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CT1182 Injection, Phase 1, Relapsed Non Hodgkin Lymphoma

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Summary

The NIH has registered a new early Phase 1 clinical trial (NCT07548697) on ClinicalTrials.gov to evaluate the safety, efficacy, metabolic kinetics, and pharmacodynamics of CT1182 injection in patients with relapsed or refractory B-cell non-Hodgkin lymphoma. The single-arm, open-label study targets r/r B-NHL subtypes including DLBCL and Follicular Lymphoma. This is a prospective patient enrollment record; no compliance obligations or regulatory actions are imposed.

“This study is a single arm, open label, dose exploring clinical study to evaluate the safety, efficacy, metabolic kinetics and pharmacodynamics of CT1182 cells in patients with relapsed / refractory B-cell non Hodgkin lymphoma (r/r B-NHL).”

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

The NIH has added a new clinical trial registration (NCT07548697) to ClinicalTrials.gov describing a Phase 1 dose-exploration study of CT1182 injection for relapsed/refractory B-cell non-Hodgkin lymphoma, including DLBCL and Follicular Lymphoma subtypes. The trial will assess safety, efficacy, metabolic kinetics, and pharmacodynamics. This is an informational registry entry with no binding compliance requirements. Clinical investigators, oncology trial sponsors, and hematology/oncology providers should note the trial as a potential enrollment option for eligible patients.

Archived snapshot

Apr 23, 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.

← ClinicalTrials.gov Studies

A Clinical Study Exploring the Safety, Efficacy and Metabolic Kinetics of CT1182 Injection in Patients With Relapsed / Refractory Non Hodgkin Lymphoma

Early Phase 1 NCT07548697 Kind: EARLY_PHASE1 Apr 23, 2026

Abstract

This study is a single arm, open label, dose exploring clinical study to evaluate the safety, efficacy, metabolic kinetics and pharmacodynamics of CT1182 cells in patients with relapsed / refractory B-cell non Hodgkin lymphoma (r/r B-NHL).

Conditions: B-cell Non Hodgkin Lymphoma (NHL), DLBCL - Diffuse Large B Cell Lymphoma, Follicular Lymphoma (FL)

Interventions: CT1182 injection

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Last updated

Classification

Agency
NIH
Published
April 23rd, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Pharmaceutical companies Healthcare providers Clinical investigators
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Clinical trial registration Oncology drug study Pharmacokinetics study
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Clinical Operations
Compliance frameworks
GxP
Topics
Healthcare Public Health

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