX-072 A Trial to Find Safe and Active Doses of an Investigational Drug CX-072 for Patients With Solid Tumors or Lymphomas
Sponsor: CytomX Therapeutics
Organization: CytomX Therapeutics

Study Overview

Official Title: An Open-Label Dose-Finding and Proof of Concept Study of the PD-L1 Probody Therapeutic CX-072 as Monotherapy and in Combination With Yervoy Ipilimumab or With Zelboraf Vemurafenib in Subjects With Advanced or Recurrent Solid Tumors or Lymphomas
Status: COMPLETED
Status Verified Date: 2022-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this first-in-human study of CX-072 is to characterize the safety tolerability pharmacokinetics PK pharmacodynamics PD and antitumor activity of CX-072 administered intravenously IV as a single agent or in combination with ipilimumab or vemurafenib in adult subjects with advanced or recurrent solid tumors or lymphomas PROCLAIM-CX-072 PRObody CLinical Assessment In Man CX-072 clinical trial

CX-072 is a Probody therapeutic directed against PD-L1 programmed cell death ligand 1 Probody therapeutics are proteolytically-activatable antibodies Abs designed to widen the therapeutic index by minimizing drug interaction with normal tissue while retaining anti-tumor activity Probody therapeutics are masked to attenuate binding to target in healthy tissue but can become unmasked in the tumor microenvironment by tumor-specific protease activity

PROBODY is a trademark of CytomX Therapeutics Inc
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None