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NCT05053659 · ClinicalTrials.gov registry record · Phase 1

Loncastuximab Tesirine and Venetoclax for Relapsed/ Refractory Non-Hodgkin Lymphoma

A Phase 1 study of Refractory Non-Hodgkin Lymphoma and Relapsed Non-Hodgkin Lymphoma, sponsored by Paolo Caimi, MD.

Active
Registry status
Phase 1
Development phase
23
Enrollment target
1
Study location

NCT05053659: Active Phase 1 study of Refractory Non-Hodgkin Lymphoma and Relapsed Non-Hodgkin Lymphoma, sponsored by Paolo Caimi, MD.

NCT05053659 is a Phase 1 study of Refractory Non-Hodgkin Lymphoma and Relapsed Non-Hodgkin Lymphoma that is active but no longer recruiting, run by Paolo Caimi, MD. The registered enrollment target is 23 participants, below the 95-participant average among 17 other Refractory Non-Hodgkin Lymphoma trials with a reported enrollment target (76% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05053659, a Phase 1 study of Refractory Non-Hodgkin Lymphoma and Relapsed Non-Hodgkin Lymphoma, is active but no longer recruiting, sponsored by Paolo Caimi, MD.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
23 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine the correct dose and safety of combining two new cancer drugs, loncastuximab tesirine and venetoclax, as a treatment for relapsed or refractory B cell lymphoma.These drugs are used to treat some lymphomas, but have not yet been tested in combination for the treatment of lymphoma. The main goal of this study is to determine the safety of the combination.

Primary Outcome

Number of DLTs during cycle 1 (21 days) of loncastuximab tesirine and venetoclax

Interventions

  • DRUG Venetoclax
  • DRUG Loncastuximab tesirine

Study Locations (1)

Ohio

  • Cleveland Clinic Taussig Cancer Center, Case Comprehensive Cancer Center - Cleveland

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2022-06-20
Est. Completion 2026-06
Phase Phase 1
Paolo Caimi, MD

5 total trials

What the registry record for NCT05053659 still lists

NCT05053659 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 95-participant average among 17 other Refractory Non-Hodgkin Lymphoma trials with a reported enrollment target (76% lower).

The record links to 2 conditions, with Refractory Non-Hodgkin Lymphoma appearing as the primary indexed condition, and to 2 interventions - of which Venetoclax is the first listed.

NCT05053659 reports a single indexed study location in Ohio.

Frequently Asked Questions

What is clinical trial NCT05053659 about?

NCT05053659 is a clinical study titled "Loncastuximab Tesirine and Venetoclax for Relapsed/ Refractory Non-Hodgkin Lymphoma". The purpose of this study is to determine the correct dose and safety of combining two new cancer drugs, loncastuximab tesirine and venetoclax, as a treatment for relapsed or refractory B cell lymphoma.These drugs are used to treat some lymphomas, but have not yet been tested in combination for the ...

What is the current status of trial NCT05053659?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2022-06-20. Estimated completion is 2026-06.

What conditions does trial NCT05053659 study?

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

What interventions are being tested in trial NCT05053659?

The interventions under investigation include: Venetoclax (DRUG), Loncastuximab tesirine (DRUG).

Who is sponsoring clinical trial NCT05053659?

This trial is sponsored by Paolo Caimi, MD, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05053659 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Refractory Non-Hodgkin 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 NCT05053659's enrollment target sits among peer trials

23 14th of 17 higher than 4 of 17 other Refractory Non-Hodgkin Lymphoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Refractory Non-Hodgkin 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

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Source: ClinicalTrials.gov NCT05053659, the US trial registry maintained by the National Library of Medicine. NCT05053659 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.