Myasthenia Gravis Clinical Trials

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OCTAGON: A Phase 4, Single Arm Study to Investigate Oral Corticosteroid Tapering in Adult Patients With Generalized Myasthenia Gravis Treated With Ravulizumab

Status: Recruiting
Location: See all (12) locations...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This is a prospective, multicenter single arm study designed to evaluate the effectiveness and safety of a predefined oral corticosteroids (OCS) tapering schedule to reduce OCS use in adult participants with acetylcholine receptor positive (AChR+) generalized myasthenia gravis (gMG) being treated with intravenous ravulizumab.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Aged greater than 18 years and male or female

• Clinical diagnosis of gMG

• Receiving ravulizumab treatment prior to enrollment

• Receipt of OCS therapy equivalent to a daily dose ≥ 7.5 mg of prednisone/prednisolone for ≥ 4 continuous weeks directly preceding enrollment

• A participant of childbearing potential must have a negative highly sensitive pregnancy test (serum or urine, as required by local regulations) taken at Screening before OCS tapering begins.

• Willing to sign informed consent

Locations
United States
Illinois
Research Site
NOT_YET_RECRUITING
Chicago
Research Site
NOT_YET_RECRUITING
Schaumburg
North Carolina
Research Site
RECRUITING
Raleigh
New Jersey
Research Site
NOT_YET_RECRUITING
Neptune City
Tennessee
Research Site
NOT_YET_RECRUITING
Knoxville
Other Locations
Germany
Research Site
NOT_YET_RECRUITING
Bochum
Italy
Research Site
NOT_YET_RECRUITING
Milan
Research Site
NOT_YET_RECRUITING
Naples
Research Site
NOT_YET_RECRUITING
Rome
Japan
Research Site
NOT_YET_RECRUITING
Ibaraki
Research Site
NOT_YET_RECRUITING
Kitakyushu-shi
Research Site
NOT_YET_RECRUITING
Kumamoto
Contact Information
Primary
Alexion Pharmaceuticals, Inc. (Sponsor)
clinicaltrials@alexion.com
1-855-752-2356
Time Frame
Start Date: 2026-03-04
Estimated Completion Date: 2027-08-27
Participants
Target number of participants: 75
Treatments
Experimental: Oral Corticosteroid Tapering Schedule
During the tapering period, participant will follow an Oral Corticosteroid tapering schedule until OCS tapering is complete
Related Therapeutic Areas
Sponsors
Leads: Alexion Pharmaceuticals, Inc.

This content was sourced from clinicaltrials.gov