drugset / Trial / NCT05293171

Study to Investigate the Effect of BL-8040 (Motixafortide) on the QTc Interval in Healthy Subjects

NCT05293171

Phase 1 Completed 38 enrolled BioLineRx, Ltd. Celerion · collab
RandomizedCrossoverTriple-blindOther

Summary

The study will assess the corrected QT (QTc) effects (electrocardiogram \[ECG\]) of motixafortide (BL-8040) 1.25 mg/kg (therapeutic dose) and 2 mg/kg (supratherapeutic dose) following a single subcutaneous (SC) injection relative to placebo in approximately 40 healthy subjects.

Timeline

Start
2021-06-11
Primary completion
2022-06-01
Completion
2022-08-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Motixafortide Peptide 1.25 mg/kg Subcutaneous
Subject Motixafortide Peptide 2 mg/kg Subcutaneous
Comparator Moxifloxacin Small molecule 400 mg Oral

Indications

No indication recorded.