Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06484920 · ClinicalTrials.gov registry record · Phase 2

A Phase II Study of the Combination of Pembrolizumab and ATRA Combination Treatment of Relapsed HL and B-NHL

A Phase 2 study of B-cell Lymphoma and Refractory Non-Hodgkin Lymphoma, sponsored by Rita Assi.

Recruiting
Registry status
Phase 2
Development phase
24
Enrollment target
2
Study locations

NCT06484920: Recruiting Phase 2 study of B-cell Lymphoma and Refractory Non-Hodgkin Lymphoma, sponsored by Rita Assi.

NCT06484920 is a Phase 2 study of B-cell Lymphoma and Refractory Non-Hodgkin Lymphoma that is actively recruiting participants, run by Rita Assi. The registered enrollment target is 24 participants, below the 90-participant average among 38 other B-cell Lymphoma trials with a reported enrollment target (73% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06484920, a Phase 2 study of B-cell Lymphoma and Refractory Non-Hodgkin Lymphoma, is actively recruiting participants, sponsored by Rita Assi.

RECRUITING
Registry status
Phase 2
Development phase
24 participants
Enrollment target
2
Study locations

Study Summary

This is a Phase II single-center open label trial of the combination of ATRA and pembrolizumab treatment in patients with histologically proven, relapsed or refractory Hodgkin Lymphoma or B-Non-Hodgkin-lymphoma.

Primary Outcome

Safety will be assess by the NCI Common Terminology Criteria for Adverse Events (CTCAE) v5.0

Interventions

  • DRUG Pembrolizumab
  • DRUG ATRA

Study Locations (2)

Indiana

  • Indiana University Health Melvin and Bren Simon Comprehensive Cancer Center - Indianapolis
  • Sidney and Lois Eskenazi Hospital - Indianapolis

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2024-11-18
Est. Completion 2029-09
Phase Phase 2
Rita Assi

1 total trials

What NCT06484920 shows while recruiting

NCT06484920 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 90-participant average among 38 other B-cell Lymphoma trials with a reported enrollment target (73% lower).

The record links to 5 conditions, with B-cell Lymphoma appearing as the primary indexed condition, and to 2 interventions - of which Pembrolizumab is the first listed.

NCT06484920 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT06484920 about?

NCT06484920 is a clinical study titled "A Phase II Study of the Combination of Pembrolizumab and ATRA Combination Treatment of Relapsed HL and B-NHL". This is a Phase II single-center open label trial of the combination of ATRA and pembrolizumab treatment in patients with histologically proven, relapsed or refractory Hodgkin Lymphoma or B-Non-Hodgkin-lymphoma.

What is the current status of trial NCT06484920?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2024-11-18. Estimated completion is 2029-09.

What conditions does trial NCT06484920 study?

This clinical trial studies the following conditions: B-cell Lymphoma, Refractory Non-Hodgkin Lymphoma, Relapsed Non-Hodgkin Lymphoma, Refractory Hodgkin Lymphoma, Relapsed Hodgkin Lymphoma.

What interventions are being tested in trial NCT06484920?

The interventions under investigation include: Pembrolizumab (DRUG), ATRA (DRUG).

Who is sponsoring clinical trial NCT06484920?

This trial is sponsored by Rita Assi, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06484920 being conducted?

This trial has 2 study locations across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for B-cell Lymphoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06484920's enrollment target sits among peer trials

24 29th of 38 higher than 10 of 38 other B-cell Lymphoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other B-cell Lymphoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06484920, the US trial registry maintained by the National Library of Medicine. NCT06484920 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.