Combining pembrolizumab with chemotherapy for relapsed Hodgkin lymphoma
Official title: Phase II Trial of Pembrolizumab in Combination With Salvage Chemotherapy for First-relapsed or Refractory Classical Hodgkin Lymphoma
Run by University of Cologne · NCT04838652 · Data updated 2026-11-12
This study is testing if adding pembrolizumab to standard chemotherapy can help people with relapsed Hodgkin lymphoma feel better and have fewer side effects.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 29 (estimated) |
| Sponsor | University of Cologne Academic / other |
| Drugs / interventions | pembrolizumab, chemotherapy |
| Locations | 1 site (Cologne) |
| Status | Recruiting |
| Started | March 5, 2024 |
| Main results expected | May 2026 |
| Study ends | May 2028 |
| Registry record updated | August 23, 2024 |
| Trial ID | NCT04838652 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals with histologically confirmed first relapse or primary refractory classical Hodgkin lymphoma.
✕Probably not a fit
Patients with nodular lymphocyte-predominant Hodgkin lymphoma or composite lymphoma will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This trial aims to evaluate the effectiveness and safety of pembrolizumab, an anti-PD-1 antibody, in combination with established chemotherapy regimens (ICE or DHAP) for patients with first-relapsed or refractory classical Hodgkin lymphoma. The study seeks to leverage the synergistic effects of checkpoint inhibition alongside conventional chemotherapy to create a more effective treatment option with reduced toxicity. By potentially replacing high-dose chemotherapy, this approach could improve patient outcomes and quality of life.
Why it matters
Potential benefit: If successful, this treatment could provide a more effective and less toxic option for patients with relapsed or refractory classical Hodgkin lymphoma.
How similar studies have gone: Other studies have shown promising results with similar combinations of checkpoint inhibitors and chemotherapy, indicating potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Histologically confirmed first relapse of cHL or primary refractory cHL Exclusion Criteria: * Nodular lymphocyte-predominant Hodgkin lymphoma or composite lymphoma
Where it's running
-
1st Department of Medicine, Cologne University Hospital
Cologne, Germany Recruiting
Study contacts
- Principal investigator: Andreas Engert, Prof. — 1st Department of Medicine, Cologne Universit Hospital
- Study coordinator: Michael Fuchs
- Email: ghsg@uk-koeln.de
- Phone: +49221478
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.