← Eichor
Study identifier: NCT06812858 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

PD-1 Inhibitors Maintenance for cHL Post-autoHCT

Condition: Hodgkin Lymphoma  ·  Sponsor: St. Petersburg State Pavlov Medical University

PhasePhase 2
Planned participants83
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

This phase II study is designed to determine the clinical efficacy of PD-1 inhibitors, administered as maintenance therapy after autologous stem cell transplant (autoHCT), in patients with relapsed or refractory (R/R) classical Hodgkin Lymphoma (cHL)

This description comes directly from the study's public registry record.

Talk to the study team

Polina Kotseliabina, MD  ·  +78123386265  ·  md.FedorovaL@gmail.com

Liudmila Fedorova, MD, PhD  ·  +78123386265  ·  md.FedorovaL@gmail.com

Always discuss trial participation with your own doctor first.

Locations (4)

National Research Oncology CenterAstana, KazakhstanRecruiting
National Medical and Surgical Center named after N.I. PirogovMoscow, RussiaRecruiting
RecruitingP. Hertsen Moscow Oncology Research Institute (MORI) for administrative and economic work - the branch of the FSBI "National Medical Research Radiological Centre" (NMRRC) of the Ministry of Health of the Russian FederationMoscow, RussiaRecruiting
RM Gorbacheva Research Institute, Pavlov UniversitySaint Petersburg, RussiaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06812858