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NCT07066085 · ClinicalTrials.gov registry record · Early Phase 1

Serial Blood Count Study

A Early Phase 1 study of Neutropenia and Congenital Neutropenia, sponsored by University of Washington.

Recruiting
Registry status
Early Phase 1
Development phase
20
Enrollment target
1
Study location

NCT07066085 is a Early Phase 1 study of Neutropenia and Congenital Neutropenia that is actively recruiting participants, run by University of Washington. The registered enrollment target is 20 participants, below the 76-participant average among 12 other Neutropenia trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07066085, a Early Phase 1 study of Neutropenia and Congenital Neutropenia, is actively recruiting participants, sponsored by University of Washington.

RECRUITING
Registry status
Early Phase 1
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

The objective of the Serial Blood Count Study is to determine the utility of home monitoring of white blood cell (WBC) and absolute neutrophil counts (ANC) to diagnose cyclic neutropenia and distinguish between cyclic and severe congenital neutropenia (SCN). A new home monitoring device called Athelas One was granted an FDA 510K Class 2 clearance for evaluation of white blood count (WBC) and absolute neutrophil count (ANC). The investigators believe this device provides a unique and extremely valuable opportunity to for diagnosis of these diseases.

Interventions

  • DEVICE Serial Blood Count Study
  • DEVICE Athelas Home device

Study Locations (1)

Washington

  • University of Washington Medical Center - Montlake - Seattle

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2024-10-17
Est. Completion 2025-12-01
Phase Early Phase 1

Sponsor

University of Washington

1,048 total trials

What the Registry Record Tells You About NCT07066085

The ClinicalTrials.gov registry entry for NCT07066085 describes a study currently listed as recruiting, categorized as Early Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 76-participant average among 12 other Neutropenia trials with a reported enrollment target (74% lower). The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Neutropenia appearing as the primary indexed condition, and to 2 interventions - of which Serial Blood Count Study is the first listed.

NCT07066085 reports 1 study location spanning 1 distinct geographic area - top geographies include Washington.

Frequently Asked Questions

What is clinical trial NCT07066085 about?

NCT07066085 is a clinical study titled "Serial Blood Count Study". The objective of the Serial Blood Count Study is to determine the utility of home monitoring of white blood cell (WBC) and absolute neutrophil counts (ANC) to diagnose cyclic neutropenia and distinguish between cyclic and severe congenital neutropenia (SCN). A new home monitoring device called Athel...

What is the current status of trial NCT07066085?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 20 participants. The study started on 2024-10-17. Estimated completion is 2025-12-01.

What conditions does trial NCT07066085 study?

This clinical trial studies the following conditions: Neutropenia, Congenital Neutropenia, Cyclic Neutropenia.

What interventions are being tested in trial NCT07066085?

The interventions under investigation include: Serial Blood Count Study (DEVICE), Athelas Home device (DEVICE).

Who is sponsoring clinical trial NCT07066085?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07066085 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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