Congenital Neutropenia

2

Review clinical trials related to Congenital Neutropenia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

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 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.

Participants needed: 20
Trial details
Phase: Early Phase 1Age: 5+Biological sex: AllType: InterventionalSponsor: University of WashingtonUpdated: Jul 15, 2025Locations: 1
Eligibility criteria

Confirmed diagnosis of severe chronic neutropenia [+6]

Diagnosis of severe chronic neutropenia and negative results for the ELANE mutat... [+4]

Status: Recruiting

Shwachman-Diamond Syndrome Global Patient Survey and Partnering Platform

The Shwachman-Diamond Syndrome Global Patient Survey and Collaboration Program (SDS-GPS) is an opportunity for patients and their families - from anywhere in the world - to share their experience living with SDS via a safe, secure, and convenient online platform, to * expand the understanding of SDS * improve the lives of people with SDS, and * accelerate the development of new therapies and cures for SDS. By joining, participants will receive early access to relevant information about new clinical trials and other research opportunities (such as clinical registries) based on their profile, accelerating research and increasing clinical trial impact and recruitment success. The platform, consent forms, and surveys are available in five languages: English, Spanish, French, German, and Italian. More languages to come.

Participants needed: 8,000
Trial details
Biological sex: AllType: ObservationalSponsor: Shwachman-Diamond Syndrome Alliance IncUpdated: May 31, 2025Locations: 1Duration: 120 Years
Eligibility criteria

Patients with a confirmed Shwachman-Diamond Syndrome (SDS) diagnosis, including... [+3]