Clinical trial Recruiting at 1 site Phase 2 Interventional Ages 18 to 65

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.

More Classical Hodgkin Lymphoma trials

Quick facts

PhasePhase 2
Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment29 (estimated)
SponsorUniversity of Cologne
Academic / other
Drugs / interventionspembrolizumab, chemotherapy
Locations1 site (Cologne)
StatusRecruiting
StartedMarch 5, 2024
Main results expectedMay 2026
Study endsMay 2028
Registry record updatedAugust 23, 2024
Trial IDNCT04838652 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.