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Taking people in MexicoPhase 2/3

Tests brentuximab with PD-1 blockade for relapsed Hodgkin lymphoma

Tests brentuximab with PD-1 blockade, then stem cell transplant, in people with returned Hodgkin lymphoma.

Plain-language title generated from the registry record
Registry title: Treatment Strategy for Relapsed/Refractory Hodgkin Lymphoma

Key facts

Where
León, MexicoSee the site
Phase
Phase 2/3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 15 and 90 years old?

Source: NCT05595447, who can take part

Where in Mexico

  • Hospital Regional Alta Especialidad BajioLeón, MexicoTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Hospital Regional de Alta Especialidad del Bajio
Trial code
NCT05595447
Record updated
12 March 2025
Original description
The choice of the best second-line therapy in patients with high LH R/R risk, it is a niche of knowledge not covered at the moment, especially the role of Brentuximab (BV) plus PD-1 blockade and auto-HSCT.Read full original descriptionShow less

Rescue With Brentuximab Plus PD-1 Blockade Followed by Autotransplantation and Consolidation With Brentuximab Plus PD-1 Blockade in Patients With Relapsed/Refractory Hodgkin Lymphoma: Exploratory Single-arm Analysis

The choice of the best second-line therapy in patients with high LH R/R risk, it is a niche of knowledge not covered at the moment, especially the role of Brentuximab (BV) plus PD-1 blockade and auto-HSCT.

What is the progression-free survival and rate of metabolic responses complete in patients with high-risk R/R HL with the treatment strategy: BV+ PD-1 blockade consolidation with Auto-HSCT and maintenance with BV + PD-blockade

1?

Inclusion: Relapsed/refractory Hodgkin lymphoma to ABVD with definition of high risk; Age ≥ 18 years and ≤ 90 years; Adequate liver function, defined as:; Total serum bilirubin ≤ 1.5 x upper limit of normal (ULN); Serum aspartate aminotransferase (AST) ≤ 3.0 x ULN; Serum alanine aminotransferase (ALT) ≤ 3.0 x ULN; Adequate renal functions, defined as:; Serum creatinine ≤ 1.5x ULN or glomerular filtration rate \> 50ml/min; ECOG performance status ≤ 3; Women of reproductive potential should have a serum pregnancy test or negative urine; Prior signature of the informed consent.

Exclusion: Voluntary withdrawal from the study; Develop grade 3 or 4 toxicity according to the INH scale; Loss of follow-up.

ClinicalTrials.gov NCT05595447