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| ID | Type | Description | Link |
|---|---|---|---|
| 2019-003409-83 | EudraCT Number | ||
| U1111-1293-7098 | Other Identifier | World Health Organization (WHO) | |
| 2023-506368-14 | Registry Identifier | EU Clinical Trials |
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The purpose of this study is to evaluate long-term safety and tolerability of dapirolizumab pegol treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Dapirolizumab pegol | Experimental | Subjects will receive dapriolizumab pegol throughout the Treatment Period. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Dapirolizumab pegol | Drug | Subjects will receive dapirolizumab pegol at prespecified time-points. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of treatment-emergent adverse events (TEAEs) during the study | Treatment-emergent adverse events (TEAEs) are any untoward medical incidence in a subject during administered study treatment, whether or not these events are related to study treatment. | From Baseline (Day 1) until Safety Follow-Up (up to Week 110) |
| Incidence of serious treatment-emergent adverse events during the study | A serious treatment-emergent adverse event (serious TEAE) is any untoward medical occurrence that at any dose:
| From Baseline (Day 1) until Safety Follow-Up (up to Week 110) |
| Incidence of treatment-emergent adverse events (TEAEs) leading to permanent dapirolizumab pegol discontinuation | Treatment-emergent adverse events (TEAEs) are any untoward medical incidence in a subject during administered study treatment, and leading to permanent drug discontinuation whether or not these events are related to study treatment. | From Baseline (Day 1) until Safety Follow-Up (up to Week 110) |
| Measure | Description | Time Frame |
|---|---|---|
| Achievement of prevention of severe BILAG flares (severe BILAG flare-free) through Week 24 | BILAG severe flare is defined as a new British Isles Lupus Assessment Group Disease Activity Index 2004 (BILAG 2004) Grade A since previous visit in any system due to individual items that are new or worse qualifying for the Grade A (Isenberg et al, 2011). Determination of items that are new or worse qualifying for the Grade A will be according to the supplementary information for the numerical scoring of the BILAG-2004 index (Yee et al, 2010). |
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Inclusion Criteria:
Exclusion Criteria:
- Study participant has any medical or psychiatric condition (including conditions due to neuropsychiatric systemic lupus erythematosus (SLE)) that, in the opinion of the Investigator, could jeopardize or would compromise the study participant's ability to participate in this study. This includes study participants with a life-threatening condition or ongoing malignancies at the start of the study
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| Name | Affiliation | Role |
|---|---|---|
| UCB Cares | 001 844 599 2273 (UCB) | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sl0046 50140 | Birmingham | Alabama | 35294 | United States | ||
| Sl0046 50058 |
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.
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.
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.
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| Week 24 |
| Achievement of prevention of severe BILAG flares (severe BILAG flare-free) through Week 52 | BILAG severe flare is defined as a new British Isles Lupus Assessment Group Disease Activity Index 2004 (BILAG 2004) Grade A since previous visit in any system due to individual items that are new or worse qualifying for the Grade A (Isenberg et al, 2011). Determination of items that are new or worse qualifying for the Grade A will be according to the supplementary information for the numerical scoring of the BILAG-2004 index (Yee et al, 2010). | Week 52 |
| Achievement of prevention of severe BILAG flares (severe BILAG flare-free) through Week 104 | BILAG severe flare is defined as a new British Isles Lupus Assessment Group Disease Activity Index 2004 (BILAG 2004) Grade A since previous visit in any system due to individual items that are new or worse qualifying for the Grade A (Isenberg et al, 2011). Determination of items that are new or worse qualifying for the Grade A will be according to the supplementary information for the numerical scoring of the BILAG-2004 index (Yee et al, 2010). | Week 104 |
| Achievement of LLDAS at ≥50% of all visits | Low lupus disease activity state (LLDAS) is defined as:
| From Baseline (Day 1) until End of Treatment (Week 104) |
| Achievement of BICLA response at Week 24 | A study participant is considered to be a BILAG 2004-based Composite Lupus Assessment (BICLA) responder if all of the following is fulfilled:
The parent studies Baseline will be used as reference point. | Week 24 |
| Achievement of BICLA response at Week 52 | A study participant is considered to be a BICLA responder if all of the following is fulfilled:
The parent studies Baseline will be used as reference point. | Week 52 |
| Achievement of BICLA response at Week 104 | A study participant is considered to be a BICLA responder if all of the following is fulfilled:
The parent studies Baseline will be used as reference point. | Week 104 |
| Avondale |
| Arizona |
| 85392 |
| United States |
| Sl0046 50328 | Tucson | Arizona | 85704 | United States |
| Sl0046 50383 | Beverly Hills | California | 90210 | United States |
| Sl0046 50275 | La Palma | California | 90623-1730 | United States |
| Sl0046 50316 | San Leandro | California | 94578 | United States |
| Sl0046 50339 | Denver | Colorado | 80230 | United States |
| Sl0046 50239 | Brandon | Florida | 33511 | United States |
| Sl0046 50362 | Gainesville | Florida | 32610 | United States |
| Sl0046 50681 | Miami | Florida | 33172 | United States |
| Sl0046 50059 | Ormond Beach | Florida | 32174 | United States |
| Sl0046 50324 | Plantation | Florida | 33324 | United States |
| Sl0046 50329 | Tampa | Florida | 33606 | United States |
| Sl0046 50698 | Tampa | Florida | 33618 | United States |
| Sl0046 50368 | Atlanta | Georgia | 30303 | United States |
| Sl0046 50240 | Idaho Falls | Idaho | 83404 | United States |
| Sl0046 50474 | Hopkinsville | Kentucky | 42240-1746 | United States |
| Sl0046 50285 | Lake Charles | Louisiana | 70605 | United States |
| Sl0046 50015 | Hagerstown | Maryland | 21740 | United States |
| Sl0046 50219 | Detroit | Michigan | 48201 | United States |
| Sl0046 50273 | Las Vegas | Nevada | 89128 | United States |
| Sl0046 50366 | Canton | New York | 13617 | United States |
| Sl0046 50264 | Manhasset | New York | 11030 | United States |
| Sl0046 50334 | New York | New York | 10032 | United States |
| Sl0046 50238 | Charlotte | North Carolina | 28211 | United States |
| Sl0046 50147 | Hershey | Pennsylvania | 17033 | United States |
| Sl0046 50001 | Jackson | Tennessee | 38305 | United States |
| Sl0046 50418 | Colleyville | Texas | 76034 | United States |
| Sl0046 50050 | Beckley | West Virginia | 25801 | United States |
| Sl0046 60002 | Buenos Aires | Argentina |
| Sl0046 60029 | Mendoza | Argentina |
| Sl0046 60003 | Quilmes | Argentina |
| Sl0046 60022 | Quilmes | Argentina |
| Sl0046 60011 | San Juan | Argentina |
| Sl0046 60014 | San Miguel de Tucumán | Argentina |
| Sl0046 40123 | Brussels | Belgium |
| Sl0046 40189 | Plovdiv | Bulgaria |
| Sl0046 40380 | Sofia | Bulgaria |
| Sl0046 50374 | Calgary | Canada |
| Sl0046 50337 | Edmonton AB | Canada |
| Sl0046 50259 | Rimouski | Canada |
| Sl0046 50045 | Toronto | Canada |
| Sl0046 60015 | Santiago | Chile |
| Sl0046 60018 | Santiago | Chile |
| Sl0046 20291 | Changchun | China |
| Sl0046 20019 | Guangzhou | China |
| Sl0046 20290 | Guilin | China |
| Sl0046 20020 | Shanghai | China |
| Sl0046 20136 | Tianjin | China |
| Sl0046 20025 | Wenzhou | China |
| Sl0046 20180 | Wuhan | China |
| Sl0046 20132 | Zhengzhou | China |
| Sl0046 60013 | Barranquilla | Colombia |
| Sl0046 60019 | Barranquilla | Colombia |
| Sl0046 60006 | Bogotá | Colombia |
| Sl0046 60027 | Bogotá | Colombia |
| Sl0046 60016 | Bucaramanga | Colombia |
| Sl0046 60007 | Chía | Colombia |
| Sl0046 60031 | Montería | Colombia |
| Sl0046 40066 | Prague | Czechia |
| Sl0046 40386 | Cologne | Germany |
| Sl0046 40072 | Freiburg im Breisgau | Germany |
| Sl0046 40027 | Herne | Germany |
| Sl0046 40078 | Leipzig | Germany |
| Sl0046 40402 | Tübingen | Germany |
| Sl0046 40715 | Vogelsang-gommern | Germany |
| Sl0046 40378 | Athens | Greece |
| Sl0046 40501 | Athens | Greece |
| Sl0046 40377 | Crete | Greece |
| Sl0046 40507 | Larissa | Greece |
| Sl0046 40412 | Budapest | Hungary |
| Sl0046 40411 | Debrecen | Hungary |
| Sl0046 40031 | Szeged | Hungary |
| Sl0046 40499 | Székesfehérvár | Hungary |
| Sl0046 40084 | Catania | Italy |
| Sl0046 40448 | Milan | Italy |
| Sl0046 20030 | Chūōku | Japan |
| Sl0046 20287 | Nagoya | Japan |
| Sl0046 50317 | Chihuahua City | Mexico |
| Sl0046 50250 | Cuernavaca | Mexico |
| Sl0046 50249 | Guadalajara | Mexico |
| Sl0046 50271 | León | Mexico |
| Sl0046 50252 | Mérida | Mexico |
| Sl0046 50251 | Monterrey | Mexico |
| Sl0046 60009 | Lima | Peru |
| Sl0046 60023 | Lima | Peru |
| Sl0046 20182 | Davao City | Philippines |
| Sl0046 20181 | Makati | Philippines |
| Sl0046 40482 | Bialystok | Poland |
| Sl0046 40119 | Bydgoszcz | Poland |
| Sl0046 40398 | Katowice | Poland |
| Sl0046 40502 | Krakow | Poland |
| Sl0046 40151 | Lublin | Poland |
| Sl0046 40044 | Poznan | Poland |
| Sl0046 40090 | Poznan | Poland |
| Sl0046 40097 | Warsaw | Poland |
| Sl0046 40098 | Warsaw | Poland |
| Sl0046 40397 | Wroclaw | Poland |
| Sl0046 40481 | Wroclaw | Poland |
| Sl0046 50671 | Caguas | Puerto Rico |
| Sl0046 40382 | Galati | Romania |
| Sl0046 40393 | Belgrade | Serbia |
| Sl0046 40461 | Belgrade | Serbia |
| Sl0046 20108 | Incheon | South Korea |
| Sl0046 20104 | Seoul | South Korea |
| Sl0046 40160 | Barcelona | Spain |
| Sl0046 40341 | Málaga | Spain |
| Sl0046 40101 | Sabadell | Spain |
| Sl0046 40099 | Vigo | Spain |
| Sl0046 20113 | Taichung | Taiwan |
| Sl0046 20142 | Taichung | Taiwan |
| Sl0046 20095 | Taipei | Taiwan |
| Sl0046 20082 | Taiyuan | Taiwan |
| ID | Term |
|---|---|
| D008180 | Lupus Erythematosus, Systemic |
| ID | Term |
|---|---|
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
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| ID | Term |
|---|---|
| C000607972 | dapirolizumab pegol |
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