Maintenance Zanzalintinib with Etoposide for Germ Cell Tumor

This study is testing a new combination of two drugs, zanzalintinib and etoposide, for people with germ cell tumors (GCTs) that have come back or are hard to treat. You might be able to join if you have a metastatic GCT that has progressed after initial chemotherapy and at least one other treatment. Researchers want to see how safe this drug combination is and how well it prevents the cancer from growing for 12 months. The study is currently unclear about its recruitment status, but it plans to enroll around 38 participants.

Study design
This is an open-label, single-arm Phase I/II study, meaning all participants will receive the study drugs and everyone will know which drugs are being given. It will initially enroll 9 patients to test different doses of zanzalintinib.
What's involved
You would take zanzalintinib by mouth daily and etoposide by mouth for 21 days of each 28-day cycle. This treatment continues until your cancer progresses or side effects become too severe.
Compensation
Not stated in the trial record.
Follow-up
The study will measure how long you live without your cancer progressing for 12 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06937866

Maintenance Zanzalintinib With Etoposide After HDCT in GCT

Recruiting
PHASE1Ages 18+InterventionalTreatment
Indiana University
~38 participants
Updated 2025-11-21 on ClinicalTrials.gov
What's tested:ZanzalintinibEtoposide Capsule

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Phase 1: Rate of hematologic toxicity
Measured over 28 days
+2 more outcomes measured
Germ Cell Tumor
1 sites across 1 states
Indiana1
  • Jennifer King, MD · PRINCIPAL_INVESTIGATOR · Indiana University Simon Comprehensive Cancer Center

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  • Phase 1: Rate of hematologic toxicity28 days

    Rate of hematologic toxicity including neutropenia, anemia, or thrombocytopenia requiring intervention (transfusions or antibiotics)

  • Phase 1: Rate of non-hematologic toxicity28 days

    Rate of non-hematologic toxicity

  • Phase II: 12-month Progression Free Survival12 months

    12-month PFS based on investigator determination of tumor progression (clinical, radiographic, and/or tumor markers including AFP and hCG)