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Clinical Trial

EIM Via the Myolex mScan as an ALS Biomarker

NCT: NCT06491732 · RECRUITING

NCT IDNCT06491732
StatusRECRUITING
Start Date2025-03-01
Completion2027-05-30

Brief Summary

Amyotrophic lateral sclerosis (ALS) has been traditionally considered incurable and untreatable. But starting in the 1990s with the introduction of Riluzole, therapies are being discovered and ultimately approved for slowing disease progression. Many pharmaceutical companies continue to seek new therapeutic approaches. One critical aspect of all clinical trials is the need track to progression sensitively to identify the impact of therapy. Tools to track ALS progression must be convenient, objective, require minimal training, be easily standardized, cost-efficient, and have the potential to be applied effectively at home. There has been a push to identify accurate, objective biomarkers of ALS progression. In this study, the investigators propose to use Electrical impedance myography (EIM) to evaluate the progression of the disease. Work has shown that the EIM 50 kilohertz (kHz) phase value from one or more muscles, followed sequentially, can serve as an effective overall biomarker for assessing the rate of ALS progression for a single person.

Frequently Asked Questions

What is EIM Via the Myolex mScan as an ALS Biomarker?

EIM Via the Myolex mScan as an ALS Biomarker is a clinical trial registered under NCT06491732. Current status: RECRUITING.

What is the status of NCT06491732?

The current status of NCT06491732 (EIM Via the Myolex mScan as an ALS Biomarker) is: RECRUITING.

When did EIM Via the Myolex mScan as an ALS Biomarker start?

EIM Via the Myolex mScan as an ALS Biomarker started on 2025-03-01.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.