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Clinical trialNCT07695311Not, yet, recruitingPhase 1Interventional

EWSR1 Immunotherapy in Ewing Sarcoma and DSRCT

SponsorRabi HannaEnrollment24Desmoplastic Small Round Cell TumorEwing Sarcoma
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This study is for people who have high-risk Ewing sarcoma (ES), or a related Ewing's family tumor, desmoplastic small round cell tumor (DSRCT). The purpose of this study is to see if a new EWSR1 immunotherapy (a lipid nanoparticle coated with EWSR1 mRNA) which is given as a shot is safe and whether it can help the body's immune system better recognize and fight cancer. This EWSR1 immunotherapy is designed to target a specific genetic change (EWSR1 fusion gene) that is found in cancer cells but not in normal, healthy cells. Because the EWSR1 gene is broken in cancer cells and the small protein it makes are only in the ES or DSRCT cancer cells, the goal of EWSR1 immunotherapy is to help the immune system identify and attack the cancer without harming normal cells. It is not yet approved by the Food and Drug Administration (FDA). EWSR1 immunotherapy will be given as a shot into the muscle of the arm, leg, or buttock. If participants also receive botensilimab (4 doses after each EWSR1 immunotherapy shot) and balstilimab (an infusion every 2 weeks), these are given intravenously (IV) by a needle in the arm over 30 minutes. Participants in this study will receive treatment for about 6 months or until their cancer gets worse. Participants will remain in the study for follow-up for an additional year, for a total time of about 1.5 years in the study.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Matteo Trucco, MD

    Case Comprehensive Cancer Center, Cleveland Clinic Foundation Taussig Cancer Institute

    Principal Investigator
  • Peter M Anderson, MD, PhD

    Case Comprehensive Cancer Center, Cleveland Clinic Foundation Taussig Cancer Institute

    Principal Investigator
  • Rabi Hanna, MD

    Case Comprehensive Cancer Center, Cleveland Clinic Foundation Taussig Cancer Institute

    Principal Investigator
  • Timothy A Chan, MD, PhD

    Case Comprehensive Cancer Center, Cleveland Clinic Center for Immunotherapy and Immuno-Oncology

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

1 registered facility, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Case Comprehensive Cancer Center, Cleveland Clinic Foundation Taussig Cancer Institute

    Cleveland, Ohio, United States

    Matteo Trucco, MDPeter M Anderson, MD, PhDRabi Hanna, MDTimothy A Chan, MD, PhD

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

BalstilimabBotensilimabEWSR1 immunotherapy
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2026
Primary completion
31 Oct 2029
Completion
31 Jul 2030
Last update posted
16 Jul 2026
Registered enrollment
24
Registry id
NCT07695311

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.