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Study on the Treatment of Double/Triple-hit DLBCL With Chidamide and Lisaftoclax in Combination With Pola-R-CHP

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Summary

Phase 2 clinical trial NCT07552324 registered April 27, 2026, evaluating CL-Pola-R-CHP regimen in patients aged 65 and older with double/triple-hit diffuse large B-cell lymphoma (DHL/THL) who are not suitable for transplantation. The open-label multicenter study employs a 6-cycle treatment with 21-day intervals. This is a study registration entry on ClinicalTrials.gov and does not impose compliance obligations on regulated entities.

“This is an open-label, multicenter clinical study for patients aged 65 and above with double/triple-hit diffuse large B-cell lymphoma who are not suitable for transplantation.”

NIH , verbatim from source
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About this source

ClinicalTrials.gov is the NIH-run registry of every clinical trial conducted in the United States, plus most international trials sponsored by US-based companies or institutions. By federal law, sponsors must register Phase 2 through Phase 4 studies before enrolling patients and post results within a year of completion. This feed tracks every new trial registration and study update, around 700 a month: drug interventions, device studies, behavioral protocols, observational research. Watch this if you scout drug candidates moving into mid or late-stage development, monitor competitor pipelines, or follow rare disease research where new trials signal patient hope. GovPing parses sponsor, phase, intervention, and target indication on each entry.

What changed

Phase 2 clinical trial NCT07552324 was registered on ClinicalTrials.gov on April 27, 2026, documenting a study of the CL-Pola-R-CHP regimen for double/triple-hit diffuse large B-cell lymphoma (DHL/THL) in patients aged 65 and above who are ineligible for transplantation. The study employs an open-label, multicenter design with 6 treatment cycles repeated every 21 days.

Healthcare providers and clinical investigators should note this as an active Phase 2 enrollment opportunity for elderly lymphoma patients. Pharmaceutical companies developing related agents may track this as competitive landscape information. The registration is informational and does not create regulatory compliance obligations.

Archived snapshot

Apr 27, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Study on the Treatment of Double/Triple-hit DLBCL With Chidamide and Lisaftoclax in Combination With Pola-R-CHP

Phase 2 NCT07552324 Kind: PHASE2 Apr 27, 2026

Abstract

This is an open-label, multicenter clinical study for patients aged 65 and above with double/triple-hit diffuse large B-cell lymphoma who are not suitable for transplantation. The study employs a 6-cycle CL-Pola-R-CHP regimen, with cycles repeated every 21 days.

Conditions: DHL, THL, DLBCL - Diffuse Large B Cell Lymphoma

Interventions: CL-Pola-R-CHP

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Last updated

Classification

Agency
NIH
Published
April 27th, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Healthcare providers Pharmaceutical companies
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Clinical trial registration Drug development Oncology treatment
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Regulatory Affairs
Topics
Healthcare Medical Devices

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