Batoclimab for Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Enrolling by invitation at 29 trial locations
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Immunovant Sciences GmbH
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores the long-term safety of batoclimab, a treatment for Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP), a condition affecting the nerves and causing weakness. Participants will receive a weekly injection of batoclimab for up to a year. The study is open to those who have already completed a related batoclimab study. Participants should not have any other major health issues that could interfere with the study. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to important findings.

Do I have to stop taking my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the study team or your doctor.

Is there any evidence suggesting that batoclimab is likely to be safe for humans?

Research has shown that batoclimab has been tested for safety in treating other conditions. In one study with adults who have myasthenia gravis (MG), researchers compared batoclimab to a placebo to assess its safety. The study found that batoclimab was generally well-tolerated, with most participants not experiencing serious problems. Some side effects were reported, but they were mostly mild to moderate.

For those considering joining the trial for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), this information suggests that batoclimab is relatively safe based on past research. However, as with any treatment, individual experiences can differ, so discussing any concerns with the trial team is important.12345

Why do researchers think this study treatment might be promising for CIDP?

Unlike the standard treatments for Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP), which often include corticosteroids or immunoglobulin therapy, Batoclimab takes a different approach. It targets the neonatal Fc receptor (FcRn), which plays a key role in regulating the immune system and antibody levels. By interfering with this receptor, Batoclimab may reduce the harmful antibodies that attack the nervous system in CIDP. Researchers are excited about Batoclimab because this specific mechanism could offer a more targeted treatment, potentially leading to fewer side effects and improved efficacy compared to existing therapies.

What evidence suggests that batoclimab might be an effective treatment for CIDP?

Studies have shown that batoclimab effectively treats conditions similar to chronic inflammatory demyelinating polyneuropathy (CIDP). For instance, research on myasthenia gravis, a related autoimmune disorder, showed significant improvement in patient symptoms. This is encouraging for CIDP because both conditions involve the immune system attacking the body's nerves. Early findings suggest batoclimab can help reduce these attacks, potentially improving nerve function and relieving symptoms. Although more research is needed specifically for CIDP, these initial results offer hope for its effectiveness. Participants in this trial will receive batoclimab to further evaluate its potential benefits for CIDP.12345

Are You a Good Fit for This Trial?

This trial is for adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) who have already completed the Study IMVT-1401-2401. Participants should be able to receive weekly injections and commit to a year-long study, including follow-up.

Inclusion Criteria

Female participants must agree not to donate eggs throughout the study and for 90 days after the final study treatment administration
Any participant who has completed Study IMVT-1401-2401
Agree not to participate in another interventional study while on treatment
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Exclusion Criteria

Participant has any medical condition (acute or chronic illness) or psychiatric condition, including autoimmune disease or neurologic disease other than CIDP, or known history of drug or alcohol abuse that, in the opinion of the Investigator, could jeopardize the participant's ability to participate in this study, compromise accurate assessment of CIDP symptoms or otherwise interfere with the course and conduct of the study
Participant intends to have a live vaccination during the course of the study or within 7 weeks following the final dose of batoclimab
Participant has an ongoing SAE or a medical condition in the IMVT-1401-2401 study that the Investigator considers putting the participant at a significantly increased risk of participating in Study IMVT-1401-2402
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive 340 mg of batoclimab subcutaneously once weekly for up to 52 weeks

52 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks
1 visit (in-person) approximately 28 (± 7) days after the Week 52 or ET Visit

What Are the Treatments Tested in This Trial?

Interventions

  • Batoclimab
Trial Overview The trial is testing the long-term safety of Batoclimab, given as a subcutaneous injection once a week for up to one year. The focus is on how well participants tolerate this treatment over an extended period.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: BatoclimabExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Immunovant Sciences GmbH

Lead Sponsor

Trials
12
Recruited
1,400+

Citations

Roivant Announces Positive Results for Batoclimab ...Pivotal study in MG met primary endpoint of change from baseline in MG-ADL in AChR+ population at 12 weeks, with a 5.6 point improvement in ...
Immunovant Announces Positive Results for Batoclimab ...Pivotal study in MG met primary endpoint of change from baseline in MG-ADL in AChR+ population at 12 weeks, with a 5.6 point improvement in ...
IMVT-1402 Evaluated for Use in Patients With CIDPBatoclimab showed positive results in studies of myasthenia gravis ... chronic inflammatory demyelinating polyneuropathy (CIDP) studies.
An Open-Label Extension Study of Batoclimab in Adult ...This is an open-label extension (OLE) study designed to evaluate the long-term safety and tolerability of batoclimab in participants with CIDP who have ...
MVT-1401-2401 Study of Batoclimab Treatment in Adult ...MVT-1401-2401 study wants to learn more about the safety and effectiveness of an investigational drug called batoclimab to see if it could help CIDP patients ...
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