Immunovant Sciences GmbH: Clinical Trials

19 trials sponsored by Immunovant Sciences GmbH, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

6 terminated, 5 completed, 4 recruiting, 3 active not recruiting. 14 Phase 2, 5 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 214Terminated 4, Active not recruiting 3, Completed 3, Recruiting 3, Enrolling by invitation 1
Phase 35Completed 2, Terminated 2, Recruiting 1

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Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Long-Term Extension Study of IMVT-1402 in Adult Participants With Graves' Disease (GD)
IMVT-1402 - Graves' Disease
Phase 2Enrolling by invitationImmunovant Sciences GmbH3722026-01-262026-09-29
An Open-Label Extension Study of Batoclimab in Adult Participants With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Batoclimab - Chronic Inflammatory Demyelinating Polyneuropathy
Phase 2TerminatedImmunovant Sciences GmbH262025-08-282026-08-11
Efficacy and Safety of IMVT-1402 in Adult Participants With Primary Sjogren's Disease With Moderate to Severe Systemic Disease Activity
IMVT-1402, Placebo - Primary Sjögren's Syndrome
Phase 2Active not recruitingImmunovant Sciences GmbH1802025-06-302026-09-10
A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves' Disease
IMVT-1402, Placebo - Graves' Disease
Phase 2RecruitingImmunovant Sciences GmbH2102025-06-192026-08-25
Study to Assess the Efficacy and Safety of IMVT-1402 in Participants With Mild to Severe Generalized Myasthenia Gravis
IMVT-1402, Placebo - Generalized Myasthenia Gravis
Phase 3RecruitingImmunovant Sciences GmbH2312025-05-272026-07-30
Imeroprubart in Adult Participants With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Imeroprubart, Placebo - Chronic Inflammatory Demyelinating Polyneuropathy
Phase 2RecruitingImmunovant Sciences GmbH1622025-03-182026-09-30
A Study to Assess the Safety, Tolerability, and Efficacy of IMVT-1402 in Participants With Cutaneous Lupus Erythematosus (CLE)
IMVT-1402, Placebo - Subacute Cutaneous Lupus Erythematosus, Chronic Cutaneous Lupus Erythematosus
Phase 2Active not recruitingImmunovant Sciences GmbH562025-02-192026-08-28
A Study to Evaluate the Efficacy, Safety, and Tolerability of IMVT-1402 in Adult Participants With Active, Difficult to Treat Rheumatoid Arthritis
IMVT-1402, Placebo - Rheumatoid Arthritis
Phase 2Active not recruitingImmunovant Sciences GmbH1202025-01-102026-04-22
A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves' Disease
IMVT-1402, Placebo - Graves' Disease
Phase 2RecruitingImmunovant Sciences GmbH2402024-12-172026-08-25
A Proof-of-Concept Study to Assess Batoclimab in Participants With Graves' Disease
IMVT-1401 (batoclimab) - Graves Disease
Phase 2CompletedImmunovant Sciences GmbH322023-05-152026-08-13
Study to Assess Batoclimab in Participants With Active Thyroid Eye Disease
Batoclimab, Placebo - Thyroid Eye Disease
Phase 3CompletedImmunovant Sciences GmbH862023-01-052026-04-01
To Assess Efficacy and Safety of Batoclimab in Adult Participants With Active CIDP
Batoclimab 680 milligrams (mg) subcutaneous (SC) weekly, Batoclimab 340 mg SC weekly, Placebo - Chronic Inflammatory Demyelinating Polyneuropathy
Phase 2TerminatedImmunovant Sciences GmbH942022-12-152026-08-11
Study to Assess Batoclimab in Participants With Active Thyroid Eye Disease
Batoclimab, Placebo - Thyroid Eye Disease
Phase 3CompletedImmunovant Sciences GmbH1142022-11-232025-12-03
Extension Study to Assess Batoclimab in Participants With Thyroid Eye Disease
Observational cohort study, Batoclimab - Thyroid Eye Disease
Phase 3TerminatedImmunovant Sciences GmbH1092022-11-062026-04-29
Phase 3 Study to Assess the Efficacy and Safety of Batoclimab as Induction and Maintenance Therapy in Adult Participants With Generalized Myasthenia Gravis
Batoclimab 680 mg SC weekly, Batoclimab 340 mg SC weekly, Matching Placebo SC - Generalized Myasthenia Gravis
Phase 3TerminatedImmunovant Sciences GmbH2332022-06-272026-09-14
To Assess the Efficacy and Safety of RVT-1401 in the Treatment of Warm Autoimmune Hemolytic Anemia (ASCEND-WAIHA).
RVT-1401 680 mg/weekly, RVT-1401 340 mg/weekly - Warm Autoimmune Hemolytic Anemia
Phase 2TerminatedImmunovant Sciences GmbH52020-08-112022-07-28
ASCEND GO-2: Study of RVT-1401 for the Treatment of Participants With Active, Moderate to Severe Graves' Ophthalmopathy ( GO )
RVT-1401 (Administered via subcutaneous injection), Placebo (Administered via subcutaneous injection) - Graves' Ophthalmopathy (GO)
Phase 2TerminatedImmunovant Sciences GmbH652019-07-232022-09-22
A Study of RVT-1401 in Myasthenia Gravis (MG) Patients
RVT-1401, Placebo - Myasthenia Gravis
Phase 2CompletedImmunovant Sciences GmbH172019-05-212023-12-20
Study of RVT-1401 for the Treatment of Patients With Moderate to Severe Active Graves' Ophthalmopathy (GO)
RVT-1401 - Graves' Ophthalmopathy
Phase 2CompletedImmunovant Sciences GmbH72019-04-222022-01-24

Conditions studied

Autoimmune Diseases (7)  ·  Graves Ophthalmopathy (5)  ·  Graves Disease (4)  ·  Myasthenia Gravis (3)  ·  Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (3)  ·  Hyperthyroidism (2)  ·  Arthritis, Rheumatoid (1)  ·  Lupus Erythematosus, Cutaneous (1)  ·  Lupus Erythematosus, Discoid (1)

Interventions

Injections, Subcutaneous (1)

Countries

United States (17)  ·  Germany (13)  ·  Poland (13)  ·  Spain (13)  ·  United Kingdom (13)  ·  Italy (11)  ·  Georgia (9)  ·  Hungary (9)  ·  Argentina (8)  ·  Canada (8)  ·  Greece (7)  ·  Romania (7)  ·  Belgium (6)  ·  Bulgaria (6)  ·  Serbia (6)

Results publications

PMID 38268752

NIH funding

2025 (2)