Research outlook

Where CIDP treatment is heading

CIDP · Updated Nov 14, 2026

Chronic inflammatory demyelinating polyneuropathy (CIDP) is an autoimmune disease in which the immune system strips the insulation from nerves, causing weakness and numbness in the arms and legs that builds over months. A few thousand Americans are diagnosed each year. Immunoglobulin infusions, steroids and plasma exchange help most people but often must continue for years. Efgartigimod, an FcRn blocker, became the first new type of treatment in 2024, and drugs that block complement are in phase 3.

  1. Now

    Nov 2026

    A new type of treatmentHappened 61% lower relapse risk

    Efgartigimod cut relapse risk by 61% vs placebo among responders; FDA approved June 2024.

    61%: lower risk of relapse than with placebo.

    Not every drug worksHappened 63.2% worsened with rituximab

    Rituximab (63.2% vs 66.6% worsened) and rozanolixizumab did not beat placebo; riliprubart was stopped in refractory CIDP.

    63.2%: worsened by month 12 with rituximab, vs 66.6% with placebo.

  2. 6 months

    by May 2027

    A second FcRn blockerPossible 61% lower relapse (efgartigimod)

    Janssen's nipocalimab ARISE trial (201 people) finishes December 2026.

    61%: lower risk of relapse than with placebo.

  3. 12 months

    by Nov 2027

    Complement blocker vs immunoglobulinPossible

    Sanofi's VITALIZE (160 people) compares riliprubart with IVIg; due July 2027.

    A C2-blocking antibodyPossible

    argenx's empasiprubart is in two phase 3 trials, one against IVIg (due September 2027) and one against placebo (October 2027).

  4. 3 years

    by late 2029

    More complement blockersPossible

    Dianthus' claseprubart CAPTIVATE (256 people, due December 2028) and Immunovant's imeroprubart (162 people, due August 2028).

  5. 5 years

    by late 2031

    Coming off immunoglobulinLong shot

    The Dutch ReCIX trial (100 people) tests whether rituximab helps people achieve remission; due October 2027, with longer follow-up.

Happened Likely Possible Long shot

The research paths

Established

FcRn blockers

61% lower relapse risk
Details and 1 trialsHide

Lower harmful antibodies; efgartigimod approved, nipocalimab in trials.

WatchARISE.

Mixed

Complement blockers

Details and 5 trialsHide
Early

Inducing remission

63.2% worsened with rituximab
Details and 1 trialsHide

B-cell therapies to get people off long-term treatment.

WatchReCIX.

Borrowed from other conditions

From Myasthenia gravis

Efgartigimod

Approved

An FcRn blocker first approved for myasthenia gravis.

From Myasthenia gravis

Nipocalimab

Phase 2/3

A second FcRn blocker approved for myasthenia.

Open to join now

See every recruiting CIDP trial →

When the trials finish

Completion dates the trials registered. Results usually follow 3 to 12 months later.

2026202720282029203020312032Today
Nipocalimab (ARISE)FcRn blockers
Dec 2026
Jul 2027
Sep 2027
Oct 2027
Oct 2027
ImeroprubartComplement blockers
Aug 2028
Dec 2028

What just happened

Riliprubart halted in refractory CIDP

MOBILIZE.

Rituximab no better than placebo

Brain.

FDA approves efgartigimod for CIDP

ADHERE.

Standard treatment today

How to read this page, and sourcesHow to read this page, and sources

See CIDP trials recruiting now →

Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.