Clinical trial · Interventional
Study of Telitacicept in Generalized Myasthenia Gravis
A Multi-center, Randomized, Double-blind, Placebo-controlled, Phase III Study of Telitacicept in Patients With Generalized Myasthenia Gravis
NCT05737160CI-TRIAL-00090104completedPhase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the efficacy and safety of Telitacicept in the treatment of patients with generalized myasthenia gravis.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Myasthenia Gravis, Generalized | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Placebo | Drug | — | UNRESOLVED |
| Telitacicept | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Telitacicept
- description
- Participants will receive subcutaneous Telitacicept 240 mg once a week for a total of 48 doses in addition to MG SoC.
- interventionNames
- Biological: Telitacicept
- type
- PLACEBO_COMPARATOR
- label
- Placebo
- description
- Participants will receive subcutaneous placebo once a week for a total of 24 doses (part A) and then weekly subcutaneous Telitacicept 240 mg for 24 doses (part B) in addition to MG SoC.
- interventionNames
- Drug: Placebo
Primary outcomes (1)
- measure
- Change from baseline in MG-ADL
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Written informed consent provided; 2. Male or female patients aged 18-80 years; 3. Diagnosis with generalized myasthenia gravis; 4. MGFA Class II, III, or IVa; 5. AChR-Ab or MuSK-Ab positive; 6. A total MG-ADL score of ≥ 6 with less than 50% of the total score due to ocular symptoms; 7. QMG ≥ 8, with ≥ 4 items score at least 2; 8. Have been on a stable MG SoC regimen. Exclusion Criteria: 1. Patients with autoimmune diseases other than MG; 2. Abnormal laboratory results; 3. Use of immunosuppressants other than standard therapy within 1 month before randomization; 4. Use of biologic agents targeting therapy, such as Rituximab or complement C5 inhibitors, within 6 months before randomization; 5. Use of neonatal Fc receptor (FcRn) antagonists, intravenous immunoglobulin (IVIg), or plasmapheresis within 2 months before randomization; 6. Significant cardiovascular disease, liver, kidney, respiratory, endocrine or hematologic disease, or other medical conditions that, in the opinion of the investigator, would preclude the subject's participation in the study or require hospitalization during the study; 7. Acute or chronic infection requiring treatment; 8. Current active hepatitis; 9. HIV antibody positive; 10. Patients currently suffering from thymoma-associated immunodeficiency syndrome (Good's syndrome) or who underwent thymectomy within 6 months before screening; 11. Received or plan to receive any live vaccine within 3 months prior to randomization; 12. Patients with malignant tumors; 13. Allergy to biological products of human origin; 14. Participation in any clinical trial 28 days prior to randomization or within 5 times the half-life of an investigational drug (whichever is longer); 15. Pregnant or lactating women, and those intending to become pregnant during the trial; 16. Patients considered unsuitable by the investigator to participate in the trial (e.g., patients with severe mental disorders); Note: Other protocol defined Inclusion/Exclusion criteria may apply.
References
Publications (0)
Data not yet available
No reference posted for this study.