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NCT05293171 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by BioLineRx.

Completed
Registry status
Phase 1
Development phase
38
Enrollment target

NCT05293171: Completed Phase 1 study, sponsored by BioLineRx.

NCT05293171 is a Phase 1 study that has completed, run by BioLineRx. The registered enrollment target is 38 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05293171, a Phase 1 study, has completed, sponsored by BioLineRx.

COMPLETED
Registry status
Phase 1
Development phase
38 participants
Enrollment target

Study 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.

Interventions

  • DRUG 1.25 mg/kg BL-8040 + BL-8040-matching placebo
  • DRUG 2 mg/kg BL-8040
  • DRUG BL-8040-matching placebo
  • DRUG 400 mg Moxifloxacin (1x400 mg tablet)

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2021-06-11
Est. Completion 2022-08-15
Phase Phase 1

Sponsor

BioLineRx

8 total trials

What the Registry Record Tells You About NCT05293171

The ClinicalTrials.gov registry entry for NCT05293171 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BioLineRx, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which 1.25 mg/kg BL-8040 + BL-8040-matching placebo is the first listed.

NCT05293171 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05293171 about?

NCT05293171 is a clinical study titled "Study to Investigate the Effect of BL-8040 (Motixafortide) on the QTc Interval in Healthy Subjects". 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.

What is the current status of trial NCT05293171?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 38 participants. The study started on 2021-06-11. Estimated completion is 2022-08-15.

What interventions are being tested in trial NCT05293171?

The interventions under investigation include: 1.25 mg/kg BL-8040 + BL-8040-matching placebo (DRUG), 2 mg/kg BL-8040 (DRUG), BL-8040-matching placebo (DRUG), 400 mg Moxifloxacin (1x400 mg tablet) (DRUG).

Who is sponsoring clinical trial NCT05293171?

This trial is sponsored by BioLineRx, which has 8 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.