Phase 2Active, not recruitingAge-related condition

Study of Re-Treatment With ALXN2220 in Patients With ATTR-CM

A Phase 2, Single Arm, Multicenter Study to Evaluate the Pharmacodynamics and Safety of Re-Treatment With ALXN2220 in Patients With Transthyretin Amyloid Cardiomyopathy

Sponsor
Neurimmune AG (Industry)
Enrolment
35 planned
Conditions
Amyloid Transthyretin Cardiomyopathy
Interventions
ALXN2220
Ages
adults, older adults
Registry
NCT07213583, CTIS2025-520506-35-00

Full record on ClinicalTrials.gov

From the registry

This is a Phase 2, single-arm, multicenter study to evaluate the pharmacodynamics and safety of re-treatment with ALXN2220 in previous participants of Study NI006-101.

Primary outcomes

  • Change from Baseline to Week 48 in ECV measured by cMRI
  • Change from Baseline to Week 48 in Heart Retention/Whole Body Retention measured by scintigraphy

History

  1. Primary completion expected

  2. Last registry update

  3. Registered

  4. Started