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Active, not recruiting Phase 2 Interventional

Assessing Minimal Residual Disease by Next- Generation Sequencing to Minimize Exposure in People With CLL or SLL Who Have Been Treated With Venetoclax

ClinicalTrials.gov ID: NCT04419519

Public ClinicalTrials.gov record NCT04419519. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 9, 2026, 1:27 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Veneto-STOP Study: Sequential Assessment of Minimal Residual Disease by Next Generation Sequencing to Optimize Outcomes and Minimize Exposure in Venetoclax-Treated CLL/SLL Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will find out whether people with CLL or SLL who have received treatment with venetoclax, either alone or in combination with another drug, and who are found to be MRD-negative, can stop treatment with venetoclax and remain off-treatment for 12 months or more. The researchers will also see whether study participants remain MRD-negative after they stop treatment with venetoclax.

Study identification

NCT ID
NCT04419519
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
81 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 13, 2020 (Actual)
Primary completion
May 2027 (Estimated)
Completion
May 2027 (Estimated)
Last update posted
Jul 10, 2026

2020 – 2027

United States locations

U.S. sites
9
U.S. states
3
U.S. cities
8
Facility City State ZIP Site status
Memorial Sloan Kettering Basking Ridge (All protocol activities) Basking Ridge New Jersey 07920 —
Memorial Sloan Kettering Monmouth (All protocol activities) Middletown New Jersey 07748 —
Memorial Sloan Kettering Bergen (All protocol activities) Montvale New Jersey 07645 —
Memorial Sloan Kettering Commack (All protocol activities) Commack New York 11725 —
Memorial Sloan Kettering Westchester (All protocol activities) Harrison New York 10604 —
Columbia University New York New York 10032 —
Memorial Sloan Kettering Cancer Center (All Protocol Activities) New York New York 10065 —
Memorial Sloan Kettering Nassau (All protocol activities) Uniondale New York 11553 —
University of Washington Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04419519, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 10, 2026 · Synced Nov 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04419519 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →