For Patients

For Patients

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Immunovant is currently investigating therapies for people with myasthenia gravis (MG), Graves’ ophthalmopathy (GO), and warm autoimmune hemolytic anemia (WAIHA).

Subcutaneous Delivery

We intend to develop IMVT-1401 as a fixed-dose subcutaneous injection to be administered at home.

Ongoing Trials

Summary information about our ongoing trials is provided below. For more information, please visit www.clinicaltrials.gov

A Study of RVT-1401 in Myasthenia Gravis (MG) Patients

Brief Summary: The purpose of the current study is to assess safety/tolerability and key pharmacodynamic (PD) effects that are considered to be associated with clinical benefit (reduction of total IgG and anti-AChR-IgG) in MG patients following treatment with RVT-1401 (currently known as IMVT-1401) compared to placebo.
Estimated Enrollment: 21 participants
Study Start Date: May 21, 2019
clinicaltrials.gov

A Study of RVT-1401 for the Treatment of Patients With Moderate to Severe Active Graves’ Ophthalmopathy (GO)

Brief Summary: The purpose of the current study is to confirm safety/tolerability and key pharmacodynamic (PD) effects that are considered to drive clinical benefit in GO patients.
Estimated Enrollment: 8 participants
Study Start Date: April 22, 2019
clinicaltrials.gov

A Study of RVT-1401 for the Treatment of Patients with Active, Moderate to Severe Graves’ Ophthalmopathy (GO)

Brief Summary: The purpose of the current study is to assess the efficacy and safety/tolerability of three dose regimens of RVT-1401 (currently known as IMVT-1401) in the treatment of active, moderate to severe GO patients. In addition, the study is designed to characterize the effect of RVT-1401 exposure on reduction in anti-TSHR IgG.
Estimated Enrollment: 77 participants
Study Start Date: July 23, 2019
clinicaltrials.gov

Contact Info

If you would like to learn more about our clinical trials, please contact clinicaltrials@immunovant.com