Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03863080 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Myasthenia Gravis, sponsored by Immunovant Sciences.

Completed
Registry status
Phase 2
Development phase
17
Enrollment target
20
Study locations

NCT03863080: Completed Phase 2 study of Myasthenia Gravis, sponsored by Immunovant Sciences.

NCT03863080 is a Phase 2 study of Myasthenia Gravis that has completed, run by Immunovant Sciences. The registered enrollment target is 17 participants, below the 191-participant average among 32 other Myasthenia Gravis trials with a reported enrollment target (91% lower). The trial reports 20 study locations across 14 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03863080, a Phase 2 study of Myasthenia Gravis, has completed, sponsored by Immunovant Sciences.

COMPLETED
Registry status
Phase 2
Development phase
17 participants
Enrollment target
20
Study locations

Study 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 Myasthenia Gravis patients following treatment with RVT-1401 (also known as IMVT-1401) compared to placebo.

Primary Outcome

An adverse event (AE) is any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment. SAEs were defined as any untoward medical occurrence that, at any dose: resulted in death, was life-threatening, required hospitalization or prolongation of existing hospitalization, resulted in disability/incapacity, was a congenital anomaly/birth defect, or was

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG RVT-1401

Study Locations (20)

California

  • The Neurology Center of Southern California - Carlsbad
  • UC Irvine - MDA ALS and Neuromuscular Center - Orange
  • Care Access Research - Pasadena

New York

  • Dent Institute - Amherst
  • University of Buffalo - Buffalo
  • Hospital for Special Surgery - New York

Ontario

  • London Health Sciences Centre - London
  • Ottawa Hospital Research Institute - Ottawa
  • University Health Network Toronto General Hospital - Toronto

Alabama

  • IMC/Diagnostic and Medical Clinic - Mobile

Arizona

  • Phoenix Neurological Associates - Phoenix

Colorado

  • CSNA - Colorado Springs

Connecticut

  • Yale School of Medicine Department of Neurology - New Haven

Florida

  • Neurological Services of Orlando - Orlando

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2019-05-21
Est. Completion 2020-12-21
Phase Phase 2
Immunovant Sciences

15 total trials

What the finished NCT03863080 record still lists

NCT03863080 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 191-participant average among 32 other Myasthenia Gravis trials with a reported enrollment target (91% lower).

The record links to 1 condition, with Myasthenia Gravis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT03863080 names 20 study sites across 14 states, led by California, New York, Ontario.

Frequently Asked Questions

What is clinical trial NCT03863080 about?

NCT03863080 is a clinical study titled "A Study of RVT-1401 in Myasthenia Gravis (MG) Patients". 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 Myasthenia Gravis patients following treatment with RVT-1401 (also known as IMVT-1401) compa...

What is the current status of trial NCT03863080?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 17 participants. The study started on 2019-05-21. Estimated completion is 2020-12-21.

What conditions does trial NCT03863080 study?

This clinical trial studies the following conditions: Myasthenia Gravis.

What interventions are being tested in trial NCT03863080?

The interventions under investigation include: Placebo (DRUG), RVT-1401 (DRUG).

Who is sponsoring clinical trial NCT03863080?

This trial is sponsored by Immunovant Sciences, which has 15 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03863080 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Myasthenia Gravis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03863080's enrollment target sits among peer trials

17 31st of 32 higher than 2 of 32 other Myasthenia Gravis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Myasthenia Gravis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02090140 · 17 participants · NA

    Microfracture Versus Adipose Derived Stem Cells for the Treatment of Articular Cartilage Defects

  • NCT03317860 · 17 participants · NA

    Improving Measurement and Treatment of Post-stroke Neglect

  • NCT04356469 · 17 participants · Phase 2

    TCR Alpha Beta T-cell Depleted Haploidentical HCT in the Treatment of Non-Malignant Hematological Disorders in Children

  • NCT04414046 · 17 participants · Phase 2

    TCR Alpha Beta T-cell Depleted Haploidentical HCT in the Treatment of Primary Immunodeficiency and Inherited Metabolic Disorders in Children

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03863080, the US trial registry maintained by the National Library of Medicine. NCT03863080 (small enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.