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RecruitingLast updated: 7 April 2026

Evaluating how safe, tolerable and effective the drug Xaluritamig is in people with relapsed or refractory Ewing Sarcoma.A Phase 1b Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of Xaluritamig in Adult, Adolescent and Pediatric Participants With Relapsed or Refractory Ewing Sarcoma

Trial purpose

Medical clipboardCancer treatment

Tumor type

Sarcoma Cancers Sarcoma

Age

People2+

Clinical summary

Summary

The main objectives of this trial are to determine:

  • the recommended dose for expansion for xaluritamig (dose confirmation part only) and
  • the safety and tolerability of xaluritamig in people with relapsed or refractory Ewing Swarcoma.

You may be eligible for this study if you have Ewing Sarcoma (EWS) that is relapsed or refractory following at least 1 line of chemotherapy.

The study has two parts.

Part 1 (Dose Confirmation) will begin with a pre-specified xaluritamig target dose and frequency. Multiple dose levels and/or alternative dose regimens may be explored in parallel to determine 1 or more recommended doses for expansion, which is/are considered safe, based on emerging data.

Participants will be treated in Part 2 (Dose Expansion) after the recommended doses for expansion for xaluritamig are determined in Part 1, to further assess how safe, tolerable and effective the drug is.

Xaluritamig is given via short-term intravenous (IV) infusions.

Conditions

This trial is treating people with relapsed or refractory Ewing Sracoma

Eligibility

Inclusion

  1. Part 1: evaluable disease as defined by RECIST v1.1, as determined by the site investigator.

    Part 2: measurable disease as defined by RECIST v1.1, as determined by the site investigator.

  2. Histologically or cytologically confirmed EWS with molecular evidence of an EWSR1 translocation with an E26 transformation-specific (ETS) family gene, eg, FLI1, ETS-related gene [ERG]) via next generation sequencing (based on local testing).
  3. Relapsed or refractory EWS following at least 1 line of chemotherapy (including treatment with an anthracycline and at least 1 alkylating agent).

  4. Performance status:

    1. Karnofsky ≥ 70% for participants ≥ 16 years of age.
    2. Lansky ≥ 70% for participants < 16 years of age.

  5. Adequate organ function, defined as follows:

    a. Hematological function: i. Absolute neutrophil count ≥ 1.0 x 109/L, provided that:

    • the participant has not received short-acting growth factor support within 7 days before screening assessment, and
    • the participant has not received long-acting growth factor support within 14 days before screening assessment.

    ii. Platelet count ≥ 75 x 109/L, provided that:

    • the participant has not received a platelet transfusion within 7 days before screening assessment, and

    • the participant has not received a platelet stimulating agent within 14 days before screening assessment.

      b. Renal function: i. Estimated glomerular filtration rate based on Modification of Diet in Renal Disease (MDRD) calculation ≥ 30 mL/min/1.73 m^2 for participants ≥ 18 years of age.

    ii. estimated glomerular filtration rate based on Schwartz (2009) calculation ≥ 30 mL/min/1.73 m^2 for participants < 18 years of age.

    c. Hepatic function: i. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 x upper limit of normal (ULN) (or ≤ 5 x ULN for participants with liver metastases).

    ii. Total bilirubin (TBL) ≤ 1.5 x ULN (unless related to Gilbert's or Meulengracht disease).

    d. Pulmonary function: i. Baseline oxygen saturation > 92% in room air at rest and no oxygen supplementation.

    e. Cardiac function: i. Left ventricular ejection fraction ≥ 50%. If left ventricular ejection fraction cannot be measured, then left ventricular fractional shortening ≥ 28%.

  6. Participants of childbearing potential must use protocol-specified contraception to prevent pregnancy during treatment and for an additional 6 months after the last dose of xaluritamig.

Exclusion

  1. Untreated central nervous system (CNS) metastases or leptomeningeal disease. Participants with a history of treated CNS metastases are eligible if there is radiographic evidence of improvement upon the completion of CNS-directed therapy and no evidence of interim progression between the completion of CNS-directed therapy and the screening radiographic study.
  2. History of other malignancy within the past 2 years, except for malignancy treated with curative intent with low risk for recurrence (approximately < 10%) and with no known active disease present for >1 year before enrollment.
  3. Active autoimmune disease that has required systemic treatment (except physiologic adrenal hormone replacement therapy) within the past 2 years or any other diseases requiring immunosuppressive therapy while on study. Participants with Type 1 diabetes, vitiligo, psoriasis, hypo- or hyper-thyroid disease not requiring immunosuppressive treatment are permitted.

  4. Participants who received anti-cancer therapy administered within the following minimum washout periods prior to first dose of xaluritamig:

    1. Cytotoxic chemotherapy: 21 days.
    2. Small molecules including tyrosine kinase inhibitors: 7 days or 5 half-lives, whichever is shorter.
    3. Monoclonal antibodies, immune checkpoint inhibitors, bispecific antibodies and other biologic agents: 28 days or 5 half-lives, whichever is shorter.
    4. Cellular therapies including Chimeric Antigen Receptor T-cell therapy (CAR-T), adoptive T-cell therapy: 56 days.
    5. Radiotherapy: 14 days for focal therapy, 28 days for large field therapy or involving > 30% of the bone marrow.
    6. Stem cell transplant: 12 weeks for autologous, 6 months for allogeneic, with no active graft-versus-host disease.
    7. Any other therapy or investigational agent: 28 days or 5 half-lives, whichever is longer.
  5. Requirement for chronic systemic corticosteroid therapy (prednisone dose > 10 mg/day [> 0.25 mg/kg/day if < 40 kg] or equivalent) or any other immunosuppressive therapies (including anti-tumour necrosis factor α (TNFα) therapies) unless stopped (with adequate tapering) within 28 days before first dose of xaluritamig.
  6. Currently pregnant (confirmed with positive pregnancy test) or breastfeeding or planning to become pregnant, donate eggs, or breastfeed while on trial until an additional 6 months after the last dose of trial intervention.
  7. Unwilling to abstain from donating sperm during treatment and for an additional 6 months after the last dose of xaluritamig.

Inclusion

  • You have had treatment, but your cancer has come back (relapsed or recurrent).
  • You have had treatment but your cancer has gotten worse or has not responded to the treatment you have been given.
  • You have had a certain type of treatment or surgical procedure.

Exclusion

  • You have been diagnosed with a prior or secondary type of cancer.
  • You have certain types of non-cancer medical conditions.
  • You have had certain treatments, surgical procedures or drugs.
Message

Clinical trials have complex eligibility criteria, and other criteria may apply for this trial. Ask your doctor about whether this trial could be right for you.

Participating hospitals

Recruiting hospitals

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Trial Identifiers

Information on this page is partially produced from ClinicalTrials.gov *. View further details about this trial on the registry via the links below:

Trial sponsor

Amgen

Scientific Title

A Phase 1b Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of Xaluritamig in Adult, Adolescent and Pediatric Participants With Relapsed or Refractory Ewing Sarcoma

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