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A Study of GKL-006Allo Injection in Patients With Ankylosing Spondylitis

2026. október 30. frissítette: Beijing Gene Key Life Technology Co., Ltd

A Phase 1 Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Preliminary Efficacy of GKL-006Allo Injection in Patients With Ankylosing Spondylitis

Ankylosing spondylitis (AS) is a long-term inflammatory disease that mainly affects the spine and sacroiliac joints, causing back pain and stiffness. Some patients do not respond well to existing treatments. This study will test an investigational cell therapy called GKL-006Allo injection, made from donor-derived invariant natural killer T (iNKT) cells and given by intravenous infusion.

The study will evaluate two dose levels of GKL-006Allo, given once every two weeks for up to 11 doses. The study starts at a lower dose. After a safety review committee confirms the safety of the current dose level, the study may move to a higher dose. The main purposes are to find out how safe and well tolerated GKL-006Allo is, how it moves through the body (pharmacokinetics), whether it triggers an immune response (immunogenicity), and to collect early information on whether it improves AS.

Researchers will monitor participants for 52 weeks after the first dose to track safety and disease-related measures.

A tanulmány áttekintése

Állapot

Még nincs toborzás

Körülmények

Beavatkozás / kezelés

Tanulmány típusa

Beavatkozó

Beiratkozás (Becsült)

12

Fázis

  • 1. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi kapcsolat

Tanulmányi helyek

      • Beijing, Kína
        • First Medical Center of Chinese PLA General Hospital
        • Kapcsolatba lépni:

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

18 év (Felnőtt, Idősebb felnőtt)

Egészséges önkénteseket fogad

Nem

Tanulmányozható nemek

Összes

Leírás

Inclusion Criteria:

  1. Participants must be able to understand the informed consent form and voluntarily agree to participate, with a signed and dated informed consent form.
  2. Age 18 to 65 years (inclusive), both sexes.
  3. Diagnosis of ankylosing spondylitis (AS) according to the 1984 modified New York criteria, and classification as axial spondyloarthritis (axSpA) according to the 2025 ASAS-SPARTAN axSpA classification criteria. Participants must have active disease, meeting both of the following criteria: (a) Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) score >= 4; and (b) spinal pain score >= 4 as measured by BASDAI question 2.
  4. Prior treatment with at least 2 nonsteroidal anti-inflammatory drugs (NSAIDs) at full dose on a regular schedule for at least 4 weeks, with no significant improvement in symptoms as assessed by the investigator; or intolerance to NSAIDs (discontinuation of NSAID treatment due to treatment-related adverse events, such as allergic reactions or gastrointestinal signs or symptoms; the 4-week treatment duration requirement does not apply in this case); or contraindication to NSAID treatment.
  5. Participants who have received no more than 1 prior biologic agent or JAK inhibitor (agents with the same generic name count as 1): treatment must have been administered at the recommended dose for at least 12 weeks with inadequate response, intolerance (adverse events leading to discontinuation), or inability to continue for other reasons. Washout periods before the first dose: etanercept, 4 weeks; infliximab, 8 weeks; adalimumab, certolizumab pegol, or golimumab, 10 weeks; IL-17 inhibitors, 12 weeks; JAK inhibitors, 4 weeks; biologic classes not listed, 5 drug half-lives.
  6. If participants are receiving methotrexate (MTX), sulfasalazine (SSZ), or hydroxychloroquine (HCQ), the treatment duration before enrollment must be at least 3 months, and the dose must have been stable for at least 4 weeks.
  7. Participants of childbearing potential must use at least 1 medically accepted contraceptive method during the study treatment period and for 6 months after the end of study treatment. Serum human chorionic gonadotropin (HCG) must be negative within 7 days before the first dose for women of childbearing potential; participants must be non-lactating and non-pregnant.
  8. Able to communicate well with the investigator and comply with the requirements of the study.

Exclusion Criteria:

  1. Allergy to immunotherapy or to the excipients of the investigational drug.
  2. Known or suspected history of complete spinal ankylosis, or complete spinal ankylosis confirmed clinically and radiographically.
  3. Complete ankylosis of the sacroiliac joints.
  4. Spinal or joint surgery within 2 months before dosing, or planned spinal or joint surgery during the study period.
  5. Other untreated malignancy within the past 5 years or concomitant malignancy, except adequately treated skin basal cell carcinoma, carcinoma in situ, and breast cancer with no recurrence for more than 3 years after curative surgery.
  6. Any active, known, or suspected autoimmune disease other than the indication under study (including but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, vasculitis, glomerulonephritis, uveitis, hypophysitis, and hyperthyroidism). Exceptions: type 1 diabetes mellitus on stable-dose insulin therapy for at least 3 months before enrollment; hypothyroidism requiring only hormone replacement therapy; and skin conditions (such as eczema, vitiligo, or psoriasis) requiring no systemic treatment and without acute exacerbation within 1 year before screening.
  7. Severe trauma or major surgery (such as transabdominal or transthoracic surgery) within 6 months before screening, or planned major surgery during the study.
  8. History of idiopathic pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, radiation pneumonitis (may be enrolled if only detected on imaging and no corticosteroid treatment is required), or drug-induced pneumonitis.
  9. Poorly controlled cardiac signs, symptoms, or diseases: (a) congestive heart failure of NYHA class II or above; Poorly controlled cardiac signs, symptoms, or diseases: (a) heart failure of New York Heart Association (NYHA) class II or above;b) unstable angina within 6 months; (c) acute myocardial infarction within 1 year; (d) clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention (such as QTc > 450 msec in males or > 470 msec in females).
  10. Hypertension not well controlled by antihypertensive medication (systolic blood pressure >= 140 mmHg or diastolic blood pressure >= 90 mmHg within 7 days before enrollment).
  11. Cerebrovascular or cardiovascular events within 3 months before dosing (myocardial infarction, ischemic or hemorrhagic stroke excluding lacunar infarction, deep vein thrombosis, etc.).
  12. Any of the following at screening or baseline: (a) aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 2.5 x ULN; (b) serum creatinine > 1.5 x ULN or glomerular filtration rate < 60 mL/min/1.73 m2; (c) activated partial thromboplastin time (APTT) > 1.5 x ULN or prothrombin time (PT) > 2.5 x ULN (without anticoagulant therapy); (d) left ventricular ejection fraction <= 50%; (e) urine protein > 2+ on urinalysis within 7 days before enrollment, confirmed by 24-hour urine protein quantification > 1.0 g; (f) white blood cell count < 3 x 10^9/L, hemoglobin < 90 g/L, absolute neutrophil count < 1.5 x 10^9/L, or platelet count < 90 x 10^9/L.
  13. Any of the following bleeding conditions: bleeding events of CTCAE v6.0 grade 2 or above within 4 weeks before enrollment; gastrointestinal bleeding history or definite gastrointestinal bleeding within 6 months before enrollment, or bleeding from esophageal and/or gastric varices without endoscopic or transjugular intrahepatic portosystemic shunt prophylaxis; known hereditary or acquired bleeding or thrombotic tendency (such as hemophilia or coagulation disorders).
  14. Systemic active infection requiring treatment within 2 weeks before enrollment, or unexplained fever with temperature >= 38.5 degrees C within 7 days before enrollment.
  15. Congenital or acquired immunodeficiency (such as HIV infection); active syphilis infection; positive tuberculosis test.
  16. HBV or HCV infection at screening with viral load above the lower limit of detection (HBV DNA >= 10 IU/mL or HCV RNA >= 10 IU/mL).
  17. Prior receipt of genetically modified cell therapy, or receipt of non-genetically modified cell therapy within 6 months before screening.
  18. Prior use of oral glucocorticoids, or receipt of glucocorticoids by any intra-articular, intramuscular, or intravenous injection.
  19. Receipt of disease-modifying antirheumatic drugs (DMARDs) other than sulfasalazine and hydroxychloroquine within 1 month before dosing; leflunomide discontinued for less than 8 weeks; or discontinuation for less than 5 drug half-lives according to the actual drug class (i.e., the DMARD washout period should exceed 5 half-lives of the corresponding drug), whichever is longer.
  20. Current use of strong opioid analgesics (such as methadone, hydromorphone, or morphine).
  21. Vaccination with live or attenuated vaccines within 4 weeks before screening.
  22. Enrollment in another clinical study of a drug or device within 4 weeks before screening.
  23. Other factors judged by the investigator that may lead to premature study termination, such as other serious concomitant diseases (including severe diabetes, thyroid disease, spinal cord compression, superior vena cava syndrome, or psychiatric illness), severe laboratory abnormalities, or family or social factors that may affect participant safety or the collection of data and samples.
  24. Intolerance to venipuncture, or history of needle or blood phobia.
  25. History of alcoholism, drug abuse, or use of any illicit drugs.
  26. Other factors considered by the investigator to be unsuitable for enrollment or likely to affect participant participation or completion of the study.

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Kezelés
  • Kiosztás: N/A
  • Beavatkozó modell: Egyetlen csoportos hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Kísérleti: GKL-006Allo Injection

Participants receive GKL-006Allo injection by intravenous infusion once every two weeks for up to 11 doses. Participants are assigned to one of two dose levels, a low dose of (3.0±0.9)×10^8 cells/m2 or a high dose of (9.0±2.7)×10^8 cells/m2, with the low-dose level enrolled first and the high-dose level opened after safety review per the dose-escalation rules.

Allogeneic invariant natural killer T (iNKT) cells administered by intravenous infusion once every two weeks for up to 11 doses. Dose escalation from (3.0±0.9)×10^8 cells/m2 to (9.0±2.7)×10^8 cells/m2 per the 3+3 dose-escalation design.

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Dose-limiting toxicities (DLTs) of GKL-006Allo injection
Időkeret: 28 days after the first dose of GKL-006Allo

Number and percentage of participants experiencing DLTs at each dose level during the DLT observation window, assessed per protocol-defined criteria.

28 days after the first dose of GKL-006Allo
Frequency of adverse events (AEs) and serious adverse events (SAEs)
Időkeret: From first dose through end of study (approximately 52 weeks after first dose)

Number and percentage of participants with AEs and SAEs, including treatment-emergent events, graded according to the Common Terminology Criteria for Adverse Events (CTCAE) v6.0.

From first dose through end of study (approximately 52 weeks after first dose)
Change from baseline in systolic blood pressure
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

Vital signs will be measured at each scheduled visit. Descriptive statistics will be provided for observed values and changes from baseline.Units: mmHg.

Baseline through end of study (approximately 52 weeks after first dose)
Change from baseline in diastolic blood pressure
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

Vital signs will be measured at each scheduled visit. Descriptive statistics will be provided for observed values and changes from baseline.Units: mmHg.

Baseline through end of study (approximately 52 weeks after first dose)
Change from baseline in pulse rate
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

Vital signs will be measured at each scheduled visit. Descriptive statistics will be provided for observed values and changes from baseline.Units: beats per minute (bpm).

Baseline through end of study (approximately 52 weeks after first dose)
Change from baseline in respiratory rate
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

Vital signs will be measured at each scheduled visit. Descriptive statistics will be provided for observed values and changes from baseline.Units: beats per minute (bpm).

Baseline through end of study (approximately 52 weeks after first dose)
Change from baseline in body temperature
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

Vital signs will be measured at each scheduled visit. Descriptive statistics will be provided for observed values and changes from baseline.Units:degrees Celsius (°C).

Baseline through end of study (approximately 52 weeks after first dose)
Number of participants with clinically significant changes from baseline in physical examination findings
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

Physical examinations will be performed at each scheduled visit. Post-dose findings will be graded by the most severe clinical significance assessment recorded after dosing. The number of participants with abnormal findings at baseline without clinical significance that became abnormal with clinical significance after dosing will be summarized.

Baseline through end of study (approximately 52 weeks after first dose)
Number of participants with clinically significant shifts from baseline in laboratory test results
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

Laboratory tests include hematology, serum chemistry, coagulation, urinalysis, and thyroid function tests. Cross-tabulations of baseline and post-baseline results (by clinical significance) will be provided. The number of participants shifting from normal at baseline to abnormal after dosing, and from abnormal without clinical significance at baseline to abnormal with clinical significance after dosing, will be summarized by test category.

Baseline through end of study (approximately 52 weeks after first dose)
Number of participants with abnormal 12-lead electrocardiogram (ECG) findings
Időkeret: Baseline through end of study (approximately 52 weeks after first dose)

12-lead ECGs (including heart rate, rhythm, and RR, PR, QRS, and QTc intervals) will be recorded at each scheduled visit and assessed for clinical significance. Participants with normal baseline ECG becoming abnormal after dosing, and participants with abnormal baseline ECG without clinical significance becoming abnormal with clinical significance after dosing, will be counted.

Baseline through end of study (approximately 52 weeks after first dose)

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Assessment of SpondyloArthritis International Society (ASAS)20 response rate
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Proportion of participants achieving an ASAS20 response. ASAS20 response is defined as at least 20% improvement from baseline in at least 3 of the 4 ASAS domains (patient global assessment of disease activity, pain, function [BASFI], and inflammation [morning stiffness]), with no worsening (deterioration of ≥20%) in any of the remaining domains.

Weeks 8, 12, 16, 24, 36, and 52
Assessment of SpondyloArthritis International Society (ASAS)40 response rate
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Proportion of participants achieving an ASAS40 response, defined as at least 40% improvement from baseline in at least 3 of the 4 ASAS domains, with no worsening in the remaining domain, assessed in the same manner as ASAS20.

Weeks 8, 12, 16, 24, 36, and 52
Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)50 response rate
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Proportion of participants achieving a BASDAI50 response. BASDAI is scored from 0 (no disease activity) to 10 (worst disease activity), with higher scores indicating worse disease activity. BASDAI50 response is defined as at least 50 percent improvement from baseline in BASDAI.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) score
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

BASDAI is scored from 0 (no disease activity) to 10 (worst disease activity), with higher scores indicating worse disease activity.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in Bath Ankylosing Spondylitis Functional Index (BASFI) score
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

BASFI is scored from 0 (no functional limitation) to 10 (worst functional limitation), with higher scores indicating worse physical function.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in Bath Ankylosing Spondylitis Metrology Index (BASMI) score
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

BASMI (linear method) is scored from 0 to 10, with higher scores indicating worse spinal mobility.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in total back pain score
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Total back pain is assessed using a 0-10 numeric rating scale , with higher scores indicating worse back pain.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in participant's global assessment of disease activity (PGA)
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Participant's global assessment of disease activity is assessed using a 0-10 numeric rating scale , with higher scores indicating worse disease activity.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in Maastricht Ankylosing Spondylitis Enthesitis Score (MASES)
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

MASES evaluates 13 enthesal sites, scored from 0 to 13, with higher scores indicating more severe enthesitis.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in Ankylosing Spondylitis Disease Activity Score (ASDAS)
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Change from baseline in Ankylosing Spondylitis Disease Activity Score using C-reactive protein (ASDAS-CRP).ASDAS-CRP is calculated from 5 parameters: total back pain (BASDAI question 2, numeric rating scale [NRS]), participant's global assessment of disease activity, peripheral joint pain/swelling (BASDAI question 3, NRS), duration of morning stiffness (BASDAI question 6, NRS), and serum C-reactive protein (CRP, mg/L). ASDAS-CRP = 0.121 x back pain + 0.058 x duration of morning stiffness + 0.110 x participant global assessment + 0.073 x peripheral joint pain/swelling + 0.579 x Ln(CRP + 1).

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in Assessment of SpondyloArthritis international Society Health Index (ASAS HI) score
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

ASAS HI is scored from 0 to 17, with higher scores indicating worse health status.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in 44-joint swollen joint count
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Swollen joints are assessed in 44 joints, with higher counts indicating more active synovitis.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in dactylitis count
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Dactylitis is assessed as the number of digits with dactylitis, with higher counts indicating more severe dactylitis.

Weeks 8, 12, 16, 24, 36, and 52
Changes from baseline in erythrocyte sedimentation rate (ESR)
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Change from baseline in ESR.

Weeks 8, 12, 16, 24, 36, and 52
Changes from baseline in C-reactive protein (CRP)
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Change from baseline in CRP .

Weeks 8, 12, 16, 24, 36, and 52
Proportion of participants achieving ankylosing spondylitis disease activity score using C-reactive protein (ASDAS-CRP) low disease activity (ASDAS < 2.1) and clinical remission (ASDAS < 1.3)
Időkeret: Weeks 8, 12, 16, 24, 36, and 52

Proportion of participants achieving Ankylosing Spondylitis Disease Activity Score using C-reactive protein (ASDAS-CRP) low disease activity (ASDAS < 2.1) and clinical remission (ASDAS < 1.3). ASDAS-CRP is calculated from participant's global assessment, total back pain, peripheral joint pain/swelling, duration of morning stiffness, and serum C-reactive protein (CRP, mg/L), per the published ASDAS-CRP formula. Higher scores indicate worse disease activity. Disease activity is categorized as: clinical remission, ASDAS < 1.3; low disease activity, ASDAS 1.3 to < 2.1; high disease activity, ASDAS 2.1 to 3.5; very high disease activity, ASDAS > 3.5.

Weeks 8, 12, 16, 24, 36, and 52
Change from baseline in Hospital Anxiety and Depression Scale (HADS) score
Időkeret: Weeks 12, 24, and 52

HADS comprises anxiety and depression subscales, each scored from 0 to 21 (total score 0-42), with higher scores indicating worse anxiety and depression.

Weeks 12, 24, and 52
Change from baseline in Pittsburgh Sleep Quality Index (PSQI) score
Időkeret: Weeks 12, 24, and 52

PSQI global score ranges from 0 to 21, with higher scores indicating worse sleep quality.

Weeks 12, 24, and 52
Changes from baseline in sacroiliac joint inflammation on MRI assessed by the Spondyloarthritis Research Consortium of Canada (SPARCC) score
Időkeret: Weeks 12, 24, and 52

Sacroiliac joint MRI is performed at scheduled visits. Sacroiliac joint inflammation is quantified using the Spondyloarthritis Research Consortium of Canada (SPARCC) sacroiliac joint score (range 0-36, bilateral), with higher scores indicating more severe inflammation.

Weeks 12, 24, and 52
Peak concentration (Cmax) of invariant natural killer T (iNKT) cells in peripheral blood
Időkeret: Weeks 0 to 20
Weeks 0 to 20
Time to peak concentration (Tmax) of iNKT cells in peripheral blood
Időkeret: Weeks 0 to 20
Weeks 0 to 20
Area under the concentration-time curve from time zero to the last measurable concentration (AUC0-t) of iNKT cells in peripheral blood
Időkeret: Weeks 0 to 20
Weeks 0 to 20
Area under the concentration-time curve from time zero to infinity (AUC0-inf) of iNKT cells in peripheral blood
Időkeret: Weeks 0 to 20
Weeks 0 to 20
Half-life (t1/2) of iNKT cells in peripheral blood
Időkeret: Weeks 0 to 20
Weeks 0 to 20
Last detectable concentration (Clast) of iNKT cells in peripheral blood
Időkeret: Weeks 0 to 20
Weeks 0 to 20
Time of last measurable concentration (tlast) of iNKT cells in peripheral blood
Időkeret: Weeks 0 to 20
Weeks 0 to 20
Change from baseline in NK cells (CD3- CD56+)
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Change from baseline in activated NK cells (CD3- CD56+ CD69+)
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Change from baseline in T cells (CD8+)
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Change from baseline in myeloid-derived suppressor cells (MDSCs, CD11b+ CD33+)
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Change from baseline in plasma interferon-gamma (IFN-gamma) concentration
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Change from baseline in plasma tumor necrosis factor-alpha (TNF-alpha) concentration
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Change from baseline in plasma interleukin-6 (IL-6) concentration
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Change from baseline in plasma interleukin-17A (IL-17A) concentration
Időkeret: Weeks 0 to 20 and Weeks 24 and 52
Weeks 0 to 20 and Weeks 24 and 52
Incidence of anti-drug antibodies (ADA) against invariant natural killer T (iNKT) cell surface antigens
Időkeret: Weeks 0, 4, and 12; and at Weeks 24 and 52

Number and percentage of participants with anti-drug antibodies (ADA) against iNKT cell surface antigens (mainly human leukocyte antigen (HLA) class I/II molecules).

Weeks 0, 4, and 12; and at Weeks 24 and 52

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Szponzor

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete (Becsült)

2026. november 1.

Elsődleges befejezés (Becsült)

2028. március 30.

A tanulmány befejezése (Becsült)

2028. március 30.

Tanulmányi regisztráció dátumai

Először benyújtva

2026. október 16.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2026. október 30.

Első közzététel (Tényleges)

2026. november 4.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Tényleges)

2026. november 4.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2026. október 30.

Utolsó ellenőrzés

2026. október 1.

Több információ

A tanulmányhoz kapcsolódó kifejezések

Egyéb vizsgálati azonosító számok

  • GKL006AlloAID01

Terv az egyéni résztvevői adatokhoz (IPD)

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