Ireland
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Priya Life Science Sponsor trial record
Sponsor · clinical trials

Immunovant Sciences clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our UK, USA, Poland, Spain, Germany, Italy, Czechia, Australia, Netherlands, Belgium, Denmark, Brazil, Mexico, Canada, South Korea, Israel, Ireland, Austria, Norway, Portugal, Turkey, Japan and EU (CTIS) registers with Immunovant Sciences as lead sponsor. Synced 12 Nov 2026
9Current trials
4Recruiting now
1Drug in these trials
23Trial registers
At a glance

Immunovant Sciences is the lead sponsor of 9 current clinical trials in our UK, USA, Poland, Spain, Germany, Italy, Czechia, Australia, Netherlands, Belgium, Denmark, Brazil, Mexico, Canada, South Korea, Israel, Ireland, Austria, Norway, Portugal, Turkey, Japan and EU (CTIS) registers. 4 are recruiting patients now. The most common phase is Phase 2. The drugs named most often in its trials are IMVT-1402. The most-studied condition is Graves' Disease.

ClinicalTrials.gov trials by status

  • Recruiting450%
  • Active, closed338%
  • By invitation113%

Trials by phase

  • Phase 2788%
  • Phase 3113%
01

Clinical trials sponsored by Immunovant Sciences

8 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Imeroprubart in Adult Participants With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
NCT07032662 · Chronic Inflammatory Demyelinating Polyneuropathy
Phase 2 Recruiting 2025-03 Ireland, UK, USA, Germany, Spain, Italy, Netherlands, Belgium, Denmark, Poland, Austria, Norway, Portugal, Turkey, Brazil, Mexico, Australia
Study to Assess the Efficacy and Safety of IMVT-1402 in Participants With Mild to Severe Generalized Myasthenia Gravis
NCT07039916 · Generalized Myasthenia Gravis
Drug: IMVT-1402
Phase 3 Recruiting 2025-05 UK, USA, Germany, Spain, Italy, Denmark, Poland, Czechia, Mexico
A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves' Disease
NCT07018323 · Graves' Disease
Drug: IMVT-1402
Phase 2 Recruiting 2025-06 UK, USA, Spain, Italy, Netherlands, Poland, Czechia, Brazil, Japan, South Korea, Australia, Israel
A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves' Disease
NCT06727604 · Graves' Disease
Drug: IMVT-1402
Phase 2 Recruiting 2024-12 UK, USA, Germany, Spain, Italy, Belgium, Poland
A Long-Term Extension Study of IMVT-1402 in Adult Participants With Graves' Disease (GD)
NCT07286006 · Graves' Disease
Drug: IMVT-1402
Phase 2 By invitation 2026-01 UK, USA, Poland, Czechia, South Korea, Australia, Israel
A Study to Assess the Safety, Tolerability, and Efficacy of IMVT-1402 in Participants With Cutaneous Lupus Erythematosus (CLE)
NCT06980805 · Subacute Cutaneous Lupus Erythematosus, Chronic Cutaneous Lupus Erythematosus
Drug: IMVT-1402
Phase 2 Active, closed 2025-02 UK, USA, Germany, Spain, Poland, Canada
A Study to Evaluate the Efficacy, Safety, and Tolerability of IMVT-1402 in Adult Participants With Active, Difficult to Treat Rheumatoid Arthritis
NCT06754462 · Rheumatoid Arthritis
Drug: IMVT-1402
Phase 2 Active, closed 2025-01 UK, USA, Germany, Spain, Poland, Czechia
Efficacy and Safety of IMVT-1402 in Adult Participants With Primary Sjogren's Disease With Moderate to Severe Systemic Disease Activity
NCT06979531 · Primary Sjögren's Syndrome
Drug: IMVT-1402
Phase 2 Active, closed 2025-06 UK, USA, Germany, Spain, Italy, Poland, Canada

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Immunovant Sciences in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with Immunovant Sciences as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A Randomized, Double-Blind, Placebo-Controlled, Phase 2b Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Patients With Graves' Disease
2025-521920-31-00 · CTIS ↗ · Immune System Diseases
Drug: IMVT-1402
Phase 2 Ongoing Italy, Poland, Greece + 6 more
03

Drugs in Immunovant Sciences trials

1 compound

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Immunovant Sciences trials

7 conditions
Graves' Disease3Chronic Inflammatory Demyelinating Polyneuropathy1Subacute Cutaneous Lupus Erythematosus1Chronic Cutaneous Lupus Erythematosus1Rheumatoid Arthritis1Generalized Myasthenia Gravis1Primary Sjögren's Syndrome1
06

Questions about Immunovant Sciences trials

How many clinical trials does Immunovant Sciences sponsor?

Immunovant Sciences is the lead sponsor of 8 current trials on ClinicalTrials.gov in our UK, USA, Poland, Spain, Germany, Italy, Czechia, Australia, Netherlands, Belgium, Denmark, Brazil, Mexico, Canada, South Korea, Israel, Ireland, Austria, Norway, Portugal, Turkey and Japan registers, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 12 November 2026. Completed and withdrawn studies are not counted.

Are Immunovant Sciences trials recruiting?

Yes. 4 of its 8 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Immunovant Sciences testing?

Its current trials name 1 drug or biological as interventions. The most frequent are IMVT-1402 (8). The number in brackets is how many of its trials name each drug.

Does Immunovant Sciences have clinical trials in Ireland?

Yes. 1 trial in our Ireland register (ClinicalTrials.gov). Some may be the same study registered in both. See the Irish clinical trials register for sites and contacts.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 12 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.