The MIGHT Trial - An Exploratory Clinical Trial of IVIG in Anti-HMGCR Immune Mediated Necrotizing Myopathy

The University of Alabama at Birmingham

Status and phase: Enrolling; Phase 2

Conditions: Anti-3-hydroxy-3-methylglutaryl-CoA Reductase (HMGCR) Immune-Mediated Necrotizing Myopathy

Treatments: Biological: Intravenously administered pooled human immunoglobulin (IVIG)

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT06599697

1R21AR083566-01A1 (U.S. NIH Grant/Contract)

300013467

Details and patient eligibility

About

This is a randomized, placebo-controlled, double blinded phase 2 exploratory clinical trial of intravenously administered pooled human immunoglobulin (IVIG) in anti-3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) immune mediated necrotizing myopathy (IMNM). Planned enrollment is 12 individuals with active anti-HMGCR IMNM meeting inclusion and exclusion criteria. Assuming 20% drop-out, the investigators anticipate 10 participants will complete all study assessments. Enrolled participants will be randomized 1:1 to either IVIG 2g/kg or placebo (0.9% sodium chloride at equivalent volume) at weeks 0, 4, and 8. The primary efficacy and co-primary safety and tolerability endpoints will be assessed at week 12. After the randomized phase of the trial, all participants will be offered to continue on to an open-label extension phase in which participants will receive IVIG at weeks 12, 16, and 20. Participants will then return at week 24 for a final non-infusion visit to reassess safety, tolerability, and efficacy outcome.

Enrollment: 12 estimated patients

Sex: All

Ages: 16+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age > 16 years
• Anti-HMGCR antibody positive
• MMT-8 score < 142 (range 0-160)
• Serum CK > 5x upper limit of normal
• Anti-HMGCR IMNM disease duration < 36 months at screening
• No moderate or severe respiratory or swallowing dysfunction due to anti-HMGCR IMNM at screening
• No history of dermatomyositis rash
• Must reside in a state with a participating research site

Exclusion criteria

• Oral glucocorticoid (GC) daily dose > 15mg at screening

• Change in oral GC dose < 2 weeks prior to screening

• Prior IVIG treatment for anti-HMGCR IMNM

  ->1 oral conventional synthetic DMARD (e.g. methotrexate, mycophenolate mofetil, azathioprine) use at screening

• Change in concomitant DMARD dose < 4 weeks prior to screening

• Rituximab < 6 months prior to screening

• Plasma exchange, cyclophosphamide, or biologic immunosuppressive medication < 3 months prior to screening

• Use of statin medication at screening

• History of anaphylactic reaction to IVIG

• History of angina pectoris, myocardial infarction, transient ischemic attack, or stroke < 12 months prior to screening

• Females of child-bearing potential who are pregnant, breastfeeding, or are unwilling to practice a highly effective method of contraception during the study

• Wells Criteria for DVT score of 2 or more at screening

• Wells Criteria for PE score of 4 or more at screening

• Weight >120kg

• History of cancer (excluding non-melanomatous skin cancer) < 5 years prior to screening

• History of pulmonary embolism or deep venous thromboembolism < 3 years prior to screening

• History of hyperviscosity or hypercoagulable state

• Currently receiving anti-coagulation therapy (vitamin K antagonists, non-vitamin K oral anticoagulants [e.g. dabigatran, rivaroxaban, apixaban], parenteral anticoagulants [e.g. fondaparinux]. Note that oral anti-platelet agents are allowed (e.g. aspirin, clopidogrel, ticlopidine).

• Glomerular filtration rate (GFR) <60mL/min at the time of screening

• Any medical condition which, in the investigator's judgment, makes participation in the clinical trial unadvisable or which would interfere with evaluation of the study treatment.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

12 participants in 2 patient groups

Intravenously Administered Pooled Human Immunoglobulin (IVIG)

Experimental group

Description:

Participants will receive intravenously administered pooled human immunoglobulin (IVIG) 2g/kg every 4 weeks for 24 weeks.

Treatment:

Biological: Intravenously administered pooled human immunoglobulin (IVIG)

Placebo

No Intervention group

Description:

Participants will receive an infusion of 0.9% sodium chloride solution every 4 weeks for 16 weeks at equivalent volume to corresponding IVIG weight-based dose.