Badanie mające na celu ocenę skuteczności i bezpieczeństwa rozanoliksyzumabu u dorosłych uczestników z chorobą związaną z przeciwciałami przeciwko glikoproteinie oligodendrocytów mieliny (MOG) (MOG-AD) (cosMOG)
Randomizowane, podwójnie ślepe, kontrolowane placebo, wieloośrodkowe, kluczowe badanie fazy 3 z przedłużonym okresem otwartej próby w celu oceny skuteczności i bezpieczeństwa rozanoliksyzumabu u dorosłych uczestników z chorobą związaną z przeciwciałami przeciw glikoproteinie oligodendrocytów mieliny (MOG) (MOG- OGŁOSZENIE)
The purpose of the study is to evalute the efficacy, safety and tolerability of rozanolixizumab for treatment of adult participants with myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD).
Przegląd badań
Status
Interwencja / Leczenie
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Faza 3
Kontakty i lokalizacje
Lokalizacje studiów
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Melbourne, Australia
- Mog001 30022
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Ghent, Belgia
- Mog001 40185
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Porto Alegre, Brazylia
- Mog001 60033
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Hradec Králové, Czechy
- Mog001 40195
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Teplice, Czechy
- Mog001 40721
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Strasbourg, Francja
- Mog001 40170
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Athens, Grecja
- Mog001 40850
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Barcelona, Hiszpania
- Mog001 40267
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Madrid, Hiszpania
- Mog001 40161
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Murcia, Hiszpania
- Mog001 40350
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Málaga, Hiszpania
- Mog001 40341
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Seville, Hiszpania
- Mog001 40049
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Chiba, Japonia
- Mog001 20068
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Isehara, Japonia
- Mog001 20307
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Kitakyushu-shi, Japonia
- Mog001 20049
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Kodaira, Japonia
- Mog001 20143
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Koriyama-shi, Japonia
- Mog001 20223
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Sendai, Japonia
- Mog001 20224
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Sendai, Japonia
- Mog001 20227
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Shinjuku-ku, Japonia
- Mog001 20070
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Suita-shi, Japonia
- Mog001 20032
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Goyang-si, Korea Południowa
- Mog001 20226
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Culiacán, Meksyk
- Mog001 50486
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Mexico City, Meksyk
- Mog001 50485
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Göttingen, Niemcy
- Mog001 40140
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Münster, Niemcy
- Mog001 40177
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Bydgoszcz, Polska
- Mog001 40840
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Coimbra, Portugalia
- Mog001 40485
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Porto, Portugalia
- Mog001 40669
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Arizona
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Scottsdale, Arizona, Stany Zjednoczone, 85259-5452
- Mog001 50297
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California
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Palo Alto, California, Stany Zjednoczone, 94304
- Mog001 50450
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Colorado
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Aurora, Colorado, Stany Zjednoczone, 80045
- Mog001 50101
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District of Columbia
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Washington D.C., District of Columbia, Stany Zjednoczone, 20057
- Mog001 50553
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Florida
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Tampa, Florida, Stany Zjednoczone, 33612
- Mog001 50308
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Illinois
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Peoria, Illinois, Stany Zjednoczone, 61637
- Mog001 50472
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Maryland
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Baltimore, Maryland, Stany Zjednoczone, 21287
- Mog001 50552
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Massachusetts
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Boston, Massachusetts, Stany Zjednoczone, 02114-3117
- Mog001 50243
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Minnesota
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Rochester, Minnesota, Stany Zjednoczone, 55905
- Mog001 50104
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Texas
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San Antonio, Texas, Stany Zjednoczone, 78229
- Mog001 50568
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Utah
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Salt Lake City, Utah, Stany Zjednoczone, 84112
- Mog001 50473
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Basel, Szwajcaria
- Mog001 40723
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Bern, Szwajcaria
- Mog001 40337
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Zurich, Szwajcaria
- Mog001 40630
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Huddinge, Szwecja
- Mog001 40663
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Istanbul, Turcja (Türkiye)
- Mog001 40550
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Izmir, Turcja (Türkiye)
- Mog001 40726
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Samsun, Turcja (Türkiye)
- Mog001 40648
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Sancaktepe, Turcja (Türkiye)
- Mog001 40725
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Kyiv, Ukraina
- Mog001 20319
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Ternopil, Ukraina
- Mog001 20228
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Pavia, Włochy
- Mog001 40146
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Roma, Włochy
- Mog001 40629
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Verona, Włochy
- Mog001 40646
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Liverpool, Zjednoczone Królestwo
- Mog001 40661
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Oxford, Zjednoczone Królestwo
- Mog001 40163
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Participant must be ≥18 to ≤89 years of age, at the time of signing the informed consent
- Confirmed diagnosis of MOGAD consistent with published diagnostic criteria for MOGAD
- Participant has history of relapsing MOGAD with at least 1 documented relapse over the last 12 months and a documented positive serum MOG Ab test using a cell-based assay (CBA) within 6 months prior to randomization
- Participant must be clinically stable at the time of the Screening Visit and during the Screening Period
Exclusion Criteria:
- Participant has been diagnosed with a neurological autoimmune disease (including multiple sclerosis (MS) and aquaporin-4 positive neuromyelitis optica spectrum disorder (NMOSD)), or a systemic autoimmune disease that in the opinion of the investigator can interfere with the safety of the participant
- Participant has a clinically important active infection (including unresolved or not adequately treated infection) as assessed by the investigator, including participants with a serious infection within 6 weeks prior to the first dose of the investigational medicinal product (IMP)
- Participant has a current or medical history of primary immunodeficiency
- Participant tests positive for aquaporin-4 antibodies at Screening
- Participant has a serum total IgG level ≤ 5.5g/L
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Poczwórny
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Rozanolixizumab Arm
Participants randomized into this arm will receive rozanolixizumab at pre-specified timepoints. |
Participants will receive pre-specified doses of rozanolixizumab.
Inne nazwy:
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Komparator placebo: Placebo Arm
Participants randomized into this arm will receive placebo at pre-specified timepoints to maintain the blinding. |
Participants will receive placebo.
Inne nazwy:
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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For Part A: Time from randomization to first independently centrally adjudicated relapse (TTFR) during the DB Treatment Period
Ramy czasowe: Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
|
The TTFR (days) will be defined as the interval between the date of randomization and the first date of the objective relapse. During the Double Blind (DB) Treatment Period (Part A); EDB/EWD = End of Double-Blind/Early Withdrawal Visit |
Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
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For Part B: Incidence of treatment-emergent adverse events (TEAEs) during OLE Treatment Period
Ramy czasowe: OLE Treatment Period (OLE Week 1) to EOS/EWD Visit (up to OLE Week 52)
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An adverse event (AE) is any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of investigational medicinal product (IMP), whether or not considered related to the IMP. NOTE: An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of IMP. Open-Label Extension (OLE) Treatment Period (Part B); EOS/EWD = End of Study/Early Withdrawal Visit. |
OLE Treatment Period (OLE Week 1) to EOS/EWD Visit (up to OLE Week 52)
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For Part B: Incidence of treatment-emergent adverse events (TEAEs) leading to permanent withdrawal of investigational medicinal product (IMP) during OLE Treatment Period
Ramy czasowe: OLE Treatment Period (OLE Week 1) to EOS/EWD Visit (up to OLE Week 52)
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An adverse event (AE) is any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of investigational medicinal product (IMP), whether or not considered related to the IMP. NOTE: An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of IMP. TEAEs leading to discontinuation of the study are reported. |
OLE Treatment Period (OLE Week 1) to EOS/EWD Visit (up to OLE Week 52)
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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For Part A: Change from Baseline in Low-Contrast Monocular Visual Acuity (Worst Affected Eye) measured by low-contrast Landolt C Broken Rings Chart at the EDB/EWD Visit
Ramy czasowe: Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
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Visual acuity is a measurement of the capacity for visual discrimination of fine details. Visual acuity tests are used to determine the smallest characters that can be read on a standardized chart. The Landolt C Broken Ring Chart uses standardized incomplete rings or "C", which are positioned in any direction in the chart (up, down, left, right, and 45 degree positions in between). The participant has to be able to indicate where the break of the "C" is located, by describing the position or by giving gesture. |
Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
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For Part A: Disability as assessed by Expanded Disability Status Scale (EDSS) scores at the EDB/EWD Visit (with confirmation at 3 months)
Ramy czasowe: Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
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The EDSS is an ordinal clinical rating scale ranging from 0 (normal neurologic examination) to 10 (death) in half-point increments with half steps from 1.0 to 9.5. The higher the value the higher is the level of impairment and disability. |
Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
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For Part A: Number of MOGAD related inpatient hospitalizations during the DB Treatment Period
Ramy czasowe: Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
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The total number of MOGAD related hospitalizations from Baseline through EDB/EWD Visit. |
Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
|
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For Part A: Incidence of treatment-emergent adverse events (TEAEs) during the DB Treatment Period
Ramy czasowe: Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
|
An adverse event (AE) is any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of investigational medicinal product (IMP), whether or not considered related to the IMP. NOTE: An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of IMP. |
Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
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For Part B: Independently centrally adjudicated annualized relapse rate (ARR) during the DB and OLE Treatment Period
Ramy czasowe: Baseline (Week 1) to EOS/EWD Visit (up to OLE Week 52)
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An ARR will be calculated for each participant prior to randomization into the Double-Blind Treatment Period (based on available historical data), and 2 ARRs after randomization to study treatment: first for relapses occurring during the Double-Blind Treatment Period and the second for relapses occurring during the OLE Treatment Period. The relapse episodes for each participant will be recorded throughout the entire study. |
Baseline (Week 1) to EOS/EWD Visit (up to OLE Week 52)
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Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: UCB Cares, 001 844 599 2273
Publikacje i pomocne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- MOG001
- 2021-000352-19 (Numer EudraCT)
- 2023-509237-39 (Identyfikator rejestru: EU Clinical Trials)
- U1111-1301-0122 (Inny identyfikator: Universal Trial Number (UTN))
- 2023 (Grant/umowa NIH USA)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Data from this trial may be requested by qualified researchers six months after product approval in the US and/or Europe, or global development is discontinued, and 18 months after trial completion. Investigators may request access to anonymized individual patient-level data and redacted trial documents which may include: analysis-ready datasets, study protocol, annotated case report form, statistical analysis plan, dataset specifications, and clinical study report. Prior to use of the data, proposals need to be approved by an independent review panel at www.Vivli.org and a signed data sharing agreement will need to be executed. All documents are available in English only, for a prespecified time, typically 12 months, on a password protected portal. This plan may change if the risk of re-identifying trial participants is determined to be too high after the trial is completed; in this case and to protect participants, individual patient-level data would not be made available.
Ramy czasowe udostępniania IPD
Data from this trial may be requested by qualified researchers six months after product approval in the US and/or Europe or global development is discontinued, and 18 months after trial completion.
Kryteria dostępu do udostępniania IPD
Qualified researchers may request access to anonymized IPD and redacted study documents which may include: raw datasets, analysis-ready datasets, study protocol, blank case report form, annotated case report form, statistical analysis plan, dataset specifications, and clinical study report. Prior to use of the data, proposals need to be approved by an independent review panel at www.Vivli.org and a signed data sharing agreement will need to be executed.All documents are available in English only, for a pre-specified time, typically 12 months, on a password protected portal.
Typ informacji pomocniczych dotyczących udostępniania IPD
- PROTOKÓŁ BADANIA
- SOK ROŚLINNY
- CSR
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
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