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NCT06201507

BV-AVD-R Treatment Children Hodgkin's Lymphoma

Status unknown Phase 2 Last updated 12 January 2024
What this trial tests

Phase 2 trial testing Brentuximab vedotin in Hodgkin Lymphoma in 44 participants. Status unknown.

Timeline
1 October 2022
Primary endpoint
31 December 2024
31 December 2025

Quick facts

Lead sponsorBeijing Children's Hospital
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment44
Start date1 October 2022
Primary completion31 December 2024
Estimated completion31 December 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Beijing Children's Hospital

Who can join

Under 18, any sex, with Hodgkin Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to use modified Brentuximab Vedotin+doxorubicin+vinblastine+dacarbazine+Rituximab(BV-AVD-R) regimen in Chinese Classical Hodgkin's Lymphoma(HL) children. The main questions it aims to answer are: * \[Overall Response Rate(ORR) :Complete Response(CR)+Partial Response(PR)\] * \[progression-free survival (PFS), event-free survival (EFS) and overall survival (OS) at 6 months and 1 year.\] Participants will be given modified BV-AVD-R regimen according to rapid early responders (RER) or slow early responders (SER) after 2 cycles.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Pathobiological Features and Therapeutic Opportunities Linked to TNF Family Member Expression in Classic Hodgkin Lymphoma.
    Alibrahim MN, Gloghini A, Carbone A. · · 2024 · cited 4× · PMID 39682256 · DOI 10.3390/cancers16234070

Verify or expand the search:

Other trials of Brentuximab vedotin

Trials testing the same drug.

Other recruiting trials for Hodgkin Lymphoma

Currently open trials in the same condition.

Other Beijing Children's Hospital trials

Trials by the same sponsor.

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