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Clinical Trial

ctDNA-Guided Therapy for Relapsed/Refractory Hodgkin Lymphoma

NCT: NCT07021989 · NOT_YET_RECRUITING

NCT IDNCT07021989
StatusNOT_YET_RECRUITING
Start Date2026-10-01
Completion2034-03-31
SponsorMichael Spinner, MD (OTHER)
First posted
Last updated

Brief Summary

This is a single arm, open-label, multicenter, phase II study of pembrolizumab (pembro), gemcitabine, vinorelbine, and liposomal doxorubicin (GVD) in patients with relapsed or refractory classic Hodgkin lymphoma (cHL) with response-adapted consolidation. This study will investigate using circulating tumor DNA (ctDNA) at pre-determined time points using Foresight CLARITY LDT, an ultra-sensitive liquid biopsy platform that detects Minimal residual disease (MRD) in patients with B-cell lymphomas using the phased variant enrichment and sequencing technology (PhasEDq) to determine response to study interventions.

Frequently Asked Questions

What is ctDNA-Guided Therapy for Relapsed/Refractory Hodgkin Lymphoma?

ctDNA-Guided Therapy for Relapsed/Refractory Hodgkin Lymphoma is a clinical trial registered under NCT07021989. Current status: NOT_YET_RECRUITING.

What is the status of NCT07021989?

The current status of NCT07021989 (ctDNA-Guided Therapy for Relapsed/Refractory Hodgkin Lymphoma) is: NOT_YET_RECRUITING.

When did ctDNA-Guided Therapy for Relapsed/Refractory Hodgkin Lymphoma start?

ctDNA-Guided Therapy for Relapsed/Refractory Hodgkin Lymphoma started on 2026-10-01.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.