About this trial
Stiff Person Syndrome (SPS) is a rare autoimmune disorder, characterized by: a) incapacitating diffuse muscle stiffness prominent in the axial, abdominal and thoracolumbar paraspinal muscles leading to hyperlordosis, difficulty turning and bending; b) painful muscle spasms precipitated by external stimuli with difficulty performing routine daily activities; and c) slow freezing gait with frequent falls and need for walking aids leading to disability. SPS is due to impaired inhibitory GABAergic neurotransmission associated with high-titer IgG antibodies against Glutamic Acid Decarboxylase (GAD), the rate-limiting enzyme for the synthesis of the inhibitory gammaaminobutyric acid (GABA). Although SPS patients respond to IVIg based on the PI's controlled study (NEJM 2001), several patients do not improve, or their response is modest and declines over time, as documented in a longitudinal study of 36 patients followed in our Jefferson clinic; because another controlled study we performed with Rituximab was negative and SPS is a progressive disease, new therapies are needed. Efgartigimod is an FcRn inhibitor that enhances the catabolism of circulating IgG; its subcutaneous, self-administered form, HYTRULO, has been effective and FDA-approved in patients with myasthenia gravis or CIDP poorly responding to IVIg. There is evidence that patients with myasthenia who also had SPS, Hytrulo not only helped their myasthenia but the SPS also impressively improved.
The present study is an investigator- initiated, double-blind, placebo controlled, cross-over, trial in 26 GAD-positive SPS patients poorly responding to available therapies. Patients will be recruited from the large number of patients seen and referred to the PI who is known for his work in SPS and has conducted the 2 previous controlled trials. Although Hytrulo is approved as selfadministered subcutaneous drug with pre-refilled syringes, in this study will be given by a contracted home infusion company once a week to ensure convenience, safety and validity. Patients will be randomized by the Jefferson Pharmacy to receiving Hytrulo or identical hyaluronidase-containing placebo for 3 months; then they will be crossed-over to placebo/Hytrulo for another 3 months. Efficacy will be based on one primary endpoint, the stiffness index, previously validated by the PI, and on two also validated secondary endpoints of time to walk and excitability index. This design provides the statistical power to objectively assess a 25-50% or greater change and objectively determine if Hytrulo offers meaningful benefits in reducing stiffness and spasms, improving gait and increasing quality of life in SPS patients poorly responding to current therapies.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
26 patients age 25-80 with typical SPS as per Dalakas's diagnostic criteria (1,2) poorly or partially responding to IVIg or rituximab with declining benefits, exhibiting significant symptomatology of stiffness, painful muscle spasms, and impaired walking ability will be selected. All enrolled patients will be GAD-ab or Glycin-receptor-antibody-positive and will continue receiving the non-immunosuppressive symptomatic drugs, such as diazepam, gabapentin, or baclofen.
All selected patients will be among the large number we currently follow in our outpatient clinic or among those being continuously referred for a second opinion or better therapies when unresponsive to current drugs.
All patients should be able to provide informed consent and willing to travel for scheduled protocol visits.
Disqualifiers
Patients will be excluded if: a) have minimal disease, and less than 1 stiffness index; b) have very severe disease unresponsive to all therapies or non-ambulatory; and c) have paraneoplastic SPS.
Trial design
Crossover
Treatments tested in this trial
VYVGART Hytrulo
DrugThese patients will receive 1000 mg efgartigimod PH20 SC (VYVGART Hytrulo), every week for 12 weeks (as per Hytrulo's therapeutic guidelines)
Hytrulo-placebo (consisting of Hyaluronidase)
DrugHytrulo-placebo (consisting of Hyaluronidase)
Treatment groups
Trial outcomes
Primary outcomes
Stiffness Index
The primary endpoint, and has been validated in SPS and used in two previous Dalakas's controlled trials. Change in Stiffness Index measured at monthly visits.
Secondary outcomes
T25-FW (time to walk 25 feet)
Assessments will be based on the monthly Clinic exams from baseline to Week 12 (monthly visits #1-4,) and after the cross-over from Week 12 to 24 (visits# 5-7).
Modified Rankin Scale
Assessments will be based on the monthly Clinic exams from baseline to Week 12 (monthly visits #1-4,) and after the cross-over from Week 12 to 24 (visits# 5-7).
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