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

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Trial Identification

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

Official Title: A Phase 1-2, Open-Label, Dose-Finding, Proof of Concept, First-in-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CX-2009 in Adults With Metastatic or Locally Advanced Unresectable Solid Tumors (PROCLAIM-CX-2009)

Study ID: NCT03149549

Interventions

CX-2009

Study Description

Brief 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

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

USC Norris Comprehensive Cancer Center, Los Angeles, California, United States

Yale University School of Medicine - Yale Cancer Center, New Haven, Connecticut, United States

Rush University Medical Center, Chicago, Illinois, United States

University of Chicago, Chicago, Illinois, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, United States

New York University (NYU) Clinical Cancer Center, New York, New York, United States

Columbia University College of Physicians & Surgeons, Columbia University, New York, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Providence Portland Medical Center, Portland, Oregon, United States

The Sarah Cannon Research Institute, Nashville, Tennessee, United States

MD Anderson Cancer Center, Houston, Texas, United States

Huntsman Cancer Institute, Salt Lake City, Utah, United States

Viriginia Cancer Specialists, Fairfax, Virginia, United States

Swedish Cancer Institute (SCI), Seattle, Washington, United States

University of Wisconsin-Carbone Cancer Center, Madison, Wisconsin, United States

Amsterdam UMC - Locatie VUmc, Amsterdam, , Netherlands

Universitair Medisch Centrum Groningen, Groningen, , Netherlands

Clinica Universidad de Navarra, Pamplona, Navarre, Spain

Instituto Catalan de Oncologia - Hospital Duran i Reynals, Barcelona, , Spain

Hospital Clinic Barcelona, Barcelona, , Spain

Centro Integral Oncologico Clara Campal, Madrid, , Spain

Instituto Valenciano de Oncologia, Valencia, , Spain

Beatson, West of Scotland Cancer Centre, Glasgow, , United Kingdom

Sarah Cannon Research Institute UK Limited, London, , United Kingdom

Northern Centre for Cancer Care, Newcastle Upon Tyne, , United Kingdom

Contact Details

Name: Monika Vainorius, MD

Affiliation: CytomX Therapeutics

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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