SNV1521 for Advanced Solid Tumors

This study is testing a new oral medication called SNV1521 for people with advanced solid tumors. Researchers want to see if SNV1521 is safe and well-tolerated, and if it can help treat these cancers. They are also exploring different doses and if SNV1521 can be combined with other treatments like DB-1310, Abiraterone, or Darolutamide. You might be able to join if you have an advanced or metastatic (spread to other parts of the body) solid tumor, a good performance status (ECOG 0 or 1), and a life expectancy of over 3 months. The study aims to enroll 400 participants.

Study design
This is an interventional study with a planned enrollment of 400 participants. It is testing different doses of SNV1521, alone or in combination with other drugs.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Safety will be monitored from the first dose through the last dose, up to 13 months. Tolerability will be assessed during the first 28-day cycle.

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

NCT06220864

SNV1521 in Participants With Advanced Solid Tumors

Recruiting
PHASE1Ages 18+InterventionalTreatment
Synnovation Therapeutics, Inc.
~400 participants
Updated 2026-06-25 on ClinicalTrials.gov
What's tested:SNV1521DB-1310AbirateroneDarolutamide

At a glance

Recruiting sites
25 of 25 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety of SNV1521
Measured over From first dose through last dose (up to 13 months)
+1 more outcome measured
Advanced Solid Tumor

NCT06220864

Where you'd take part

This study runs at 25 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • AZ Groeninge

    Kortrijk, Belgiumstudy coordinator listed

    Recruiting

  • AZ Maria Middelares

    Ghent, Belgiumstudy coordinator listed

    Recruiting

  • The Institut Jules Bordet

    Brussels, Belgiumstudy coordinator listed

    Recruiting

  • University Center for Clinical Research Antwerp (UNICCRA)

    Edegem, Belgiumstudy coordinator listed

    Recruiting

  • Arthur J.E. Child Comprehensive Cancer Centre

    Calgary, Alberta, Canadano site contact published

    Recruiting

  • Gustave Roussy

    Villejuif, Franceno site contact published

    Recruiting

  • Institut Bergonie

    Bordeaux, Franceno site contact published

    Recruiting

  • Istituto Clinico Humanitas

    Milan, Italyno site contact published

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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Eligibility criteria

Inclusion

Advanced or metastatic solid tumor malignancy
Evaluable or Measurable disease (RECIST 1.1 Criteria).
ECOG Performance Status 0 or 1.
Life expectancy \> 3 months

Exclusion

History of other malignancy within the past 2 years
Prior diagnosis of Myelodysplastic syndrome or Acute Myeloid Leukemia
Significant cardiovascular disease within 6 months
Significant gastrointestinal disease
HIV infection with a CD4+ T-cell count \< 200 cells/μL and/or a detectable viral load
Liver dysfunction
  • Safety of SNV1521From first dose through last dose (up to 13 months)

    Treatment emergent adverse events (TEAEs)

  • Tolerability of SNV1521DLTs: From first dose through completion of first cycle (28 days)

    Incidence and frequency of dose-limiting toxicities (DLTs) (Dose-escalation arm only)