Efficacy and Safety of Adalimumab for the Treatment of Ocular Inflammation (PANDA-U)
Efficacy and Safety of Adalimumab in Pediatric Non-Infectious Uveitis: A Multicenter Ambispective Single-Arm Clinical Trial
This study aims to evaluate the clinical efficacy and safety of adalimumab in pediatric non-infectious uveitis and to generate domestic real-world evidence (RWE), thereby establishing a clinical foundation for label expansion and reimbursement coverage.
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Detaillierte Beschreibung
Background: Although anti-TNFα agents play a crucial role globally in managing refractory non-infectious uveitis, adalimumab was removed from the approved indication for pediatric uveitis in South Korea several years ago-unlike adult uveitis-making domestic prescription exceptionally difficult. Meanwhile, indications for pediatric idiopathic arthritis and pediatric Crohn's disease remain approved domestically, highlighting an urgent need to establish objective evidence to resolve this regulatory discrepancy. Furthermore, as a substantial number of pediatric patients in Korea are already receiving off-label, non-reimbursed adalimumab treatment, their real-world data serve both as evidence of efficacy and safety and as direct proof of this institutional imbalance.
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: mieun kim
- Telefonnummer: +82-2-2148-7664
- E-Mail: mieun2728.kim@samsung.com
Studienorte
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Seoul, Südkorea, 06351
- Samsung Medical Center
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Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
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For the Prospective New-User Cohort, verification of Inclusion Criteria 1 through 6 is required.
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For the Retrospective (Switch) Cohort, verification of Inclusion Criteria 1 through 7 is required.
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Pediatric patients aged 2 years and < 18 years.
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Diagnosed with non-infectious anterior uveitis, intermediate uveitis, posterior uveitis, or panuveitis.
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Active intraocular inflammation demonstrated by anterior chamber (AC) cell grade ≥ 1+ (defined as 6 cells per 1 mm\times 1 mm field) according to the SUN (Standardization of Uveitis Nomenclature) criteria, or active posterior segment lesions persistently observed on at least two consecutive assessments despite 12 weeks of treatment with methotrexate and corticosteroids (systemic or topical) prior to screening (SUN grade maintained on 2 occasions, adapted from the SYCAMORE trial definition of active disease).
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Inadequate response to corticosteroid therapy or other immunosuppressive agents (e.g., methotrexate [MTX]), or inability to continue treatment due to unacceptable toxicity/intolerance.
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Written informed consent obtained from the subject's legal representative (parent or legal guardian) and written pediatric assent obtained according to applicable age-specific regulatory and institutional guidelines.
[Prospective De Novo Cohort]
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Patients initiating adalimumab for the first time (adalimumab-naïve).
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[Retrospective / Prospective Cohort] 6. Patients currently on maintenance therapy with adalimumab (including extended dosing intervals, such as every other week [Q2W] or every 3-4 weeks) who require at least 1 additional year of treatment.
7. Patients who agree to switch to the investigational product and adhere to a standard every-other-week (Q2W / once every 2 weeks) administration schedule at the time of study enrollment.
Exclusion Criteria:
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For the Prospective New-User Cohort, verification of Exclusion Criteria 1 through 22 is required.
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For the Retrospective (Switch) Cohort, verification of Exclusion Criteria 1 through 24 is required.
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Patients with uveitis associated with juvenile idiopathic arthritis (JIA) or pediatric Crohn's disease indicated for adalimumab
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Individuals with infectious uveitis or non-immunological intraocular inflammation resulting from trauma, surgery, etc., within 30 days prior to screening
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Individuals with active tuberculosis, untreated latent tuberculosis, sepsis, opportunistic infections, or other severe active infections, or those at high risk for such infections
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Individuals with a history of hypersensitivity to adalimumab or any of its excipients
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Individuals instilling topical glucocorticoids more than 6 times per eye per day, or currently receiving oral prednisone (or its equivalent) at a dose exceeding 0.2 mg/kg/day (adapted from the SYCAMORE criteria)
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Individuals with active malignancy, lymphoproliferative disorders, demyelinating disease (e.g., multiple sclerosis, Guillain-Barré syndrome), or a history of other progressive or degenerative neurological disorders
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Patients who have received TNF inhibitors other than the investigational product
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Patients with New York Heart Association (NYHA) Class III/IV cardiac disease
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Individuals with uncontrolled viral infections, including active hepatitis B or hepatitis C
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Individuals who have received a live vaccine (including live-attenuated vaccines) within 30 days prior to screening, or who are scheduled to receive one during the study period
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Individuals who are pregnant or breastfeeding, or women of childbearing potential (WOCBP) who do not agree to use highly effective contraception*
*A highly effective method of contraception is defined as one that results in a low failure rate of less than 1% per year when used consistently and correctly, and includes: combined (estrogen- and progestogen-containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal); progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable); intrauterine device (IUD); intrauterine hormone-releasing system (IUS); bilateral tubal occlusion; vasectomized partner; and sexual abstinence.
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Individuals who have received other biologic agents within 5 half-lives prior to screening
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Individuals with a family member who has active tuberculosis, or who have a history of close contact with an individual with active tuberculosis
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Individuals with a major infection requiring antibiotic therapy within 30 days prior to screening
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Individuals with diabetes mellitus deemed uncontrolled by the investigator, or persistently uncontrolled severe hypertension (> 95th percentile for height and age)
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Individuals with a history of malignancy, or a history of solid organ, bone marrow, or corneal transplantation
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Individuals with a history of ocular surgery (e.g., cataract surgery) within 3 months prior to screening
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Individuals who have received intraocular or periocular corticosteroid injections within 30 days prior to screening
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Individuals with a history of ocular herpes simplex or herpes zoster infection
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Individuals with laboratory values evaluated during screening that meet any of the following criteria:
A. Hemoglobin < 8.0 g/dL B. WBC < 4.0 × 10³/µL C. ANC < 1.0 × 10³/µL D. Platelet count < 100 × 10³/µL E. AST or ALT > 2 × ULN
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Individuals weighing less than 15 kg
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Individuals otherwise deemed unsuitable for study participation in the judgment of the investigator
[Retrospective / Prospective Cohort-Specific Criteria]
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Inability to confirm disease activity (e.g., SUN grading) at the initial start of adalimumab treatment and subsequent treatment response via medical record review.
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Patients whose adalimumab dosage has been tapered to near-discontinuation (i.e., dosing intervals substantially exceeding once every 4 weeks) or for whom the treating physician deems the standard maintenance regimen (once every 2 weeks) clinically inappropriate.
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Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
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Experimental: Prospective and Retrospective (Switch) Cohorts
Prospective Cohort: Adalimumab-naïve patients will receive the investigational product (an adalimumab biosimilar) for 12 months (approximately 52 weeks) after enrollment. Retrospective (Switch) Cohort: Adalimumab-experienced patients who require at least 1 additional year of treatment will switch to the investigational product at enrollment. |
The adalimumab biosimilar is administered via subcutaneous (SC) injection with weight-tiered dosing (<30 kg: 20 mg; ≥30 kg: 40 mg) every two weeks (q2w) as a maintenance dose-for 52 weeks in the prospective cohort and for at least 12 months in the retrospective (switch) cohort. |
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Treatment Failure Rate in the Prospective Treatment-Naïve Cohort
Zeitfenster: Up to 12 months after adalimumab initiation
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Percentage of participants meeting the criteria for treatment failure. Treatment failure is defined as any of the following: active intraocular inflammation (worsening anterior chamber cell grade, vitreous haze, or new chorioretinal lesions), lack of clinical efficacy requiring addition of new systemic immunosuppressive agents, inability to taper concomitant systemic corticosteroids to target maintenance levels, or discontinuation of the investigational product due to lack of efficacy or unacceptable toxicity. |
Up to 12 months after adalimumab initiation
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Change from Baseline in Medically Important Infections (MIIS) in the Prospective Treatment-Naïve Cohort
Zeitfenster: Baseline and 12 months after adalimumab initiation
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Total count and incidence rate of Medically Important Infections (defined as opportunistic infections, infections requiring intravenous antimicrobial therapy, or infections resulting in hospitalization or death) observed per participant. The change is calculated as the incidence during the 12-month post-initiation period compared to the pre-baseline reference status. |
Baseline and 12 months after adalimumab initiation
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Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Treatment Failure Rate in the Retrospective (Switch) Cohort
Zeitfenster: Up to 12 months post-switch to the investigational product
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Percentage of participants who experience treatment failure following switch to the investigational product. Treatment failure is defined as active intraocular inflammation, necessity to escalate therapy or introduce unpermitted rescue therapies, or drug discontinuation due to lack of efficacy or adverse events. |
Up to 12 months post-switch to the investigational product
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Relapse-Free Survival Rate in the Retrospective (Switch) Cohort
Zeitfenster: At 12, 24, and 36 months post-adalimumab initiation
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Percentage of participants maintaining clinical inactive disease without uveitis recurrence after achieving initial clinical response, estimated using Kaplan-Meier survival methodology at specified annual landmark intervals. |
At 12, 24, and 36 months post-adalimumab initiation
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Cumulative Incidence of Relapse and Management Strategies in the Retrospective (Switch) Cohort
Zeitfenster: Up to 36 months post-adalimumab initiation
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Cumulative incidence of ocular relapse and the distribution of clinical management strategies implemented upon relapse, categorized as dose escalation, administration interval shortening (e.g., from every other week to weekly), or permanent treatment discontinuation. |
Up to 36 months post-adalimumab initiation
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Drug Survival Rate of Adalimumab in the Retrospective (Switch) Cohort
Zeitfenster: Up to 36 months post-adalimumab initiation
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Percentage of participants remaining on adalimumab therapy over time without permanent treatment cessation, evaluated by Kaplan-Meier survival curves. |
Up to 36 months post-adalimumab initiation
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Time to Adalimumab Discontinuation in the Retrospective (Switch) Cohort
Zeitfenster: Up to 36 months post-adalimumab initiation
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Median time (in months) from adalimumab initiation to permanent discontinuation of therapy due to any reason, including loss of response, remission, adverse events, or patient withdrawal. |
Up to 36 months post-adalimumab initiation
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Steroid-Sparing Success Rate in the Retrospective (Switch) Cohort (Pooled Analysis)
Zeitfenster: Up to 36 months post-adalimumab initiation
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Percentage of participants achieving successful systemic steroid-sparing, defined as achieving disease inactivity with oral prednisone (or equivalent) tapered to $\le 0.1\text{ mg/kg/day}$ (or complete cessation) and topical glucocorticoids tapered to $\le 2\text{ drops/day/eye}$. |
Up to 36 months post-adalimumab initiation
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Change from Baseline in Systemic and Topical Corticosteroid Requirements in the Retrospective (Switch) Cohort
Zeitfenster: Baseline (initial adalimumab start) and up to 36 months post-initiation
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Quantitative reduction in daily systemic corticosteroid dose (mg/kg/day of prednisone equivalent) and change in daily frequency of topical ophthalmic corticosteroid instillations per affected eye. |
Baseline (initial adalimumab start) and up to 36 months post-initiation
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Cumulative Incidence of Cataract and Elevated Intraocular Pressure in the Retrospective (Switch) Cohort (Pooled Analysis)
Zeitfenster: Up to 36 months post-adalimumab initiation
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Percentage of participants who develop new-onset or worsening cataract (requiring surgical intervention or clinically significant progression) or elevated intraocular pressure ($\text{IOP} > 21\text{ mmHg}$ or an increase $\ge 10\text{ mmHg}$ from baseline requiring hypotensive medication). |
Up to 36 months post-adalimumab initiation
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Andere Ergebnismessungen
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Integrated Assessment of Adverse Events Across the Cumulative Exposure Period
Zeitfenster: Up to 48 months (covering up to 36 months retrospective exposure plus 12 months prospective study period)
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Number, incidence rates, and severity of treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), and adverse drug reactions (ADRs) assessed per Common Terminology Criteria for Adverse Events (CTCAE) criteria across the combined follow-up duration. |
Up to 48 months (covering up to 36 months retrospective exposure plus 12 months prospective study period)
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Mitarbeiter
Mitarbeiter
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- 2026-08-116
Plan für individuelle Teilnehmerdaten (IPD)
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Beschreibung des IPD-Plans
Individual participant data (IPD) will not be shared publicly to protect patient privacy and comply with relevant personal information protection regulations. Summary data and study results will be made available through peer-reviewed publication.
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