A Study to Examine the Efficacy and Safety of Pozelimab and Cemdisiran Combination Therapy in Adult Patients With Symptomatic Generalized Myasthenia Gravis

• Status: Not yet recruiting
• Trial end date: 2027-02-26
• Target enrollment: 0
• Participant gender: All

Summary

The primary objective is:

To evaluate the effect of pozelimab + cemdisiran on daily functioning that is impacted by signs and symptoms in patients with symptomatic generalized myasthenia gravis (gMG)

The secondary objectives of the study are:

• To evaluate the effect of pozelimab + cemdisiran (ie, combination) and cemdisiran monotherapy on:

• Clinician-assessed signs of myasthenia gravis (MG) and muscle strength

• Daily functioning that is impacted by signs and symptoms in patients with symptomatic gMG (cemdisiran monotherapy only).

• Proportion of patients with improvements in daily function that is impacted by signs and symptoms of MG

• Proportion of patients that have improvements in clinician-assessed signs of MG and muscle strength

• Health related quality of life

• Proportion of patients with minimal MG symptoms

• Patient- and clinician-reported signs and symptoms of MG

• To evaluate the safety and tolerability of pozelimab + cemdisiran and cemdisiran monotherapy

• To assess the concentration of total pozelimab in serum

• To assess the concentrations of cemdisiran and its metabolites in plasma

• To assess the immunogenicity of pozelimab

• To assess the immunogenicity of cemdisiran

• To study the effect of pozelimab + cemdisiran and cemdisiran monotherapy on complement activation

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Regeneron Pharmaceuticals

Criteria

Key Inclusion Criteria:

1. Male or female patients ≥18 years of age at screening (or ≥ legal age of adulthood based on local regulations, whichever is older)

2. Patient with documented diagnosis of myasthenia gravis (MG) based on medical history and supported by previous evaluations as described in the protocol

3. Documented prior history of positive serologic test or a positive result during screening of anti-acetylcholine receptor (AChR) antibodies or anti-LRP4 antibodies.

4. Myasthenia Gravis Foundation of America (MGFA) Clinical Classification Class II to IVa at screening

5. Myasthenia Gravis-Activities of Daily Living (MG-ADL) score ≥6 at screening. Ocular items should not contribute more than 50% of MG-ADL total score

6. Currently receiving an acetylcholinesterase inhibitor or documented reason for not using acetylcholinesterase inhibitor therapy per investigator 7. Currently receiving an immunosuppressive therapy (IST) for MG, or documented reason why the patient is not taking an IST per investigator

8. If currently receiving an IST, not anticipated to have IST dosage changed before randomization or during double-blind treatment period (DBTP).

Key Exclusion Criteria:

1. Patients with a positive serologic test for antibodies to muscle specific tyrosine kinase (MuSK) during screening

2. History of thymectomy within 12 months prior to screening or planned during the study

3. History of malignant thymoma (patients with stage 1 may be enrolled), or history of cancer within the past 5 years, except for adequately treated basal cell skin cancer, squamous cell skin cancer, or in situ cervical cancer

4. Myasthenic crisis or Myasthenia Gravis Foundation of America (MGFA) Class V within 1 month of screening

5. No documented meningococcal vaccination within 5 years prior to screening visit unless vaccination will be administered during the screening period and prior to initiation of study treatment

6. Known contraindication to meningococcal vaccines (group ACWY conjugate and group B vaccines) as described in the protocol

7. Patients who require antibiotics for meningococcal prophylaxis and have a contraindication, warning, or precaution precluding the use of penicillin class and penicillin-alternative antibiotics planned to be used for prophylaxis, or a history of intolerance leading to the discontinuation of these antibiotics

8. Positive hepatitis B surface antigen or hepatitis C virus ribonucleic acid (RNA) during screening. NOTE: Cases with unclear interpretation should be discussed with the medical monitor

9. History of HIV infection

NOTE: Other protocol-defined Inclusion/ Exclusion Criteria apply