A Study to Assess the Efficacy and Safety of Empasiprubart in Adults With CIDP

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
Sponsorargenx

About this trial

The main purpose of this study is to demonstrate the efficacy and safety of empasiprubart in adults with CIDP. The study consists of a part A where participants will either receive empasiprubart or placebo for 24 weeks (6 months). Following part A, participants will enter part B in which all participants will receive empasiprubart for 96 weeks (24 months).

More information can be found here: https://clinicaltrials.argenx.com/emnergize

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Meets criteria for CIDP based on EAN/PNS Task Force CIDP guidelines, second revision (2021)

Has either typical CIDP or 1 of the following CIDP variants: motor CIDP (including motor-predominant CIDP), multifocal CIDP (also known as Lewis-Sumner syndrome), focal CIDP, or distal CIDP

Has residual disability and active disease

Has not received previous treatment for CIDP; or has stopped receiving CIDP treatment; or is receiving CIDP treatment (pulsed or oral corticosteroids, immunoglobulins, PLEX, or FcRn inhibitors)

Disqualifiers

Meets the criteria for possible CIDP based on EAN/PNS Task Force CIDP guidelines, second revision (2021)

Sensory CIDP (including sensory-predominant CIDP)

Polyneuropathy of other causes

Clinical diagnosis of systemic lupus erythematosus (SLE)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Empasiprubart IV

    Biological/Vaccine

    Intravenous infusion of empasiprubart

  • Placebo IV

    Other intervention

    Intravenous infusion of placebo

Treatment groups

160 Participants
are divided into 3 treatment groups
Group A: Part A - EmpasiprubartExperimental treatment 1 intervention
Group B: Part A - PlaceboPlacebo comparator 1 intervention
Group C: Part B - EmpasiprubartExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Reduction of ≥1 point compared with baseline in aINCAT score at week 24

The Adjusted Inflammatory Neuropathy Cause and Treatment Disability Score (aINCAT) score is a 10-point scale that covers the functionality of legs and arms. The score varies between 0 and 10 (higher score, worse outcome).

Time frame
Up to 24 weeks

Secondary outcomes

1

Change from baseline in I-RODS centile points score

Inflammatory Rasch-built Overall Disability Scale (I-RODS) assesses the limitations of activities and social participation in patients with inflammatory neuropathies like CIDP. The score ranges from 0 to 100 (higher score, worse outcome).

Time frame
Up to 24 weeks (part A) + 96 weeks (Part B)
2

Change from baseline in MRC-SS at week 24

The Medical Research Council Sum Score evaluates motor strength. Evaluated on 6 muscle groups on each side, the score varies from 0 to 60 (lower score, worse outcome)

Time frame
Up to 24 weeks
3

Change from baseline in grip strength (3-day moving average) in the dominant hand at week 24

Time frame
Up to 24 weeks
4

Time to reduction of ≥1 point from baseline in aINCAT score

The Adjusted Inflammatory Neuropathy Cause and Treatment Disability Score (aINCAT) score is a 10-point scale that covers the functionality of legs and arms. The score varies between 0 and 10 (higher score, worse outcome).

Time frame
Up to 24 weeks

Other outcomes

Sponsors and contacts

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