Trial Profile

A 2-Part, Phase 1, Multi-Center, Single-Dose, Open Label, Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of CSL889 in Adult Patients With Sickle Cell Disease

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 19 Sep 2024

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At a glance

Drugs CSL 889 (Primary)
Indications Sickle cell anaemia
Focus Adverse reactions; First in man
Sponsors CSL Behring

Most Recent Events

04 Sep 2023 Status changed from recruiting to completed.
13 Mar 2023 Planned End Date changed from 1 Mar 2023 to 1 Jul 2023.
13 Mar 2023 Planned primary completion date changed from 1 Mar 2023 to 1 Jul 2023.

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