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- Klinische proef NCT07465289
Een onderzoek naar de evaluatie van de langetermijnveiligheid en werkzaamheid van rozanolixizumab bij volwassen deelnemers met oculaire myasthenia gravis (MyVisionXT)
Een fase 3, open-label, vervolgstudie om de langetermijnveiligheid en werkzaamheid van Rozanolixizumab te evalueren bij volwassen deelnemers met oculaire myasthenia gravis
The purpose of the study is to assess the long-term safety and efficacy of rozanolixizumab in adult study participants with ocular myasthenia gravis.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Fase 3
Contacten en locaties
Studiecontact
- Naam: UCB Cares
- Telefoonnummer: +18445992273
- E-mail: ucbcares@ucb.com
Studie Contact Back-up
- Naam: UCB Cares
- Telefoonnummer: 00184459922733 (UCB)
- E-mail: ucbcares@ucb.com
Studie Locaties
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Beijing, China
- Werving
- Mg0039 31901
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Nanchang, China
- Werving
- Mg0039 31907
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Suzhou, China
- Werving
- Mg0039 31902
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Kobe, Japan
- Werving
- Mg0039 31802
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Barcelona, Spanje
- Werving
- Mg0039 20604
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Madrid, Spanje
- Werving
- Mg0039 20611
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Ohio
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Columbus, Ohio, Verenigde Staten, 43210
- Werving
- Mg0039 10103
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
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Participant must be a minimum of 18 years of age inclusive at the time of signing the informed consent form (ICF)
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Participant must have received at least 1 dose of investigational medicinal product (IMP) (rozanolixizumab or placebo) in MG0038
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Participant for whom the investigator considers a favorable benefit/risk for participation
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Participant who, alone or with assistance of the caregiver, is considered reliable and capable of adhering to the protocol visit schedule or medication intake according to the judgement of the investigator
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Male or female
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A female participant is eligible to participate if she is not, not breastfeeding (including pumping breastmilk to feed a child), and at least 1 of the following conditions applies:
- Not a woman of childbearing potential (WOCBP) OR
- A WOCBP who agrees to follow the contraceptive guidance for the entire study period
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Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICF and in the protocol
Exclusion Criteria:
- Participant meets any of the withdrawal criteria defined in MG0038
- Participant has a clinically relevant active infection (resulting in hospitalization or requiring intravenous (IV) antibiotic treatment) within 6 weeks before study entry.
- Participant intends to have a live vaccination during the study or within 8 weeks following the final dose of rozanolixizumab
- Participant has been administered with the prohibited immunosuppressive medications, biologics, or other therapies
- Participant has planned use of prohibited medications
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Rozanolixizumab
The study is composed of Extended Observation Period(s) and Symptom-driven Cycle(s). Based on their clinical need for treatment, study participants will be able to start the study with either an Extended Observation Period or a Symptom-driven Cycle. A Symptom-driven Cycle will be initiated based on disease worsening and participants will receive rozanolixizumab based on investigator's medical judgement. |
Rozanolixizumab will be administered by subcutaneous infusion.
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Incidence of treatment-emergent adverse events (TEAEs)
Tijdsspanne: Up to 2 years
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Treatment Emergent Adverse Events (TEAEs) are any untoward medical incidence in a participant after the administration of study treatment, whether or not these events are related to study treatment. |
Up to 2 years
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Incidence of treatment-emergent serious adverse events (TESAEs)
Tijdsspanne: Up to 2 years
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An SAE is defined as any untoward medical occurrence that, at any dose, meets 1 or more of the criteria listed:
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Up to 2 years
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Incidence of TEAEs leading to permanent withdrawal of study treatment
Tijdsspanne: Up to 2 years
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Treatment Emergent Adverse Events (TEAEs) are any untoward medical incidence in a participant after the administration of study treatment, whether or not these events are related to study treatment. This measure considers any TEAE leading to permanent withdrawal from study. |
Up to 2 years
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Change from Baseline at Day 43 in (Myasthenia Gravis Impairment Index) MGII ocular score (Patient-Reported Outcome part)
Tijdsspanne: At Day 43 (of the first 3 Symptom-driven Cycles)
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MGII is a measure of disease severity based on the signs and symptoms of MG patients. The MGII has 22 patient-reported items and 6 examination items and scores are presented as a sum of all items for a total score but also as an ocular and generalized sub-score. The scoring range is 0 to 84, 0-23 for the ocular score, and 0-61 for the generalized score, where higher scores are indicative of more severe symptoms. The recall period is "the past week". |
At Day 43 (of the first 3 Symptom-driven Cycles)
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Change from Baseline at Day 43 in Myasthenia Gravis Activities of Daily Living (MG-ADL) ocular score
Tijdsspanne: At Day 43 (of the first 3 Symptom-driven Cycles)
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The MG-ADL score is an 8-item patient-reported outcome (PRO) instrument. The MG-ADL targets symptoms and disability across ocular, bulbar, respiratory, and axial symptoms. The item responses are scored from 0 to 3, and the total score of MG-ADL is the sum of the 8 items and ranges from 0 to 24, with a higher score indicating more disability. The two ocular items will be summed for the ocular score, ranging from 0 to 6. |
At Day 43 (of the first 3 Symptom-driven Cycles)
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Change from Baseline at Day 43 in Myasthenia Gravis Symptoms Patient-Reported Outcome (MGSPRO) ocular muscle weakness scale score
Tijdsspanne: At Day 43 (of the first 3 Symptom-driven Cycles)
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The MG symptoms PRO instrument consisted of 42 items across 5 scales: ocular muscle weakness (items 1-5); bulbar muscle weakness (items 6-15); respiratory muscle weakness (items 16-18); physical fatigue (items 19-33) and muscle weakness fatigability (items 34-42). Only the ocular muscle weakness scale will be used in this study. Ocular symptom severity is assessed over the past 7 days using a 4-point verbal rating scale (none, mild, moderate, severe) |
At Day 43 (of the first 3 Symptom-driven Cycles)
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Change from Baseline at Day 43 in Myasthenia Gravis Quality of Life 15-item Scale (revised version) (MG-QoL15r) total score
Tijdsspanne: At Day 43 (of the first 3 Symptom-driven Cycles)
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The MG-QoL15r is a 15-item PRO measure that is designed to assess aspects of health-related quality of life related to MG. The recall period that will be used is "past 7 days". Each item has 3 response options (0-2) and the total score ranges from 0 to 30, with higher scores indicating more severe impact on health-related QoL (HRQOL). |
At Day 43 (of the first 3 Symptom-driven Cycles)
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Study participant who generalizes to Myasthenia Gravis Foundation of America (MGFA) class ≥2 over time
Tijdsspanne: Up to 2 years
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MGFA Clinical Classification is a 5-stage classification (I to V), with a higher class indicating more severe disease. |
Up to 2 years
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Change from Baseline in MGII total and generalized score over time
Tijdsspanne: Up to 2 years
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MGII is a measure of disease severity based on the signs and symptoms of MG patients. The MGII has 22 patient-reported items and 6 examination items and scores are presented as a sum of all items for a total score but also as an ocular and generalized sub-score. The scoring range is 0 to 84, 0-23 for the ocular score, and 0-61 for the generalized score, where higher scores are indicative of more severe symptoms. The recall period is "the past week". |
Up to 2 years
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Change from Baseline in MG-ADL total score over time
Tijdsspanne: Up to 2 years
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The MG-ADL score is an 8-item patient-reported outcome (PRO) instrument. The MG-ADL targets symptoms and disability across ocular, bulbar, respiratory, and axial symptoms. The item responses are scored from 0 to 3, and the total score of MG-ADL is the sum of the 8 items and ranges from 0 to 24, with a higher score indicating more disability. The two ocular items will be summed for the ocular score, ranging from 0 to 6. |
Up to 2 years
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Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Ziekten van het zenuwstelsel
- Neoplasmata per site
- Neoplasmata
- Neuromusculaire aandoeningen
- Auto-immuunziekten
- Ziekten van het immuunsysteem
- Auto-immuunziekten van het zenuwstelsel
- Neurodegeneratieve ziekten
- Paraneoplastische syndromen, zenuwstelsel
- Neoplasmata van het zenuwstelsel
- Paraneoplastische syndromen
- Neuromusculaire junctieziekten
- Myasthenia Gravis
- rozanolixizumab
Andere studie-ID-nummers
- MG0039
- 2025-524757-14-00 (Ctis)
- U1111-1334-3218 (Andere identificatie: Universal Trial Number)
- CTR20262521 (Register-ID: ChinaDrugTrials.org.cn)
- 2025 (Subsidie/contract van de Amerikaanse NIH)
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
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 pre-specified 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.
IPD-tijdsbestek voor delen
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.
IPD-toegangscriteria voor delen
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.
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
- MVO
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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