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NCT06393465 · ClinicalTrials.gov registry record

Real-World Effectiveness of High-Dose Tafamidis on Neurologic Disease Progression in Mixed-Phenotype Transthyretin Amyloid Cardiomyopathy

A clinical trial of Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM), sponsored by Pfizer.

Active
Registry status
50
Enrollment target
1
Study location

NCT06393465: Active study of Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM), sponsored by Pfizer.

NCT06393465 is a study of Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM) that is active but no longer recruiting, run by Pfizer. The registered enrollment target is 50 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

NCT06393465, a study of Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM), is active but no longer recruiting, sponsored by Pfizer.

ACTIVE NOT RECRUITING
Registry status
50 participants
Enrollment target
1
Study location

Study Summary

This study will examine the clinical effectiveness of Tafamidis in patients with Mixed Phenotype Transthyretin Amyloidosis using data that already exist in patients' medical records

Primary Outcome

Describe and compare the rate of neurologic disease progression before and after initiation of tafamidis in patients with mixed-phenotype ATTR-CM receiving tafamidis 61 mg daily in a real world setting.

Interventions

  • DRUG Tafamidis

Study Locations (1)

New York

  • Pfizer - New York

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2024-06-15
Est. Completion 2026-02-20
Pfizer

1,845 total trials

What the registry record for NCT06393465 still lists

NCT06393465 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target.

The record links to 1 condition, with Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM) appearing as the primary indexed condition, and to 1 intervention - of which Tafamidis is the first listed.

NCT06393465 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT06393465 about?

NCT06393465 is a clinical study titled "Real-World Effectiveness of High-Dose Tafamidis on Neurologic Disease Progression in Mixed-Phenotype Transthyretin Amyloid Cardiomyopathy". This study will examine the clinical effectiveness of Tafamidis in patients with Mixed Phenotype Transthyretin Amyloidosis using data that already exist in patients' medical records

What is the current status of trial NCT06393465?

This trial is currently active not recruiting. The enrollment target is 50 participants. The study started on 2024-06-15. Estimated completion is 2026-02-20.

What conditions does trial NCT06393465 study?

This clinical trial studies the following conditions: Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM).

What interventions are being tested in trial NCT06393465?

The interventions under investigation include: Tafamidis (DRUG).

Who is sponsoring clinical trial NCT06393465?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06393465 being conducted?

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

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Source: ClinicalTrials.gov NCT06393465, the US trial registry maintained by the National Library of Medicine. NCT06393465 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.