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

Study identifier:D9961C00001

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:2024-519015-34-00

Will Be Recruiting

Official Title

An Open-label, Phase I Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD5492 Following Single-ascending Dose and Step-up Dose Administration to Adult Participants with Systemic Lupus Erythematosus or Idiopathic Inflammatory Myopathies

Medical condition

Systemic Lupus Erythematosus

Phase

Phase 1

Healthy volunteers

Study drug

AZD5492

Sex

All

Estimated Enrollment

Study type

Interventional

Age

18 Years - 65 Years

Date

Study Start Date: 19 Mar 2025

Estimated Primary Completion Date: 25 Jan 2027

Estimated Study Completion Date: 25 Jan 2027

Study design

Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: -
Primary Purpose: Treatment

Verification:

Verified 01 Mar 2025 by AstraZeneca

Collaborators

Fortrea

Inclusion and 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:
(a) Diagnosis of SLE according to the 2019 EULAR/ACR classification criteria for SLE
(b) 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.
(c) Active, moderate-severe disease at screening, defined as clinical SLEDAI-2K ≥ 4.
(d) 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:
(a) 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.
(b) Positive for ≥ 1 disease-specific autoantibody performed by the central laboratory at screening.
(c) MMT-8 score of ≤ 142/150.
(d) 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:
(a) 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.
(b) 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:
(a) Active severe SLE-driven renal disease.
(b) 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.
(c) Rapidly progressive and/or severe ILD or ILD that requires oxygen supplementation/therapy (of any type).
(d) 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:
(a) FVC ≤60% of predicted
(b) DLCO ≤70% of predicted
(c) Deterioration in either FVC or DLCO at screening compared to pulmonary
function tests performed ≥3 months previously.
4 Infections
(a) Any clinical suspicion or diagnosis of active infection at screening.
(b) Opportunistic infection that meets criteria to be an SAE within 3 years.
(c) 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).
(d) 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.

Location

Research Site

Valladolid, Spain, 47012

Location

Research Site

Köln, Germany, 50937

Location

Research Site

Bunkyo-ku, Japan, 113-8655

Location

Research Site

Southampton, United Kingdom, SO16 6YD

Location

Research Site

Kitakyushu-shi, Japan, 807-8555

Location

Research Site

Sevilla, Spain, 41010

Location

Research Site

Anniston, AL, United States, 36207

Location

Research Site

London, United Kingdom, SE5 9RS

Arms	Assigned Interventions
Experimental: AZD5492 AZD5492 solution will be administered by subcutaneous injection either undiluted or diluted with 0.9% sodium chloride for injection	-

"There is no result for the study"

Documents available

Trial Results Summaries
Available here

Contacts

Contact

AstraZeneca Clinical Study Information Center

1-877-240-9479

information.center@astrazeneca.com

Sponsors

Collaborators

Inclusion Criteria

Exclusion Criteria

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Trial Results Summaries