Drugs / HEMOPEXIN (HUMAN)
last change Aug 2025 re-read 3 minutes ago

HEMOPEXIN (HUMAN)

Protein / enzyme biologic

Developed for
sickle cell disease
Investigated by
CSL Behring

Trials 2

2022202320242025202620272028
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT04285827 May 2021 → Jul 2023 sickle cell disease CSL Behring Completed No outcome recorded
Phase 21 trial
Phase 2 NCT06699849 Aug 2025 → Oct 2027 expected sickle cell disease CSL Behring Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2020-11-02 CSL Behring Regulatory Orphan Drug Designation Granted for CSL Behring’s Investigational Plasma-Derived Hemopexin Therapy for Sickle Cell Disease csl.com ↗
CSL Behring announced today that its investigational, plasma-derived hemopexin therapy (CSL889) received orphan drug designation from both the European Commission and the U.S. Food and Drug Administration (FDA) Office of Orphan Products Development for the treatment of sickle cell disease (SCD).

All press releases naming this drug 1 release

DateIssuerRelease

Evidence & citations 7 cited values

Every value below carries the sentence it was read from. 3 sources stand behind the page.

FieldValueCited text
Known as HEMOPEXIN (HUMAN) ChEMBL registry synonym — accepted as the source's own label CHEMBL5315017 ↗
Known as Beta-1b-glycoprotein ChEMBL registry synonym — accepted as the source's own label CHEMBL5315017 ↗
Known as CSL889 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06699849 ↗
1

NCT04285827 ↗

Known as Haemopexin ChEMBL registry synonym — accepted as the source's own label CHEMBL5315017 ↗
Known as Hemopexin (plasma derived) ChEMBL registry synonym — accepted as the source's own label CHEMBL5315017 ↗
Modality Protein / enzyme biologic “CSL889 (human hemopexin)” NCT06699849 ↗
Route Intravenous “Administered as an IV infusion” NCT04285827 ↗