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Title
Status

 

EMBOLD Sarcoma-202 - Phase 1b/2 Study Evaluating the Efficacy and Safety of Risvutatug Rezetecan in Participants With Previously Treated Unresectable Advanced or Metastatic Sarcomas

Open

EMBOLD Sarcoma-202 - Phase 1b/2 Study Evaluating the Efficacy and Safety of Risvutatug Rezetecan in Participants With Previously Treated Unresectable Advanced or Metastatic Sarcomas

Go to Health Care Provider version

DiagnosisSarcomaStudy StatusOpen
PhaseI/II
Age≥ 12 years of ageRandomisationYES
Line of treatmentDisease relapse or progression
Routes of Treatment AdministrationBiological: Ris-Rez (IV)
Last Posted Update2026-07-24
ClinicalTrials.gov #NCT07602777
International Sponsor
GlaxoSmithKline
Principal Investigators for Canadian Sites
AYA:
McGill University Health Centre - Dr. Saleh
Princess Margaret Cancer Centre (AYA) - Dr. Razak
Centres
Medical contact

Dr. Albiruni Razak

albiruni.razak@uhn.ca

Social worker/patient navigator contact

N/A

Clinical research contact

Jasmine Lee

jasmine.lee@uhn.ca

Medical contact

Sarcoma-Dr. Jonathan Noujaim 

jonathan.noujaim.med@ssss.gouv.qc.ca

Sarcoma-Dr. Ramy Saleh    

 ramy.saleh@mcgill.ca

Social worker/patient navigator contact

N/A

Clinical research contact

Sarcoma - Mahafarin Maralani

mahafarin.maralani@muhc.mcgill.ca

 

 

Study Description

The main goal of this study is to test a new medicine called Risvutatug Rezetecan (Ris-Rez). Researchers want to find out if it can help treat certain types of cancer, if it is safe, how well people tolerate it, and how the body absorbs and breaks down the medicine. This study is for teenagers and adults with osteosarcoma, a type of bone cancer, or soft tissue sarcoma, a type of cancer that starts in soft tissues like muscles, fat, or nerves.

Inclusion Criteria
  • Participants must be 12 years of age or older
  • Participants must have osteosarcoma (bone cancer) or a soft tissue sarcoma that cannot be removed with surgery or has spread to other parts of the body
  • Recent scans must show that the cancer has continued to grow despite the most recent treatment.
  • Participants should be well enough to carry out most daily activities and their overall health should have remained stable during the two weeks before starting the study.
  • Participants must meet organ and lab function requirements 
  • Participants (or a parent/legal guardian) must read, understand, and sign a consent form and agree to follow the study requirements before joining.

Other inclusion and exclusion criteria may apply and will be discussed with you by the study team.