Blood

Autosomal dominant severe congenital neutropenia

0

studies recruiting now

as of 7 Sept 2026

0

studies registered in total

as of 7 Sept 2026

0

countries with a recruiting site

as of 7 Sept 2026

None

recruiting study posted to date

among recruiting studies

Recruiting trials

No registered studies found for Autosomal dominant severe congenital neutropenia.

ClinicalTrials.gov has no study listed under this name as of 7 Sept 2026. That can change, and there are other routes worth knowing about.

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Patient organisations

We do not yet list a dedicated organisation for this condition. The directories below are the best route.

About Autosomal dominant severe congenital neutropenia

RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the genes involved (TCIRG1, ELANE, GFI1, CLPB, SRP19).

Treatments being studied

6 approved treatments and 14 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.

Approved: Eflapegrastim (Rolvedon)Approved: Filgrastim (Accofil)Approved: Posaconazole (Noxafil)Approved: Pegfilgrastim (Cegfila (previously pegfilgrastim mundipharma))Approved: Lipegfilgrastim (Lonquex)Approved: Efbemalenograstim Alfa (Ryzneuta)
Phase 3Mavorixafor (Xolremdi)
Phase 3Alcohol (Ablysinol)
Phase 3Dextrose (Capd)
Phase 3Lithium Carbonate (Camcolit 250)
Phase 3Chlorhexidine
Phase 3Plinabulin
Phase 3Docetaxel (Beizray)
Phase 3Cyclophosphamide (Cyclophosphamide)

+ 6 more in development

Related conditions

Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).