A Study to Investigate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD5492 in Adult Participants With Systemic Lupus Erythematosus or Idiopathic Inflammatory Myopathies.

Study Purpose

The purpose of this study is to measure the safety, tolerability, PK, and PD of AZD5492 administered subcutaneously in adult participants with SLE or IIM. Study details include: • The study duration will be a minimum of 180 days in addition to the screening period. Additional follow-up visits may be required up to 12 months from study start.

  • - Depending on the study part they are assigned to, participants will be administered AZD5492 once (Part 1) or twice (Part 2).
  • - Study visits will occur at: Screening, Days 1-4, 8, 15, 22, 30, 60, 90, 120, 150, and 180 in Part 1, Screening, Days 1-4, 8-11, 15, 22, 29, 43, 60, 90, 120, 150, and 180 in Part 2.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years - 65 Years
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

1. Participant must be 18 to 65 years of age inclusive, at the time of signing the informed consent. 2. Diagnosis of SLE: 1. Diagnosis of SLE according to the 2019 EULAR/ACR classification criteria for SLE. 2. Positive for one or more of: anti-nuclear antibodies (titre ≥ 1:80), anti-dsDNA or anti-Sm performed by the central laboratory at screening. If anti-dsDNA or anti- Sm tests are negative, documented history of test results may be used. 3. Active, moderate-severe disease at screening, defined as clinical SLEDAI-2K ≥ 4. 4. Intolerance or inadequate response to ≥ 3 available treatments, used for at least 3 months each, such as the following: corticosteroids, anti-malarial drugs, calcineurin inhibitor, methotrexate, azathioprine, leflunomide, mycophenolic acid or its derivatives, cyclophosphamide, belimumab, anifrolumab, or B-cell depleting monoclonal antibodies. 3. Diagnosis of IIM: 1. Must have "probable" or "definite" diagnosis of PM or DM (excluding IBM and cancer associated myositis) according to the 2017 EULAR/ACR classification criteria for adult myositis. 2. Positive for ≥ 1 disease-specific autoantibody performed by the central laboratory at screening. 3. MMT-8 score of ≤ 142/150. 4. Fulfill at least one of the following criteria of active disease at screening: (i) One or more muscle enzyme elevation (CK, AST, ALT, aldolase, LDH) ≥ 1.3 × ULN (ii) If criterion 3(d)(i) is not met, then at least one of the following criteria must be met: a. Report from MRI performed within 3 months prior to screening with evidence of muscle inflammation b. Report from muscle biopsy performed within 3 months prior to screening that demonstrates active inflammation c. Report from electromyography performed within 3 months prior to screening that exhibits irritable myopathic pattern. (e) Intolerance or inadequate response to corticosteroids and ≥2 of the following treatments, used for at least 3 months each: calcineurin inhibitor, methotrexate, azathioprine, leflunomide, mycophenolic acid or its derivatives, cyclophosphamide, intravenous immunoglobulin (IVIG), or B-cell depleting monoclonal antibodies. 4. Must be receiving one of the following therapy regimens at screening: 1. Oral prednisolone (or equivalent) without additional immunosuppressive medication: Daily dose between 7.5 mg and 20 mg (inclusive) a day for ≥ 2 months prior to signing the ICF. Dose must be stable for ≥ 2 weeks prior to signing the ICF. 2. Immunosuppressive treatment with one of the following medications, at a stable dose for ≥ 3 months prior to signing the ICF: (i) Methotrexate ≤ 25 mg/week, without change of route of administration for 8 weeks prior to signing the ICF. (ii) Mycophenolate mofetil ≤ 2g/day (iii) Azathioprine ≤ 200 mg/day (iv) Leflunomide ≤ 15 mg/ day (v) Tacrolimus ≤ 0.1 mg/kg/day with maximum dose of 5 mg/day (vi) Cyclosporin ≤ 3 mg/kg/day with maximum dose of 200 mg/day. 5. Blood B-cells above 50 cells/μL at screening. 6. IgG levels > 6g/L at screening.

Exclusion Criteria:

1. Any complications of the disease under study which are judged by the investigator to be life or organ threatening or to require treatments which are not permitted in the protocol, including but not limited to: 1. Active severe SLE-driven renal disease. 2. History of, or current diagnosis of, catastrophic or severe APS (for example diagnosis of an arterial or central/pulmonary venous clot) within 1 year prior to signing the ICF. Participants with clinically evident APS which is adequately controlled by anticoagulants or aspirin for at least 12 weeks can be recruited into the study. 3. Rapidly progressive and/or severe ILD or ILD that requires oxygen supplementation/therapy (of any type). 4. Inclusion Body Myositis or cancer associated myositis. 2. Active severe, unstable or history of neuropsychiatric SLE including, but not limited to: aseptic meningitis; cerebral vasculitis; myelopathy; demyelination syndromes (ascending, transverse, acute inflammatory demyelinating polyradiculopathy); acute confusional state; impaired level of consciousness; psychosis; acute stroke or stroke syndrome; cranial neuropathy; status epilepticus; cerebral ataxia' and mononeuritis multiplex. 3. IIM: Pulmonary function tests at screening (or within one month of screening, provided participant confirms no change in respiratory symptoms in the interim) which meet any of the following criteria: 1. FVC ≤60% of predicted. 2. DLCO ≤70% of predicted. 3. Deterioration in either FVC or DLCO at screening compared to pulmonary function tests performed ≥3 months previously. 4 Infections. 1. Any clinical suspicion or diagnosis of active infection at screening. 2. Opportunistic infection that meets criteria to be an SAE within 3 years. 3. Clinically significant chronic infection (eg, osteomyelitis, bronchiectasis) with treatment completed less than 2 months prior to signing the ICF (except for chronic nail infections, which are allowed). 4. Any history of infection requiring: (i) Hospitalisation within the previous two months (ii) Treatment with IV anti-infectives with treatment completed less than 4 weeks prior to signing the ICF (iii) Oral anti-infectives within 2 weeks prior to signing the ICF. (e) History of recurrent infection requiring hospitalisation or IV antibiotics eg 3 or more of the same type of infection, including systemic fungal infections, over the previous 52 weeks. 5 Participants with HIV infection (confirmed by central laboratory at screening) 6 Participants with active EBV or CMV. 7 Participants with evidence of chronic or active hepatitis B defined as HBsAg positive or HBcAB positive 8 Participants with evidence of chronic or active hepatitis C defined as: (a) HCV IgM Ab positive (b) Detectable HCV RNA (c) Positive result for HCV IgG Ab is acceptable in the following circumstances: (i) HCV RNA is undetectable >12 weeks after completion of curative antiviral treatment for HCV. (ii) HCV RNA is undetectable on two occasions at least 12 weeks apart following resolution of HCV infection if not treated. 9 Participants with positive COVID-19 PCR. For participants with a positive COVID-19 reverse transcription PCR at screening, rescreening will be conducted not earlier than 6 weeks after the positive result. Only one rescreening is allowed. 10 Known history of a primary immunodeficiency, splenectomy, or any underlying condition that predisposes the participant to infection. 11 CNS pathology including but limited to the following: CNS vasculitis, severe brain injury, dementia, Parkinson's disease, neurodegenerative diseases, cerebellar disease, stroke, seizure disorder/epilepsy, PML, severe uncontrolled mental illness, psychosis, CNS involvement of autoimmune diseases. 12 Receipt of B-cell-depleting therapy including CD19 or CD20 directed monoclonal antibodies (including but not limited to, ocrelizumab, ofatumumab, obinutuzumab, or rituximab) <3 months prior to signing the ICF. If therapy was administered ≥3 months ago, exclude if absolute B-cell less than the lower limit of normal. 13 Prednisolone (or equivalent) > 20 mg within 2 months of signing the ICF.

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT06916806
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Phase 1
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

AstraZeneca
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

N/A
Principal Investigator Affiliation N/A
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Industry
Overall Status Recruiting
Countries Canada, China, France, Germany, Japan, Netherlands, Spain, United Kingdom, United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Systemic Lupus Erythematosus, Idiopathic Inflammatory Myopathies
Additional Details

This is an open-label, multi-centre Phase I study to assess the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of AZD5492 in adult participants with either SLE or IIM. Participants will be enrolled in approximately 20 sites in 8 countries. The study consists of 2 parts: Part 1

  • - Single ascending dose (SAD) Part 1 will be a sequential SAD design in adult participants with SLE.
Up to 5 dose levels of AZD5492 are planned to be investigated. Depending on emerging data, up to 4 additional dose levels may be added at the discretion of the Sponsor. The decision to open Part 2 will be made by the Safety Review Committee (SRC) based on the evaluation of all available data including safety, tolerability, PK, and PD from Part 1, and the dose levels and dosing strategy for Part 2 will be confirmed. After a screening period of up to 42 days, participants will receive 1 dose of AZD5492 and be followed up for at least 179 days post-dose. Part 2
  • - Step-up dosing (SUD) Part 2 will be a SUD design in adult participants with SLE, who previously did not participate in Part 1, and in adult participants with IIM.
In Part 2, participants will receive 2 dose administrations, where the second dose will be administered 7 days after the first dose. The first (priming) dose of the step-up regimen will be agreed by the SRC. The second (target) dose will be escalated, and a minimum of 3 target dose levels are planned to be investigated in Part 2.

Arms & Interventions

Arms

Experimental: Part 1: Single Ascending Dose with AZD5492

Participants will receive AZD5492 at an assigned dose as subcutaneous (SC) injection on Day 1.

Experimental: Part 2: Step-Up Dosing with AZD5492

Participants will receive AZD5492 as SC injection at the priming dose determined in Part 1, on Day 1, and at a target dose, based on the emergent safety data, on Day 8.

Interventions

Drug: - AZD5492

IMP: subcutaneous.

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Research Site, Anniston, Alabama

Status

Recruiting

Address

Research Site

Anniston, Alabama, 36207

International Sites

Research Site, Hamilton, Ontario, Canada

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Not yet recruiting

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Hamilton, Ontario, L8S 4K1

Research Site, Sherbrooke, Quebec, Canada

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Not yet recruiting

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Sherbrooke, Quebec, J1G 2E8

Research Site, Beijing, China

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Not yet recruiting

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Beijing, , 100730

Research Site, Shanghai, China

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Not yet recruiting

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Shanghai, , 200001

Research Site, Wuhan, China

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Not yet recruiting

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Wuhan, , 430022

Research Site, Bordeaux, France

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Not yet recruiting

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Bordeaux, , 33000

Research Site, Montpellier, France

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Not yet recruiting

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Montpellier, , 34295

Research Site, Nancy, France

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Not yet recruiting

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Nancy, , 54035

Research Site, Paris, France

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Not yet recruiting

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Paris, , 75013

Research Site, Strasbourg Cedex, France

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Not yet recruiting

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Strasbourg Cedex, , 67098

Research Site, Toulouse, France

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Not yet recruiting

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Toulouse, , 31059

Research Site, Erlangen, Germany

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Not yet recruiting

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Erlangen, , 91054

Research Site, Köln, Germany

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Not yet recruiting

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Köln, , 50937

Research Site, Magdeburg, Germany

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Not yet recruiting

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Magdeburg, , 39120

Research Site, Bunkyo-ku, Japan

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Not yet recruiting

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Bunkyo-ku, , 113-8655

Research Site, Kita-gun, Japan

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Not yet recruiting

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Research Site

Kita-gun, , 761-0793

Research Site, Kitakyushu-shi, Japan

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Not yet recruiting

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Kitakyushu-shi, , 807-8555

Research Site, Kyoto, Japan

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Not yet recruiting

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Kyoto, , 606-8501

Research Site, Nagasaki-shi, Japan

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Not yet recruiting

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Nagasaki-shi, , 852-8501

Research Site, Amsterdam, Netherlands

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Not yet recruiting

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Amsterdam, , 1105 AZ

Research Site, Leiden, Netherlands

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Not yet recruiting

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Leiden, , 2333

Research Site, Mérida, Spain

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Not yet recruiting

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Mérida, , 06800

Research Site, Sevilla, Spain

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Not yet recruiting

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Sevilla, , 41010

Research Site, Valladolid, Spain

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Not yet recruiting

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Valladolid, , 47012

Research Site, Glasgow, United Kingdom

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Not yet recruiting

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Glasgow, , G31 2ER

Research Site, London, United Kingdom

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Not yet recruiting

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London, , SE5 9RS

Research Site, London, United Kingdom

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Not yet recruiting

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London, , WC1E 6JF

Research Site, Southampton, United Kingdom

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Not yet recruiting

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Research Site

Southampton, , SO16 6YD