IgG4 Related DiseasePhase 3NCT04540497
A Study of Inebilizumab Efficacy and Safety in IgG4- Related Disease
A Phase 3 study testing Inebilizumab in people with IgG4 Related Disease, run by Amgen at 72 sites in 21 countries.
Trial summary
This study aims to evaluate the efficacy and safety of inebilizumab for the prevention of flare of Immunoglobulin G4-related disease (IgG4-RD). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- IgG4 Related Disease
- What is being tested?
- Inebilizumab
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 135 participants
- Where
- 72 sitesin 21 countries
- Study dates
- 4 Dec 2020to 31 Oct 2028
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male or female adults, ≥ 18 years of age at time of informed consent.
- Clinical diagnosis of IgG4-RD.
- Fulfillment of the 2019 ACR/EULAR classification criteria.
- Experiencing (or recently experienced) an IgG4-RD flare that requires initiation or continuation of glucocorticoid (GC) treatment at the time of informed consent.
- IgG4-RD affecting at least 2 organs/sites at any time in the course of IgG4-RD
- Non-sterilized male subjects who are sexually active with a female partner of childbearing potential must use a condom with spermicide from Day 1 through to the end of the study and must agree to continue using such precautions for at least 6 months after the final dose of IP. Females of childbearing potential who are sexually active with a non-sterilized male partner must use a highly effective method of contraception
Who cannot join
- History of solid organ or cell-based transplantation or known immunodeficiency disorder.
- Active malignancy or history of malignancy that was active within the last 10 years (some specific situations for cervical, skin or prostate cancer are acceptable).
- Receipt of any biologic B cell-depleting therapy or non-depleting B-cell-directed therapy in the 6 months prior to screening.
- Receipt of non-biologic DMARD or immunosuppressive agent other than GCs within 4 weeks prior to screening.
- Active tuberculosis or high risk for tuberculosis; hepatitis C infection in absence of curative treatment; evidence of hepatitis B infection.
- Receipt of live vaccine or live therapeutic infectious agent within 2 weeks prior to screening.
- Estimated glomerular filtration rate < 30 mL/min/1.73 m^2.
Trial locations and contacts
72 sites in 21 countries.
72 sites in 21 countries
China10 sites
Viela Bio Investigative Site 1
Beijing
Viela Bio Investigative Site 2
Beijing
Viela Bio Investigative Site 3
Beijing
Viela Bio Investigative Site 4
Beijing
Viela Bio Investigative Site 5
Beijing
Viela Bio Investigative Site
Guandong
Viela Bio Investigative Site
Hohhot, Inner Mongolia
Viela Bio Investigative Site
Shang’ai
Viela Bio Investigative Site
Shenyang
Viela Bio Investigative Site
Wuhan
Japan10 sites
Viela Bio Investigative Site
Fukuoka
Viela Bio Investigative Site
Hokkaido
Viela Bio Investigative Site
Hyōgo
Viela Bio Investigative Site
Ishikawa
Viela Bio Investigative Site
Kyoto
Viela Bio Investigative Site
Niigata
Viela Bio Investigative Site 2
Osaka
Viela Bio Investigative Site
Osaka
Viela Bio Investigative Site
Tokyo
Viela Bio Investigative Site
Toyama
Italy6 sites
Viela Bio Investigative Site
Florence
Viela Bio Investigative Site
Milan
Viela Bio Investigative Site
Pisa
Viela Bio Investigative Site
Reggio Emilia
Viela Bio Investigative Site
Torino
Viela Bio Investigative Site
Verona
France5 sites
Viela Bio Investigative Site
Clichy
Viela Bio Investigative Site
Lille
Viela Bio Investigative Site
Marseille
Viela Bio Investigative Site
Nantes
Viela Bio Investigative Site
Pessac
United States4 sites
Viela Bio Investigative Site
Atlanta, Georgia, 30322
Viela Bio Investigative Site
Baltimore, Maryland, 21287
Viela Bio Investigative Site
Boston, Massachusetts, 02114
Viela Bio Investigative Site
Palo Alto, California, 94305
Israel4 sites
Viela Bio Investigative Site
Kfar Saba
Viela Bio Investigative Site
Petah Tikva
Viela Bio Investigative Site
Tel Aviv
Viela Bio Investigative Site
Tel HaShomer
Spain4 sites
Viela Bio Investigative Site 2
Barcelona
Viela Bio Investigative Site
Barcelona
Viela Bio Investigative Site
Madrid
Viela Bio Investigative Site
Valencia
United Kingdom4 sites
Viela Bio Investigative Site
Leeds
Viela Bio Investigative Site
London
Viela Bio Investigative Site
Newcastle
Viela Bio Investigative Site
Oxford
Australia3 sites
Viela Bio Investigative Site
Adelaide, South Australia
Viela Bio Investigative Site
Auchenflower, Queensland
Viela Bio Investigative Site
Fitzroy
Canada3 sites
Viela Bio Investigative Site
Sherbrooke
Viela Bio Investigative Site 1
Toronto
Viela Bio Investigative Site 2
Toronto
Germany3 sites
Viela Bio Investigative Site
Berlin
Viela Bio Investigative Site
Lübeck
Viela Bio Investigative Site
München
Argentina2 sites
Viela Bio Investigative Site
Buenos Aires
Viela Bio Investigative Site
Mendoza
Hungary2 sites
Viela Bio Investigative Site
Debrecen
Viela Bio Investigative Site
Szeged
Netherlands2 sites
Viela Bio Investigative Site
Amsterdam
Viela Bio Investigative Site
Rotterdam
Poland2 sites
Viela Bio Investigative Site
Warsaw
Viela Bio Investigative Site
Wroclaw
Sweden2 sites
Viela Bio Investigative Site
Gothenburg
Viela Bio Investigative Site
Stockholm
Turkey (Türkiye)2 sites
Viela Bio Investigative Site
Ankara
Viela Bio Investigative Site
Istanbul
About this study
Official title: A Phase 3, Randomized, Double-blind, Multicenter, Placebo Controlled Study of Inebilizumab Efficacy and Safety in IgG4-Related Disease
This study aims to evaluate the efficacy and safety of inebilizumab for the prevention of flare of Immunoglobulin G4-related disease (IgG4-RD).
Read the detailed description
After a screening period of up to 28 days, subjects with IgG4-RD at high risk of flare due to multi-organ disease and recent active disease will be randomized in a 1:1 ratio to receive intravenous (IV) inebilizumab or placebo after premedication during the 52-week randomized control period (RCP). All subjects will receive an initial tapering dose of glucocorticoids (GCs) to complete treatment of their active disease. Flares occurring during study will be treated. The primary endpoint is time to a first adjudication committee-determined, investigator-treated disease flare during the RCP. The primary analysis will be conducted when the last subject completes the RCP visit or discontinues the RCP. This study includes an optional 3-year open-label treatment period. The study also includes a Safety Follow-up Period (SFUP) of up to 730 days for all participants. The expected duration of each subject's participation in this study is up to 400 days (screening and RCP), plus up to 1095 days for eligible subjects who enroll in the optional open label period (OLP), and up to 730 days for the SFUP, for a total maximum duration of up to 2273 days (screening, RCP, interval between RCP and OLP, OLP, and FSUP).
Study acquired from Horizon in 2024.
- Conditions
- IgG4 Related Disease
- Being tested
- Inebilizumab, Placebo
- Medical subject headings
- Immunoglobulin G4-Related Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
InebilizumabDrug
Inebilizumab is a monoclonal antibody that depletes B cells.
PlaceboOther
Placebo
| Study group | Role | What they receive |
|---|---|---|
| VIB0551 | Experimental | Inebilizumab administered as an IV infusion. Receives: Drug: Inebilizumab |
| Placebo | Placebo comparator | Placebo administered as an IV infusion. Receives: Other: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
RCP: Time to Disease Flare
Time to disease flare was defined as the number of days from Day 1 (dosing) to the date of the first treated and Adjudication Committee (AC)-determined IgG4-RD flare within the 52-week RCP. The date of disease flare was determined by the initiation of any flare treatment, including new or increased glucocorticoid (GC) treatment, other immunotherapy, or an interventional procedure, as deemed necessary by the Investigator to address the flare.
Kaplan-Meier (KM) method was used to estimate the median time to flare, and 95% confidence interval (CI).
Measured: Up to Week 52
Secondary outcomes (9)
RCP: Annualized Rate of Treated and AC-Determined Flares During the RCP
The annualized rate of treated and AC-determined flares during the 52-week RCP was calculated by dividing the total number of treated and AC-determined flares by the total time at risk (in years) for all participants. This measure reflected the frequency of disease flares per person per year during the RCP.
Measured: Week 52
RCP: Percentage of Participants Achieving Flare-free, Treatment-free Complete Remission at Week 52
Flare-free, treatment-free complete remission at Week 52 was defined as the absence of evident disease activity at Week 52, no AC-determined flare during the RCP, and no treatment for flare or disease control, except for the required 8-week glucocorticoid taper. Lack of evident disease activity was determined by either a score of 0 on the IgG4-RD Responder Index (score range: 0-4, with lower scores indicating better disease control) or an investigator's assessment that no disease activity was present based on physical, laboratory, pathology, or other evidence.
Measured: Week 52
RCP: Percentage of Participants Achieving Flare-free, Corticosteroid-free Complete Remission at Week 52
Flare-free, corticosteroid-free complete remission at Week 52 was defined as the absence of evident disease activity at Week 52, no AC-determined flare during the RCP, and no corticosteroid treatment for flare or disease control, except for the required 8-week glucocorticoid taper. Lack of evident disease activity was determined by either a score of 0 on the IgG4-RD Responder Index (score range: 0-4, with lower scores indicating better disease control) or an investigator's assessment that no disease activity was present based on physical, laboratory, pathology, or other evidence.
Measured: Week 52
Number of Participants Who Experienced Treatment-emergent Adverse Events (TEAEs) During the RCP
An adverse event (AE) referred to any untoward medical occurrence in a clinical study participant, regardless of a causal relationship with the study treatment. TEAEs included any event occurring after the participant received the study treatment. Clinically significant changes in vital signs, electrocardiograms, and laboratory tests recorded after treatment administration were documented as TEAEs. Serious AEs (SAEs) were untoward medical occurrences after the first dose, irrespective of a causal link to the study treatment, that led to death, were life-threatening, required hospitalization or its prolongation, caused significant disability, resulted in congenital anomalies, or were considered other medically important events. AEs were graded (Grade 3: severe; Grade 4: life-threatening; Grade 5: death) using the Common Terminology Criteria for Adverse Events [CTCAE]).
Measured: Up to Week 52
Number of Participants Who Experienced TEAEs During the OLP
An AE referred to any untoward medical occurrence in a clinical study participant, regardless of a causal relationship with the study treatment. TEAEs included any event occurring after the participant received the study treatment. Clinically significant changes in vital signs, electrocardiograms, and laboratory tests recorded after treatment administration were documented as TEAEs. SAEs were untoward medical occurrences after the first dose, irrespective of a causal link to the study treatment, that led to death, were life-threatening, required hospitalization or its prolongation, caused significant disability, resulted in congenital anomalies, or were considered other medically important events. AEs were graded (Grade 3: severe; Grade 4: life-threatening; Grade 5: death) using the CTCAE).
Measured: From the first dose of investigational product in OLP to the end of OLP or cutoff date; median (min, max) duration was 51.6 (0.1, 108.3) weeks.
RCP: Number of Participants With Anti-drug Antibodies (ADA) to Inebilizumab by Week 52
Incidence was the proportion of the participants with ADA positive post-baseline only or boosted their preexisting ADA (at least 4-fold over the baseline titer) during the study period. Baseline was defined as the last valid value on or before the first dose of RCP.
Measured: Baseline to Week 52
RCP: Time to Initiation of First Treatment for New or Worsening Disease Activity Within the RCP
Time to initiation of the first treatment (medication or procedure) for new or worsening disease activity, as determined by the investigator, within the RCP, was measured from day 1 (dosing) to the date the first treatment was administered. It Included any treatment initiated by the investigator for disease activity, regardless of the AC determination of flare.
KM method was used to estimate the median time to the initiation of first treatment or worsening of disease activity, and 95% CI.
Measured: Week 52
RCP: Annualized Flare Rate for AC-Determined IgG4-RD Flares at Week 52
The annualized flare rate for AC-determined IgG4-RD flares, whether or not treated, during the RCP was calculated by dividing the total number of AC-determined flares by the total time at risk (in years) for all participants. This measure reflected the frequency of IgG4-RD flares, irrespective of treatment, per participant per year during the study period.
Measured: Week 52
RCP: Cumulative Glucocorticoid (GC) Use for IgG4-RD Disease Control by Week 52
GC use was calculated as the cumulative glucocorticoid dose (in milligrams) taken for the purpose of IgG4-RD disease control during the RCP. This measure accounted for all GC treatments administered to participants to manage disease activity throughout the study period.
Measured: Week 52
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Sep 2020
- Study start4 Dec 2020
- Primary completion9 Apr 2024
- Study completion31 Oct 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for IgG4 Related DiseaseStudies of the same condition, open and under way.
- More trials run by AmgenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 135 participants (actual)
Sponsor and investigators
- Lead sponsor
- Amgen
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- MD, Study director, Amgen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04540497
- Sponsor's protocol ID
- VIB0551.P3.S2
- Other IDs
- 2023-508290-81-00, 2023
- Status last verified
- Nov 2025
- First submitted
- 1 Sep 2020
- Last updated
- 11 Dec 2025
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
- Expanded access
- Available
Publications
Tanaka Y, Umehara H, Sato H, Uchima K, Kouji K, Okazaki K. Inebilizumab treatment in Japanese patients with IgG4-related disease: a subgroup analysis of a randomized, double-blind, placebo-controlled, phase 3 trial (MITIGATE). Mod Rheumatol. 2026 Mar 6:roag020. doi: 10.1093/mr/roag020. Online ahead of print.
PubMed 41786624Stone JH, Khosroshahi A, Zhang W, Della Torre E, Okazaki K, Tanaka Y, Lohr JM, Schleinitz N, Dong L, Umehara H, Lanzillotta M, Wallace ZS, Ebbo M, Webster GJ, Martinez Valle F, Nayar MK, Perugino CA, Rebours V, Dong X, Wu Y, Li Q, Rampal N, Cimbora D, Culver EL; MITIGATE Trial Investigators. Inebilizumab for Treatment of IgG4-Related Disease. N Engl J Med. 2025 Mar 27;392(12):1168-1177. doi: 10.1056/NEJMoa2409712. Epub 2024 Nov 14.
PubMed 39541094Perugino C, Culver EL, Khosroshahi A, Zhang W, Della-Torre E, Okazaki K, Tanaka Y, Lohr M, Schleinitz N, Falloon J, She D, Cimbora D, Stone JH. Efficacy and Safety of Inebilizumab in IgG4-Related Disease: Protocol for a Randomized Controlled Trial. Rheumatol Ther. 2023 Dec;10(6):1795-1808. doi: 10.1007/s40744-023-00593-7. Epub 2023 Oct 4.
PubMed 37792260
Study at a glance
From the registry record, last updated by the sponsor on 11 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 3, Randomized, Double-blind, Multicenter, Placebo Controlled Study of Inebilizumab Efficacy and Safety in IgG4-Related Disease
- ClinicalTrials.gov ID
- NCT04540497
- Acronym / sponsor ID
- VIB0551.P3.S2
- Conditions
- IgG4 Related Disease
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 135 participants (actual)
- Lead sponsor
- AmgenIndustry (pharma, biotech, devices)
- Study start
- 4 Dec 2020 (actual)
- Primary completion
- 9 Apr 2024 (actual)
- Study completion
- 31 Oct 2028 (estimated)
- First posted
- 7 Sep 2020 (actual)
- Results
- Posted 25 Jun 2025
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims to evaluate the efficacy and safety of inebilizumab for the prevention of flare of Immunoglobulin G4-related disease (IgG4-RD).
Detailed description
After a screening period of up to 28 days, subjects with IgG4-RD at high risk of flare due to multi-organ disease and recent active disease will be randomized in a 1:1 ratio to receive intravenous (IV) inebilizumab or placebo after premedication during the 52-week randomized control period (RCP). All subjects will receive an initial tapering dose of glucocorticoids (GCs) to complete treatment of their active disease. Flares occurring during study will be treated. The primary endpoint is time to a first adjudication committee-determined, investigator-treated disease flare during the RCP. The primary analysis will be conducted when the last subject completes the RCP visit or discontinues the RCP. This study includes an optional 3-year open-label treatment period. The study also includes a Safety Follow-up Period (SFUP) of up to 730 days for all participants. The expected duration of each subject's participation in this study is up to 400 days (screening and RCP), plus up to 1095 days for eligible subjects who enroll in the optional open label period (OLP), and up to 730 days for the SFUP, for a total maximum duration of up to 2273 days (screening, RCP, interval between RCP and OLP, OLP, and FSUP).
Study acquired from Horizon in 2024.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| VIB0551 | Experimental | Drug: InebilizumabInebilizumab administered as an IV infusion. |
| Placebo | Placebo comparator | Other: PlaceboPlacebo administered as an IV infusion. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Male or female adults, ≥ 18 years of age at time of informed consent.
- Clinical diagnosis of IgG4-RD.
- Fulfillment of the 2019 ACR/EULAR classification criteria.
- Experiencing (or recently experienced) an IgG4-RD flare that requires initiation or continuation of glucocorticoid (GC) treatment at the time of informed consent.
- IgG4-RD affecting at least 2 organs/sites at any time in the course of IgG4-RD
Key exclusion criteria (7 listed)
- History of solid organ or cell-based transplantation or known immunodeficiency disorder.
- Active malignancy or history of malignancy that was active within the last 10 years (some specific situations for cervical, skin or prostate cancer are acceptable).
- Receipt of any biologic B cell-depleting therapy or non-depleting B-cell-directed therapy in the 6 months prior to screening.
- Receipt of non-biologic DMARD or immunosuppressive agent other than GCs within 4 weeks prior to screening.
- Active tuberculosis or high risk for tuberculosis; hepatitis C infection in absence of curative treatment; evidence of hepatitis B infection.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| InebilizumabInebilizumab is a monoclonal antibody that depletes B cells. | Drug | VIB0551 |
| PlaceboPlacebo | Other | Placebo |
Primary outcome
RCP: Time to Disease Flare
Time frame: Up to Week 52
Time to disease flare was defined as the number of days from Day 1 (dosing) to the date of the first treated and Adjudication Committee (AC)-determined IgG4-RD flare within the 52-week RCP. The date of disease flare was determined by the initiation of any flare treatment, including new or increased glucocorticoid (GC) treatment, other immunotherapy, or an interventional procedure, as deemed necessary by the Investigator to address the flare. Kaplan-Meier (KM) method was used to estimate the median time to flare, and 95% confidence interval (CI).
9 secondary outcomes
RCP: Annualized Rate of Treated and AC-Determined Flares During the RCP
Time frame: Week 52
RCP: Percentage of Participants Achieving Flare-free, Treatment-free Complete Remission at Week 52
Time frame: Week 52
RCP: Percentage of Participants Achieving Flare-free, Corticosteroid-free Complete Remission at Week 52
Time frame: Week 52
Number of Participants Who Experienced Treatment-emergent Adverse Events (TEAEs) During the RCP
Time frame: Up to Week 52
Number of Participants Who Experienced TEAEs During the OLP
Time frame: From the first dose of investigational product in OLP to the end of OLP or cutoff date; median (min, max) duration was 51.6 (0.1, 108.3) weeks.
RCP: Number of Participants With Anti-drug Antibodies (ADA) to Inebilizumab by Week 52
Time frame: Baseline to Week 52
RCP: Time to Initiation of First Treatment for New or Worsening Disease Activity Within the RCP
Time frame: Week 52
RCP: Annualized Flare Rate for AC-Determined IgG4-RD Flares at Week 52
Time frame: Week 52
RCP: Cumulative Glucocorticoid (GC) Use for IgG4-RD Disease Control by Week 52
Time frame: Week 52
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Dec 2025.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 41786624Tanaka Y, Umehara H, Sato H, Uchima K, Kouji K, Okazaki K. Inebilizumab treatment in Japanese patients with IgG4-related disease: a subgroup analysis of a randomized, double-blind, placebo-controlled, phase 3 trial (MITIGATE). Mod Rheumatol. 2026 Mar 6:roag020. doi: 10.1093/mr/roag020. Online ahead of print.
- Derived from this study: PubMed 39541094Stone JH, Khosroshahi A, Zhang W, Della Torre E, Okazaki K, Tanaka Y, Lohr JM, Schleinitz N, Dong L, Umehara H, Lanzillotta M, Wallace ZS, Ebbo M, Webster GJ, Martinez Valle F, Nayar MK, Perugino CA, Rebours V, Dong X, Wu Y, Li Q, Rampal N, Cimbora D, Culver EL; MITIGATE Trial Investigators. Inebilizumab for Treatment of IgG4-Related Disease. N Engl J Med. 2025 Mar 27;392(12):1168-1177. doi: 10.1056/NEJMoa2409712. Epub 2024 Nov 14.
- Derived from this study: PubMed 37792260Perugino C, Culver EL, Khosroshahi A, Zhang W, Della-Torre E, Okazaki K, Tanaka Y, Lohr M, Schleinitz N, Falloon J, She D, Cimbora D, Stone JH. Efficacy and Safety of Inebilizumab in IgG4-Related Disease: Protocol for a Randomized Controlled Trial. Rheumatol Ther. 2023 Dec;10(6):1795-1808. doi: 10.1007/s40744-023-00593-7. Epub 2023 Oct 4.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
MD study director
Amgen
72 sites in 21 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Inebilizumab in people with IgG4 Related Disease, run by Amgen at 72 sites in 21 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 11 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 72 sites in China, Japan, Italy, France, United States and 16 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 25 Jun 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
RCP: Time to Disease Flare (time frame: Up to Week 52). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04540497, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Dec 2025.