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Ensayo clínico de fase III para evaluar la seguridad y la eficacia de Efruxifermin en sujetos con esteatohepatitis no alcohólica (EHNA) no cirrótica y fibrosis.

THE PRIMARY OBJECTIVE IN THIS STUDY IS TO EVALUATE THE EFFECT OF EFX COMPARED TO PLACEBO IN ACHIEVING RESOLUTION OF NASH AND REGRESSION OF FIBROSIS IN SUBJECTS WITH STAGE 2 OR 3 FIBROSIS AT WEEK 52

Status
In recruitment
headquarters
Madrid

Technical Summary

  • PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY AND EFFICACY OF EFRUXIFERMIN IN SUBJECTS WITH NON-CIRRHOTIC NON-ALCOHOLIC STEATOHEPATITIS (NASH) AND FIBROSIS
  • Code EudraCT: 2023-505141-48-00
  • Protocol number: AK-US-001-0105
  • Promoter: Akero Therapeutics, Inc
  • Molecule/Drug: Efruxifermin

* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.

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