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AzTrials

Anti-N-methyl-D-aspartate Receptor (NMDAR) Encephalitis (ANRE)Phase 2NCT07093333

A Study in Participants With Anti-NMDAR Encephalitis and Anti-NMDAR Autoantibody-Associated Psychiatric Disease

A Phase 2 study testing ART5803 and ART5803-Cohort D in people with Anti-N-methyl-D-aspartate Receptor (NMDAR) Encephalitis (ANRE) and Anti-N-methyl-D-aspartate Receptor (NMDAR) Antibody-associated Psychiatric Disease, run by Arialys Australia Pty Ltd at 1 site in South Korea.

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Trial summary

This study will evaluate the safety, tolerability, preliminary efficacy and pharmacokinetics (PK) of ART5803 in adult participants with a confirmed diagnosis of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis (ANRE) or anti-NMDAR autoantibody-associated psychiatric disease Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
ART5803 and ART5803-Cohort D
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteSouth Korea
Study dates
15 May 2026to 30 May 2028
Phase
Phase 2
Are there results?
Not yet: the study is under way

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 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

7.3.1 Inclusion Criteria Individuals in Cohort A (participants with chronic ANRE) must meet all of the study inclusion criteria in Section 7.3.1.1. Individuals enrolled in Cohort B or Cohort C (participants with subacute or acute ANRE) must meet all of the study inclusion criteria in Section 7.3.1.2. Individuals in Cohort D (participants with anti-NMDAR autoantibody associated psychiatric disease) must meet all of the study inclusion criteria in Section 7.3.1.3.

Eligibility for participation in this study will be determined solely based on the participant meeting all protocol-defined inclusion and exclusion criteria. The legally authorized representative (LAR), where applicable, may provide informed consent on behalf of a participant who lacks the capacity to provide consent in accordance with local regulations; however, the LAR does not independently satisfy eligibility criteria. A participant who does not meet all required inclusion and exclusion criteria will not be enrolled in the study, regardless of the availability or status of an LAR.

7.3.1.1 Cohort A Inclusion Criteria The criteria below must be applied to all participants screened for Cohort A (participants with chronic ANRE) of the study.

Individuals eligible to participate in Cohort A must meet all the following criteria:

  1. The participant is a male or female who is of legal age to provide informed consent per local regulations, and ≤65 years of age at the time of informed consent. For the purposes of this study, the minimum age is 19 years in South Korea and 18 years in Australia.
  2. The participant, or their legally authorized representative (LAR), must be willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures. For participants who are unable to sign the consent form themselves, informed consent must be obtained from their LAR in accordance with local regulations and ethical guidelines.
  3. The participant, or their LAR, must ensure willingness and ability to comply with all study procedures to the extent possible, as determined by the Investigator.
  4. The participant has a diagnosis of ANRE according to the Graus et al criteria (Graus et al, 2016), with symptom onset >9 months to ≤36 months (or ≤120 months with Sponsor approval) prior to Week 0, Day 0.
  5. The participant has a positive cell-based assay result for CSF anti-NMDAR IgG autoantibody within 9 months of Week 0, Day 0. Participants without a positive CSF anti-NMDAR IgG autoantibody result within 9 months of Week 0, Day 0 may undergo a LP at Screening prior to the first study drug administration to confirm the presence of anti-NMDAR IgG autoantibodies in CSF (see Section 7.6.4.6.1). Note: If the participant has a documented history of positive anti-NMDAR IgG autoantibodies in CSF >9 months of Week 0, Day 0, they may be considered for inclusion in the study with confirmed positive anti-NMDAR IgG autoantibodies in serum at Screening at the discretion of the Investigator in collaboration with the Sponsor (see Section 7.6.4.6.1).
  6. Participants treated with IVIG must have completed treatment at least 7 days prior to Week 0, Day 0.
  7. Participants previously treated with immunotherapy must be receiving a stable dose (per Investigator discretion) for ≥1 month before Week 0, Day 0.
  8. Participants who are taking psychiatric medications (anti-depressants and antipsychotics) must remain on stable background psychiatric medications for at least 4 weeks prior to Week 0, Day 0 and for at least the first 6 weeks after Week 0, Day 0.
  9. Adequate disease burden as defined as any one of the following (a to c) at Screening and Week 0, Day 0:
  10. Two of the following: i. WAIS-IV immediate recall score <7 ii. TMT-A >40 seconds iii. RAVLT score <7 b. BDI-II total score ≥20. c. EQ 5D-5L score "moderate" or higher on at least 3 of the 5 items. Exceptions may be granted on a case-by-case basis in consultation with the Sponsor.
  11. No active malignancy (see Section 7.6.3.3) or residual teratoma. Prior teratoma must be fully resected ≥1 week before Week 0, Day 0 with no evidence of recurrence per work-up (imaging and tumor markers). Note: Discovery of a contralateral teratoma after study initiation will not be considered a protocol deviation. The event must be reported, managed per standard of care, and reviewed with the Sponsor Medical Monitor. Participants must have undergone appropriate cancer screening prior to study enrollment. The specific series of investigations used for each participant will occur according to the judgment of the treating Investigator (for example, MRI or CT of the chest, abdomen, and pelvis, and pelvic ultrasound for female participants) to exclude the presence or recurrence of an underlying neoplasm, such as ovarian teratoma or other malignancy. Documentation of imaging results must be available in the source documents.
  12. Sexually active female participants of childbearing potential and male participants with female partner(s) of childbearing potential must be willing to use a highly effective method of contraception during the study (from the time of providing consent) until at least 90 days after the last study drug administration, or longer if required by local regulations. In South Korea, contraception must be continued for 6 months after the last study drug administration in accordance with MFDS requirements. Examples of highly effective methods of contraception are provided in Appendix 1. The contraceptive methods used for male and female participants must be documented in the source documents.
  13. Female participants of childbearing potential must have a negative pregnancy test at Screening and be willing to have additional pregnancy tests during the study. Females considered not of childbearing potential include those who are surgically sterile (surgical bilateral oophorectomy, bilateral salpingectomy, or hysterectomy) confirmed by medical history or are post-menopausal (i.e., no menstrual bleeding for more than 2 years without an alternative medical cause and confirmation with more than 1 follicle stimulating hormone [FSH] measurement of at least >40 IU/L [or higher per local institutional guidelines]).Women of non-childbearing potential are not required to use any contraceptive method (see Appendix 1).
  14. Male participants must agree not to donate sperm, and female participants must agree not to donate eggs from the first study drug administration and until at least 90 days after the last dose of the study drug, or longer if required by local regulations. In South Korea, male participants must refrain from donating sperm for 6 months after the last study drug administration in accordance with MFDS requirements.
  15. Compliance with these restrictions must be documented at Screening and confirmed throughout the study.

7.3.1.2 Cohort B and Cohort C Inclusion Criteria The criteria below must be applied to all participants screened for Cohort B (participants with subacute ANRE) or Cohort C (participants with acute ANRE) of the study.

Individuals eligible to participate in Cohort B or C must meet all of the following criteria:

  1. The participant is a male or female who is of legal age to provide informed consent per local regulations, and ≤65 years of age at the time of informed consent. For the purposes of this study, the minimum age is 19 years in South Korea and 18 years in Australia.
  2. The participant, or their LAR, must be willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures. For participants who are unable to sign the consent form themselves, informed consent must be obtained from their LAR in accordance with local regulations and ethical guidelines.
  3. The participant, or their LAR, must ensure willingness and ability to comply with all study procedures to the extent possible, as determined by the Investigator.
  4. The participant has a diagnosis of ANRE according to the Graus et al criteria (Graus et al, 2016), with symptom onset ≥4 months and ≤9 months (Cohort B) or ≥0 months and <4 months (Cohort C) prior to Week 0, Day 0.
  5. Participants with ANRE symptoms as assessed by the mRS with a score of ≥3 during Screening and Week 0, Day 0.
  6. The participant has a positive cell-based assay result for CSF anti-NMDAR IgG autoantibody within 9 months for Cohort B and 4 months for Cohort C prior to Week 0, Day 0. Participants without a positive CSF anti-NMDAR IgG autoantibody result within 9 months for Cohort B and 4 months for Cohort C of Week 0, Day 0 may undergo a LP at Screening prior to the first study drug administration to confirm the presence of anti-NMDAR IgG autoantibodies in CSF (see Section 7.6.4.6.1). Note: If the participant documented history of positive anti-NMDAR IgG autoantibodies in CSF >9 months for Cohort B and >4 months for Cohort C, they may be considered for inclusion in the study with confirmed positive anti-NMDAR IgG autoantibodies in serum at Screening at the discretion of the Investigator in collaboration with the Sponsor (see Section 7.6.4.6.1).
  7. Participants treated with IVIG must have completed treatment at least 7 days prior to Week 0, Day 0.
  8. Immunotherapy:
  9. Cohort B: Participants previously treated with immunotherapy must be receiving a stable dose (per Investigator discretion) for ≥1 month before Week 0, Day 0.
  10. Cohort C: Participants may receive ART5803 regardless of previous or ongoing immunotherapy treatment status (per the Investigator's discretion).
  11. Participants who are taking psychiatric medications (anti-depressants and anti psychotics) must remain on stable background psychiatric medications for at least 4 weeks prior to Week 0, Day 0 and for at least the first 6 weeks after Week 0, Day 0.
  12. Participants treated with plasmapheresis must have completed treatment at least 1 day prior to Week 0, Day 0.
  13. Participants receiving steroids must be on a stable dose or a predefined taper regimen for at least 2 weeks prior to Week 0, Day 0.
  14. No active malignancy (see Section 7.6.3.3) or residual teratoma. Prior teratoma must be fully resected ≥1 week before Week 0, Day 0 with no evidence of recurrence per work-up (imaging and tumor markers). Note: Discovery of a contralateral teratoma after study initiation will not be considered a protocol deviation. The event must be reported, managed per standard of care, and reviewed with the Sponsor Medical Monitor.
  15. Participants must have undergone appropriate cancer screening prior to study enrollment. The specific series of investigations used for each participant will occur according to the judgment of the treating Investigator (for example, MRI or CT of the chest, abdomen, and pelvis, and pelvic ultrasound for female participants) to exclude the presence or recurrence of an underlying neoplasm, such as ovarian teratoma or other malignancy. Documentation of imaging results must be available in the source documents.
  16. Sexually active female participants of childbearing potential and male participants with female partner(s) of childbearing potential must be willing to use a highly effective method of contraception during the study (from the time of providing consent) until at least 90 days after the last study drug administration, or longer if required by local regulations. In South Korea, contraception must be continued for 6 months after the last study drug administration in accordance with MFDS requirements. Examples of highly effective methods of contraception are provided in Appendix 1. The contraceptive methods used for male and female participants must be documented in the source documents.
  17. Female participants of childbearing potential must have a negative pregnancy test at Screening and be willing to have additional pregnancy tests during the study. Females considered not of childbearing potential include those who are surgically sterile (surgical bilateral oophorectomy, bilateral salpingectomy, or hysterectomy) confirmed by medical history or are post-menopausal (i.e., no menstrual bleeding for more than 2 years without an alternative medical cause and confirmation with more than 1 FSH measurement of at least >40 IU/L [or higher per local institutional guidelines]).Women of non-childbearing potential are not required to use any contraceptive method (see Appendix 1).
  18. Male participants must agree not to donate sperm and female participants must agree not to donate eggs, from the first study drug administration and until at least 90 days after the last dose of the study drug, or longer if required by local regulations. In South Korea, male participants must refrain from donating sperm for 6 months after the last study drug administration in accordance with MFDS requirements.
  19. Compliance with these restrictions must be documented at Screening and confirmed throughout the study.

7.3.1.3 Cohort D Inclusion Criteria The criteria below must be applied to all participants screened for Cohort D (participants with anti-NMDAR autoantibody-associated psychiatric disease) of the study.

Individuals eligible to participate in Cohort D must meet all of the following criteria:

  1. The participant is a male or female who is of legal age to provide informed consent per local regulations, and ≤65 years of age at the time of informed consent. For the purposes of this study, the minimum age is 19 years in South Korea and 18 years in Australia.
  2. The participant, or their LAR, must be willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures. For participants who are unable to sign the consent form themselves, informed consent must be obtained from their LAR in accordance with local regulations and ethical guidelines.
  3. The participant, or their LAR, must ensure willingness and ability to comply with all study procedures to the extent possible, as determined by the Investigator.
  4. The participant has persistent psychotic symptoms for at least 2 months prior to Screening and Week 0, Day 0 as evaluated by the Investigator.
  5. The participant has marked deterioration of functioning in one or more areas, such as occupational, social, or personal care or hygiene.
  6. The participant has the documented presence of:
  7. Anti-NMDAR autoantibodies in CSF within 6 months of Week 0, Day 0; or
  8. Positive CSF anti-NMDAR autoantibody within 12 months of Week 0, Day 0 and positive serum anti-NMDAR autoantibody during Screening (see Section 7.6.4.6.1).
  9. Participants treated with IVIG must have completed treatment at least 7 days prior to Week 0, Day 0.
  10. Participants previously treated with immunotherapy must be receiving a stable dose (per Investigator discretion) for ≥1 month before Week 0, Day 0.
  11. Participants who are taking psychiatric medications (anti-depressants and anti psychotics) must remain on stable background psychiatric medications for at least 4 weeks prior to Week 0, Day 0 and for at least the first 6 weeks after Week 0, Day 0.
  12. Adequate disease burden as defined as both of the following:
  13. Participant must have a Positive and Negative Syndrome Scale (PANSS) total score ≥70 and a PANSS item score ≥4 (moderate) on 2 or more of the following PANSS items: delusions, conceptual disorganization, hallucinations, suspiciousness, and unusual thought content at Screening and Week 0, Day 0. Exceptions may be granted on a case-by-case basis in consultation with the Sponsor.
  14. Sexually active female participants of childbearing potential and male participants with female partner(s) of childbearing potential must be willing to use a highly effective method of contraception during the study (from the time of providing consent) until at least 90 days after the last study drug administration, or longer if required by local regulations. In South Korea, contraception must be continued for 6 months after the last study drug administration in accordance with MFDS requirements. Examples of highly effective methods of contraception are provided in Appendix 1. The contraceptive methods used for male and female participants must be documented in the source documents.
  15. Female participants of childbearing potential must have a negative pregnancy test at Screening and be willing to have additional pregnancy tests during the study. Females considered not of childbearing potential include those who are surgically sterile (surgical bilateral oophorectomy, bilateral salpingectomy, or hysterectomy) confirmed by medical history or are post-menopausal (i.e., no menstrual bleeding for more than 2 years without an alternative medical cause and confirmation with more than 1 FSH measurement of at least >40 IU/L [or higher per local institutional guidelines]).Women of non-childbearing potential are not required to use any contraceptive method (see Appendix 1).
  16. Male participants must agree not to donate sperm and female participants must agree not to donate eggs, from the first study drug administration and until at least 90 days after the last dose of the study drug, or longer if required by local regulations. In South Korea, male participants must refrain from donating sperm for 6 months after the last study drug administration in accordance with MFDS requirements.
  17. Compliance with these restrictions must be documented at Screening and confirmed throughout the study.

7.3.2 Exclusion Criteria Individuals (Cohorts A, B, C, or D) will not be eligible to participate in the study if they meet any of the exclusion criteria.

  1. The participant is pregnant or breastfeeding at Screening or planning to become pregnant (self or partner) at any time during the study.
  2. The participant has used an investigational product (IP) or investigational medical device within 30 days or 5 half-lives of the other IP (whichever is longer) prior to Screening or is required to use any investigational agent prior to completion of all scheduled study assessments.
  3. The participant has used an NMDAR modulator other than the study drug (e.g., ketamine, memantine, dextromethorphan, amantadine, ifenprodil, phencyclidine, acamprosate, D-cycloserine) from within 5 half-lives of the NMDAR modulator prior to Week 0, Day 0.
  4. The participant has previous exposure to ART5803 or other antibody that targets NMDAR.
  5. Participant has any condition that, in the opinion of the Investigator, would interfere with the evaluation or administration of the IP, interpretation of participant safety or study results, or would make participation in the study an unacceptable risk.
  6. Participant with coexisting CNS demyelinating disorders (e.g., multiple sclerosis), known positivity to other autoantibodies associated with autoimmune encephalitis, or any significant history of a psychiatric or neurologic disorder other than ANRE should undergo consultation with the Sponsor Medical Monitor on a case-by-case basis for eligibility determination. MOG antibody positivity may be permitted on a case-by-case basis if the condition is clinically inactive and not expected to confound study assessments.
  7. The participant has a confirmed positive test for hepatitis B serology (hepatitis B surface antigen and core antigen) and/or hepatitis C polymerase chain reaction at Screening.
  8. The participant has a known history of allergy or reaction to any component of the investigational agent (ART5803), or history of anaphylaxis following any biologic therapy.
  9. The participant has a history (within 12 months prior to Screening for Cohorts A, B, or C) or current (for Cohort D) alcohol abuse or drug addiction, defined as moderate or severe substance use disorder per Diagnostic and Statistical Manual for Mental Disorders, Fifth Edition, or any pattern of alcohol or substance use that, in the Investigator's judgment and after discussion with the

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

South Korea1 site, 1 recruiting
  • Seoul National University Hospital

    Seoul, 03080

    Soon-Tae Lee, MD, +82-2-2072-4757, staelee@snu.ac.kr

    Recruiting

Other trials in South Korea

About this study

Official title: A Phase 2a, Open-label Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of ART5803 in Participants With Anti-NMDAR Encephalitis and AntiNMDAR Autoantibody-Associated Psychiatric Disease

This study will evaluate the safety, tolerability, preliminary efficacy and pharmacokinetics (PK) of ART5803 in adult participants with a confirmed diagnosis of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis (ANRE) or anti-NMDAR autoantibody-associated psychiatric disease

Read the detailed description

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is one of the most common causes of autoimmune encephalitis. The disease is caused by the development of autoantibodies against the amino (N)-terminal domain (NTD) of the NMDAR subunit 1 (NR1) that bind and cross link the receptors, leading to receptor internalization and loss of function.

Arialys has developed a monovalent (one-armed) antibody, ART5803, that binds to the NTD of the NMDAR NR1 subunit without causing NMDAR inhibition, activation, or receptor internalization, while simultaneously blocking the ability of the pathogenic anti-NMDAR autoantibodies to bind to the receptor. There is also an increasing body of data supporting the potential link between broader psychiatric diseases and the presence of autoantibodies against the NMDAR.

Being tested
ART5803, ART5803-Cohort D
Keywords
Anti-N-methyl-D-aspartate receptor (NMDAR), Encephalitis, Anti-N-methyl-D-aspartate receptor (NMDAR) Encephalitis
Medical subject headings
Encephalitis, Autoimmune Diseases of the Nervous System

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ART5803Drug

    A monovalent (one-armed) antibody, that binds to the NTD of the NMDAR NR1 subunit without causing NMDAR inhibition, activation, or receptor internalization, while simultaneously blocking the ability of the pathogenic anti-NMDAR autoantibodies to bind to the receptor.

    1. Sentinel participants: 30 mg/kg
    2. Subsequent participants: up to 60 mg/kg
    3. Schedule: Q1W for 4 doses then Q2W for 4 doses
  • ART5803-Cohort DDrug

    A monovalent (one-armed) antibody, that binds to the NTD of the NMDAR NR1 subunit without causing NMDAR inhibition, activation, or receptor internalization, while simultaneously blocking the ability of the pathogenic anti-NMDAR autoantibodies to bind to the receptor.

    Participants receive ART5803 by intravenous infusion once a week for 4 weeks, then every 2 weeks for 8 weeks, for a total of 8 doses. Sentinel participants receive 30 mg per kg. Additional participants may receive up to 60 mg per kg based on Safety Review Committee guidance.

Study groups in NCT07093333
Study groupRoleWhat they receive
Cohort A: Adult patients with chronic ANREExperimentalNot described
Receives: Drug: ART5803
Cohort B: Adult patients with subacute ANREExperimentalNot described
Receives: Drug: ART5803
Cohort C: Adult patients with acute ANREExperimentalNot described
Receives: Drug: ART5803
Cohort D: Adult patients with anti-NMDAR autoantibody-associated psychiatric diseaseExperimentalNot described
Receives: Drug: ART5803-Cohort D

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To assess the safety and tolerability of ART5803

    Incidence and severity of Treatment-Emergent Adverse Events (TEAEs)

    Measured: 26 weeks

  2. To assess the safety and tolerability of ART5803

    Clinically significant changes in physical examination findings.

    Measured: 26 weeks

  3. To assess the safety and tolerability of ART5803

    Clinically significant changes in neurological examination findings

    Measured: 26 weeks

  4. To assess the safety and tolerability of ART5803

    Vital signs - Systolic and diastolic blood pressure

    Measured: 26 weeks

  5. To assess the safety and tolerability of ART5803

    Vital signs- Pulse rate

    Measured: 26 weeks

  6. To assess the safety and tolerability of ART5803

    Vital signs- Body temperature

    Measured: 26 weeks

  7. To assess the safety and tolerability of ART5803

    Vital signs- Respiratory rate

    Measured: 26 weeks

  8. To assess the safety and tolerability of ART5803

    Clinical laboratory outcomes - Serum anti-ART5803 binding antibodies (ADA)

    Measured: 26 weeks

  9. To assess the safety and tolerability of ART5803

    Concomitant medications

    Measured: 26 weeks

  10. To assess the safety and tolerability of ART5803

    Change in suicidal tendency as measured by the incidence of positive responses (Yes) to Item 4 or 5 on the Columbia-Suicide Severity Rating Scale (C-SSRS) from baseline (Score range: 0-5 per item. Higher score indicated better symptoms)

    Measured: 26 weeks

  11. To assess the safety and tolerability of ART5803

    Presence of anti-drug antibodies (ADAs)

    Measured: 26 weeks

  12. To assess the safety and tolerability of ART5803

    Clinical laboratory outcomes - Hematology

    Measured: 26 weeks

  13. To assess the safety and tolerability of ART5803

    Clinical laboratory outcomes - Serum Chemistry

    Measured: 26 weeks

  14. To assess the safety and tolerability of ART5803

    12-lead Electrocardiogram (ECG) findings - QRS interval >120 ms

    Measured: 26 weeks

Secondary outcomes (35)
  1. To assess the effects of ART5803 on Patient Reported Outcomes (PROs)

    Change from baseline in patient reported endpoints: Short Form Health Survey, Version 2 (SF-36-II) mental component domain score (Score range: 0-100. Higher score indicated better symptoms) (Cohort A only)

    Measured: 26 weeks

  2. To assess the effects of ART5803 on Patient Reported Outcomes (PROs)

    Change from baseline in patient reported endpoints: Trail Making Test, Part A (TMT-A) scores (Time to complete (higher = worse)) (Cohort A only)

    Measured: 26 weeks

  3. To assess the effects of ART5803 on Patient Reported Outcomes (PROs)

    Change from baseline in patient reported endpoints: European Quality of Life, 5-dimension, 5-level (EQ-5D-5L) scores (Score range: -0.281 to 1. Higher score indicated better symptoms) (Cohort A only)

    Measured: 26 weeks

  4. To assess the effects of ART5803 on Patient Reported Outcomes (PROs)

    Change from baseline in patient reported endpoints: Beck Depression Inventory-II (BDI-II) scores (Score range: 0-63. Higher score indicated worse symptoms) (Cohort A only)

    Measured: 26 weeks

  5. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints: Wechsler Adult Intelligence Scale, Fourth Edition (WAIS-IV) Digit Span (Score varies) (Cohort A only)

    Measured: 26 weeks

  6. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints: Rey Auditory Verbal Learning Test (RAVLT) immediate recall 1 to 5 and delayed recall (Cohort A only)

    Measured: 26 weeks

  7. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints: Rey-Osterrieth Complex Figure Test (36-point scoring) (ROCF-36) delayed recall component score (Score range: 0-36. Higher score indicated better symptoms) (Cohort A only)

    Measured: 26 weeks

  8. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints: Brief Social Aptitude Test (BSAT) number of errors (Cohort A only)

    Measured: 26 weeks

  9. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints: Boston Naming Test score (Score range: 0-60. Higher score indicated better symptoms) (Cohort A only)

    Measured: 26 weeks

  10. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints: Verbal Fluency Test score (Score varies) (Cohort A only)

    Measured: 13 weeks

  11. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints at Weeks 5 and 11:

    Positive and Negative Syndrome Scale (PANSS) score (Score range: 30-210. Higher score indicated worse symptoms)

    Measured: 26 weeks

  12. To assess the changes in neurological and behavioral outcomes following ART5803 administration

    Change from baseline in Clinical Assessment Scale for Autoimmune Encephalitis (CASE) outcomes (Score range: 0-27. Higher score indicated worse symptoms)

    Measured: 11 weeks

  13. To assess the changes in neurological and behavioral outcomes following ART5803 administration

    Change from baseline in Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) score (Score range: 40-160. Higher score indicated better symptoms)

    Measured: 26 weeks

  14. To assess changes in mobility and disability in basic and instrumental activities in daily living outcomes following ART5803 administration

    In absence of rescue therapy:

    Proportion of participants with ≥1 point improvement in mRS from baseline to Week 11 Change from baseline in mRS score at Week 1, 3, 7, 11, 16, 20, 26 and ET/EOS as determined by rank analyses, integrating need for rescue therapy and time to achievement of the mRS Time to mRS improvement from baseline by ≥1 point (Speed of Recovery) Time to mRS ≤2

    Measured: 26 weeks

  15. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints at Weeks 5 and 11:

    Scale for the Assessment of Negative Symptoms (SANS) score (Score range: 0-125. Higher score indicated worse symptoms) (Cohort D only)

    Measured: 26 weeks

  16. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints at Weeks 5 and 11: Clinical Global Impression-Severity (CGI-S) score (Score range: 1-7. Higher score indicated worse symptoms)

    Measured: 26 weeks

  17. To assess the effects of ART5803 on neuropsychological assessments

    Change from baseline in neuropsychological endpoints at Weeks 5 and 11:

    Change in neuropsychological endpoint Clinical Global Impression-Improvement (CGI-I) score (Score range: 1-7. Higher score indicated worse symptoms)

    Measured: 26 weeks

  18. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by maximum concentration (Cmax)

    Measured: 26 weeks

  19. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by last time point with measurable concentration (Clast)

    Measured: 26 weeks

  20. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by by last time point with minimum concentration (Cmin)

    Measured: 26 weeks

  21. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by time at which Cmax is observed (tmax)

    Measured: 26 weeks

  22. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by area under the curve from time 0 to the last measurable concentration (AUC0-t)

    Measured: 26 weeks

  23. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by area under the curve from time 0 extrapolated to infinity (AUC0-∞)

    Measured: 26 weeks

  24. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by the half-life (t½)

    Measured: 26 weeks

  25. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by the volume of distribution (Vd)

    Measured: 26 weeks

  26. Serum PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by clearance (CL)

    Measured: 26 weeks

  27. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by maximum concentration (Cmax)

    Measured: 12 weeks

  28. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by last time point with measurable concentration (Clast)

    Measured: 12 weeks

  29. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by by last time point with minimum concentration (Cmin)

    Measured: 12 weeks

  30. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by time at which Cmax is observed (tmax)

    Measured: 12 weeks

  31. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by area under the curve from time 0 to the last measurable concentration (AUC0-t)

    Measured: 12 weeks

  32. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by area under the curve from time 0 extrapolated to infinity (AUC0-∞)

    Measured: 12 weeks

  33. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by the half-life (t½)

    Measured: 12 weeks

  34. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by the volume of distribution (Vd)

    Measured: 12 weeks

  35. Cerebrospinal Fluid (CSF) PK parameters of ART5803

    To characterize and compare the PK profile of ART5803 as measured by clearance (CL)

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Jul 2025
  2. Study start15 May 2026
  3. Primary completion30 Nov 2027 (estimated)
  4. Study completion30 May 2028 (estimated)

Resources

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 2
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07093333
Sponsor's protocol ID
ART5803-201
Status last verified
Oct 2026
First submitted
19 Jun 2025
Last updated
27 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing ART5803 and ART5803-Cohort D in people with Anti-N-methyl-D-aspartate Receptor (NMDAR) Encephalitis (ANRE) and Anti-N-methyl-D-aspartate Receptor (NMDAR) Antibody-associated Psychiatric Disease, run by Arialys Australia Pty Ltd at 1 site in South Korea.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

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: looking for participants now, as of the sponsor's last update on 27 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Korea. 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. 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact April Purcell (1-619-865-6365, apurcell@arialysrx.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To assess the safety and tolerability of ART5803 (time frame: 26 weeks). The study lists 14 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 27 Oct 2026.

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