clinical trial · NCT06479863
Efficacy and Safety of Pozelimab and Cemdisiran Combination Therapy in Patients With Sporadic Inclusion Body Myositis
Austin Neuromuscular Center·early phase1·recruiting·n = 10
Sporadic Inclusion Body Myositis (sIBM)Idiopathic Inflammatory MyopathiesPozelimab/Cemdisiran
brief summary
To evaluate the efficacy of Pozelimab/Cemdisiran combination therapy in patients with sIBM
started
Aug 8, 2024
primary completion
May 30, 2027
completion
Aug 30, 2027
last updated
Jan 16, 2026
detailed description
This is a pilot study of 10 patients to receive Pozelimab 200mg/Cemdisiran 200 mg SC injections every 4 weeks for 104 weeks. SC injections will be administered by the study staff and the patient will be monitored for 30 minutes after the initial first injection. During the remainder of the study, injections can be administered at home by the patient or caregiver after injection training provided by the study staff. Designated persons will be observed to confirm their ability to perform the injections.
The dosing window of the study treatment is within ±7 days from the scheduled dose date.
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol