Skip to main navigation Skip to content

Search whole site

Back to all Current clinical trials

Are you living with non-Hodgkin lymphoma that has returned or stopped responding to treatment? Learn about a study of a new treatment option.

The purpose of this study is to assess the safety and potential effectiveness of ARV-393, a new investigational treatment for people with advanced non-Hodgkin lymphoma. The study will help researchers determine the most appropriate dose of ARV-393 and understand how the treatment behaves in the body. Some participants may receive ARV-393 on its own, while others may receive ARV-393 in combination with another anti-cancer treatment called glofitamab. Researchers will also assess whether the treatment can help control or reduce lymphoma.

What you need to know

Who can take part?

Inclusion criteria:
  • Adults aged 18 years and older
  • Diagnosed with non-Hodgkin lymphoma that has returned or stopped responding to treatment
  • Have received at least two previous lines of treatment (some lymphoma subtypes may require at least one prior treatment).

Exclusion criteria
  • Active lymphoma involving the brain or spinal cord
  • Previous stem cell transplant from a donor
  • CAR T-cell therapy within the previous 60 days
  • Active or uncontrolled infection
  • Significant heart disease or poorly controlled high blood pressure
  • Active lung conditions that may increase study risk
  • Pregnant or breastfeeding
  • Another active cancer that may interfere with participation
  • Any medical condition that the study doctor considers may make participation unsuitable
 

What is involved for me?

  • Daily oral ARV-393 treatment in 28-day cycles.
  • Some participants may also receive glofitamab by intravenous (IV) infusion.
  • Follow-up visit approximately 1 month after treatment ends
  • Long-term follow-up every 3 months for up to 2 years
  • Visits occur weekly or every 2 weeks during the first few treatment cycles.
  • CT/PET scans every 8 weeks during the first year, then every 12 weeks.
  • Blood tests, urine tests and vital signs at each visit
  • Regular physical examinations and heart monitoring.

 
Back to all Current clinical trials