Study to Assess the Efficacy and Safety of IMVT-1402 in Participants With Mild to Severe Generalized Myasthenia Gravis
Immunovant Sciences GmbH · NCT07039916
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–80 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 231
- US sites recruiting
- 48
- Study start
- May 27, 2025
- Record last updated
- July 30, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of the study is to assess the efficacy, safety and tolerability of IMVT-1402 in adult participants with mild to severe generalized myasthenia gravis.
Being studied: IMVT-1402; IMVT-1402; Placebo; IMVT-1402
Conditions: Generalized Myasthenia Gravis
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Participants with the ability to understand the requirements of the trial, provide written informed consent, and comply with the trial protocol procedures.
- Have mild to severe gMG by Myasthenia Gravis Foundation of America (MGFA) classification of Class II, III, or IVa at the Screening Visit
- Have an MG activities of daily living (MG-ADL) score of ≥ 6 at the Screening Visit and Baseline Visit (Day 1)
Additional inclusion criteria are defined in the protocol.
Exclusion Criteria
- Have experienced myasthenic crisis within 12 weeks prior to the Screening Visit.
- Have had a thymectomy performed \< 6 months prior to the Screening Visit or have a planned thymectomy during the study
- Have any active or untreated malignant thymoma
Additional exclusion criteria are defined in the protocol.
Recruiting US locations
Site Number - 1056
Huntsville, AL 35801
Site Number - 1041
Mobile, AL 36604
Site Number - 1017
Phoenix, AZ 85028
Site Number - 1025
Scottsdale, AZ 85251
Site Number - 1042
Tucson, AZ 85718
Site Number - 1010
Carlsbad, CA 92011
Site Number - 1028
Irvine, CA 92697
Site Number - 1023
Los Angeles, CA 90033
Site Number - 1029
Rancho Mirage, CA 92270
Site Number - 1004
San Francisco, CA 94143
Site Number - 1027
Fort Collins, CO 80528
Site Number - 1001
New Haven, CT 06510
Site Number - 1024
Washington D.C., DC 20010
Site Number - 1006
Clearwater, FL 33761
Site Number - 1037
Ormond Beach, FL 32174
Site Number - 1002
Port Charlotte, FL 33952
Site Number - 1050
Rockledge, FL 32955
Site Number - 1007
Tampa, FL 33612
Site Number - 1014
Atlanta, GA 30329
Site Number - 1043
Augusta, GA 30912
Site Number - 1054
Schaumburg, IL 60173
Site Number - 1022
Lexington, KY 40536-0284
Site Number - 1032
Nicholasville, KY 40356
Site Number - 1046
New Orleans, LA 70121
Site Number - 1049
Foxborough, MA 02035
Site Number - 1026
Detroit, MI 48201
Site Number - 1005
East Lansing, MI 48824
Site Number - 1018
Omaha, NE 68198
Site Number - 1019
Totowa, NJ 07512
Site Number - 1036
New York, NY 10021
Site Number - 1034
New York, NY 10065
Site Number - 1020
Chapel Hill, NC 27599
Site Number - 1013
Durham, NC 27710
Site Number - 1044
Raleigh, NC 27607
Site Number - 1038
Cincinnati, OH 45221
Site Number - 1045
Oklahoma City, OK 73104
Site Number - 1011
Yukon, OK 73099
Site Number - 1031
Eugene, OR 97477
Site Number - 1030
Charleston, SC 29425
Site Number - 1015
Charleston, SC 29486
Site Number - 1021
Memphis, TN 38120
Site Number - 1003
Dallas, TX 75206
Site Number - 1047
Denton, TX 76208
Site Number - 1057
Houston, TX 77054
Site Number - 1048
Lubbock, TX 79414
Site Number - 1009
Charlottesville, VA 22903
Site Number - 1040
Richmond, VA 23298
Site Number - 1035
Greenfield, WI 53228
Study contacts (from the official record)
- Central Study Contact · 18007970414 · clinicaltrials@immunovant.com
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