Rare condition

Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation

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 Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation.

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 Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation

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 gene involved (SERPINA1).

Treatments being studied

10 approved treatments and 7 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.

Approved: Idecabtagene Vicleucel (Abecma)Approved: Protamine Sulfate (Prosulf)Approved: ThrombinApproved: Phytonadione (Aquamephyton)Approved: Coagulation Factor Ix Recombinant Human (Benefix)Approved: Aprotinin (Trasylol)Approved: Pentastarch (Infukoll)Approved: Aminocaproic Acid (Amicar)Approved: Ethanolamine Oleate (Ethamolin)Approved: Dicumarol (Dicumarol)
Phase 3Vatreptacog Alfa (Activated)
Phase 3Eptacog Alfa (Activated) (Novoseven)
Phase 2/3Heparin
Phase 2/3Argatroban (Acova)
Phase 2Catridecacog (Novothirteen)
Phase 1Von Willebrand Factor Human (Von willebrand factor human component of voncento)
PREAPPROVALAndexanet Alfa (Ondexxya)

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).