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Spots Global Cancer Trial Database for Study of ALXN1830 Administered Subcutaneously in Adults With Generalized Myasthenia Gravis

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Trial Identification

Brief Title: Study of ALXN1830 Administered Subcutaneously in Adults With Generalized Myasthenia Gravis

Official Title: A Phase 2a Randomized, Double-blind, Placebo-controlled, Parallel Groups, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ALXN1830 Administered Subcutaneously in Adult Patients With Generalized Myasthenia Gravis

Study ID: NCT04982289

Interventions

ALXN1830
Placebo

Study Description

Brief Summary: This study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics (PD), immunogenicity, and efficacy of subcutaneous (SC) ALXN1830 in adults with generalized myasthenia gravis (gMG).

Detailed Description: Participants have the option to enroll in an Open-label Extension (OLE) Period to receive ALXN1830 up to 58 weeks (including follow-up period).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Clinical Study Site, Phoenix, Arizona, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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