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Spots Global Cancer Trial Database for PROCLAIM-CX-072: A Trial to Find Safe and Active Doses of an Investigational Drug CX-072 for Patients With Solid Tumors or Lymphomas

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Trial Identification

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

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

Study ID: NCT03013491

Study Description

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:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

PROCLAIM Investigative Site, Los Angeles, California, United States

PROCLAIM Investigative Site, Los Angeles, California, United States

PROCLAIM Investigative Site, New Haven, Connecticut, United States

PROCLAIM Investigative Site, Chicago, Illinois, United States

PROCLAIM Investigative Site, Indianapolis, Indiana, United States

PROCLAIM Investigative Site, Boston, Massachusetts, United States

PROCLAIM Investigative Site, Detroit, Michigan, United States

PROCLAIM Investigative Site, New York, New York, United States

PROCLAIM Investigative Site, New York, New York, United States

PROCLAIM Investigative Site, New York, New York, United States

PROCLAIM Investigative Site, Portland, Oregon, United States

PROCLAIM Investigative Site, Nashville, Tennessee, United States

PROCLAIM Investigative Site, Dallas, Texas, United States

PROCLAIM Investigative Site, Houston, Texas, United States

PROCLAIM Investigative Site, Fairfax, Virginia, United States

PROCLAIM Investigative Site, Madison, Wisconsin, United States

PROCLAIM Investigative Site, Amsterdam, , Netherlands

PROCLAIM Investigative Site, Groningen, , Netherlands

PROCLAIM Investigative Site, Rotterdam, , Netherlands

PROCLAIM Investigative Site, Katowice, , Poland

PROCLAIM Investigative Site, Pamplona, Navarre, Spain

PROCLAIM Investigative Site, Barcelona, , Spain

PROCLAIM Investigative Site, Barcelona, , Spain

PROCLAIM Investigative Site, Madrid, , Spain

PROCLAIM Investigative Site, Madrid, , Spain

PROCLAIM Investigative Ssite, Valencia, , Spain

PROCLAIM Investigative Site, Dnepropetrovsk, , Ukraine

PROCLAIM Invetigative Site, Glasgow, , United Kingdom

PROCLAIM Investigative Site, London, , United Kingdom

PROCLAIM Investigative Site, Manchester, , United Kingdom

PROCLAIM Investigative Site, Newcastle upon Tyne, , United Kingdom

Contact Details

Name: Lawrence Lu, M.D.

Affiliation: CytomX Therapeutics

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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