drugset / Trial / NCT04297683

HEALEY ALS Platform Trial - Master Protocol

NCT04297683 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The HEALEY ALS Platform Trial is a perpetual multi-center, multi-regimen clinical trial evaluating the safety and efficacy of investigational products for the treatment of ALS.

Timeline

Start
2020-06-14
Primary completion
2027-07
Completion
2028-08

Outcome

Missed primary endpoint

paper In the primary analysis comparing pridopidine vs the combined placebo groups, there was no significant difference between pridopidine and placebo in the primary end point PMID 40067755 ↗

paper The estimated DRR common to ALSFRS-R and survival was 1.08 (95% credible interval, 0.87-1.31; posterior probability of superiority, 0.24). PMID 39960672 ↗

paper No benefit of CNM-Au8 on ALS disease progression was observed at 24 weeks. PMID 40067821 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject ABBV-CLS-7262 Unknown — Oral
Subject CNM-Au8 Other / unclassified 30 mg Oral
Subject CNM-Au8 Other / unclassified 60 mg Oral
Subject EVETIFATOR Small molecule — Oral
Subject NUZ-001 Unknown — Oral
Subject Pridopidine Small molecule 45 mg Oral
Subject SLS-005 Unknown 0.75 g/kg Other
Subject Verdiperstat Small molecule 600 mg Oral
Subject Zilucoplan Peptide 0.3 mg/kg Subcutaneous