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NCT07151820 · ClinicalTrials.gov registry record

A Real-world Study About the Impact of Adverse Events (AEs) on Treatment Adjustments, Healthcare Resource Use, and Costs Among Chronic Myeloid Leukemia Patients

A clinical trial of Leukemia, Chronic Myeloid, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
2,546
Enrollment target
1
Study location

NCT07151820: Completed study of Leukemia, Chronic Myeloid, sponsored by Novartis Pharmaceuticals.

NCT07151820 is a study of Leukemia, Chronic Myeloid that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 2,546 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07151820, a study of Leukemia, Chronic Myeloid, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
2,546 participants
Enrollment target
1
Study location

Study Summary

The aim of this study was to assess the frequency of adverse events (AEs) experienced by chronic myeloid leukemia (CML) patients treated with tyrosine kinase inhibitors (TKIs) and evaluate their impact on treatment adjustments as well as the burden of AEs on healthcare resource use (HRU) and costs. This study used real-world administrative claims data from the PharMetrics Plus database. AEs of interest were selected based on information obtained from the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines, Chronic Myeloid Leukemia Version 1. 2024 and clinical inputs. Given the nature of claims data, only AEs of interest that required medical attention (i.e., resulted in a claim record) were captured in this study.

Primary Outcome

The Study Period spanned from treatment initiation until treatment discontinuation, one day before treatment switch to another CML treatment, end of data availability, end of health plan coverage, or death, whichever came first.

Conditions Studied

Study Locations (1)

New Jersey

  • Novartis - East Hanover

Trial Details

FieldValue
Enrollment Target 2,546 participants
Start Date 2024-04-08
Est. Completion 2024-10-22
Novartis Pharmaceuticals

1,375 total trials

What the finished NCT07151820 record still lists

NCT07151820 is an observational study that tracks outcomes without assigning an intervention. Its 2,546 participants enrollment target places it among the larger protocols in the corpus.

The record links to 1 condition, with Leukemia, Chronic Myeloid appearing as the primary indexed condition, and to 0 interventions.

NCT07151820 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT07151820 about?

NCT07151820 is a clinical study titled "A Real-world Study About the Impact of Adverse Events (AEs) on Treatment Adjustments, Healthcare Resource Use, and Costs Among Chronic Myeloid Leukemia Patients". The aim of this study was to assess the frequency of adverse events (AEs) experienced by chronic myeloid leukemia (CML) patients treated with tyrosine kinase inhibitors (TKIs) and evaluate their impact on treatment adjustments as well as the burden of AEs on healthcare resource use (HRU) and costs. ...

What is the current status of trial NCT07151820?

This trial is currently completed. The enrollment target is 2,546 participants. The study started on 2024-04-08. Estimated completion is 2024-10-22.

What conditions does trial NCT07151820 study?

This clinical trial studies the following conditions: Leukemia, Chronic Myeloid.

Who is sponsoring clinical trial NCT07151820?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07151820 being conducted?

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

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Source: ClinicalTrials.gov NCT07151820, the US trial registry maintained by the National Library of Medicine. NCT07151820 (large enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.