Clin2
NCT05389423Possibly a fitRecruiting

Pomalidomide plus chemotherapy for HIV-related lymphoma

Diffuse Large Cell LymphomaNon-Hodgkin LymphomaBurkitt LymphomaPlasmablastic LymphomaB-Cell Neoplasm

Treatments studied

Part of Blood & lymphatic, Cancer, Immune system & allergy, Infections clinical trials.

This Phase 1 study tests whether a combination of pomalidomide and a dose-adjusted chemotherapy plan (EPOCH), with or without rituximab, can treat certain aggressive B-cell lymphomas in people living with HIV. It aims to find a safe dosing approach and see how well the treatment works for specific lymphoma types or high risk of spread to the brain.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
25 people
Ages
18 years to 120 years
Study type
Interventional

Who can take part

  • You’re age 18 or older and can sign written informed consent.
  • You have confirmed B-cell non-Hodgkin lymphoma, and it includes one of these: fluid/meninges involvement, high risk to relapse in the brain, plasmablastic type, tumor positive for gamma herpesvirus, or presence of Kaposi sarcoma (KS).
  • You have HIV infection (HIV-1 or HIV-2) and are willing to take and stick to HIV treatment (ART).
  • You haven’t had prior “curative-intent” chemotherapy for lymphoma (with limited exceptions if chemo was given briefly before curative treatment).
  • Your scans or tests show lymphoma you can measure or assess, and you meet key blood, liver, and kidney function thresholds.
  • If you can become pregnant, you must take pregnancy tests and use two reliable birth-control methods or commit to abstinence, starting before treatment; if you can father a child, you must use effective contraception and you can’t donate/freeze sperm during the study period.
  • You must be able to safely take aspirin daily (or an approved alternative) and agree to a special pomalidomide risk-management program (REMS).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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