BENLYSTA® 특수 약물 사용 조사
2026년 4월 24일 업데이트: GlaxoSmithKline
정맥 주사 / 피하 주사 특수 약물 사용 조사를위한 BENLYSTA
본 연구의 목적은 일상 임상에서 Benlysta 정맥주사 및 피하주사 Benlysta(이하 "Benlysta")의 장기 안전성 및 유효성에 대한 정보를 수집하고 평가하는 것이다.
Benlysta 시판 후 일정 수의 피험자로부터 데이터가 축적될 때까지 모든 피험자를 대상으로 약물 사용 조사(DUI)를 실시하는 것을 목적으로 Benlysta의 안전성과 유효성에 대한 데이터를 조기에 수집하여 필요한 조치를 취하는 것입니다. Benlysta의 올바른 사용을 위해.
약 600명의 피험자가 이 연구에 등록할 것입니다.
피험자별 관찰 기간은 벤리스타 투여 시작일로부터 52주이다.
BENLYSTA는 GlaxoSmithKline(GSK) 그룹 회사의 등록 상표입니다.
연구 개요
연구 유형
관찰
등록 (실제)
1514
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Hiroshima, 일본, 730-0001
- GSK Investigational Site
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 어린이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
아니
샘플링 방법
확률 샘플
연구 인구
이 연구에는 Benlysta가 투여되는 모든 피험자가 포함됩니다.
또한, 출시 후 투여를 시작하는 대상자 중에는 계약 체결 이전에 이미 벤리스타가 투여한 대상자 및 병원 이송 등으로 진단 시 이미 투여를 시작한 대상자도 포함된다.
설명
포함 기준:
- 이 연구에는 Benlysta가 투여되는 모든 피험자가 포함됩니다. 또한, 출시 후 투여를 시작하는 대상자 중에는 계약 체결 이전에 이미 벤리스타가 투여한 대상자 및 병원 이송 등으로 진단 시 이미 투여를 시작한 대상자도 포함된다.
제외 기준:
- 해당 없음
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 관찰 모델: 케이스 전용
- 시간 관점: 유망한
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
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Benlysta intravenous (IV)
Participants with systemic lupus erythematosus (SLE) received Benlysta via intravenous (IV) administration for 52 weeks as a part of their treatment regimen.
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Benlysta was administered
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Benlysta subcutaneous (SC)
Participants with SLE received Benlysta via subcutaneous (SC) administration for 52 weeks as a part of their treatment regimen.
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Benlysta was administered
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Benlysta switched from IV to SC or SC to IV
Participants with SLE received Benlysta for 52 weeks as a part of their treatment regimen, where initial administration was IV but switched to SC, or where the initial administration was SC but switched to IV during the study.
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Benlysta was administered
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Benlysta IV or SC (Initial route of administration unknown)
Participants with SLE received Benlysta via IV or SC administration for 52 weeks as a part of their treatment regimen.
It was unknown whether the initial administration was IV or SC for participants in this arm.
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Benlysta was administered
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Number of Participants With Adverse Drug Reactions (ADRs)
기간: From the start of the study intervention (Day 1) up to maximum of 3 years
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ADR is defined as a response to a drug which is noxious and unintended, and which occurred at doses normally used in human for the prophylaxis, diagnosis, or therapy of disease, or for the modifications of physiological function.
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From the start of the study intervention (Day 1) up to maximum of 3 years
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Number of Participants With Serious ADR of Events Defined as a Priority Study Matter
기간: From the start of the study intervention (Day 1) up to maximum of 3 years
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ADR is defined as a response to a drug which is noxious and unintended, and which occurred at doses normally used in human for the prophylaxis, diagnosis, or therapy of disease, or for the modifications of physiological function.
Following serious ADRs were considered as priority study matter: 1. Serious hypersensitivity, 2. Serious infections (including tuberculosis, pneumonia, pneumocystis pneumonia, sepsis, and opportunistic infection), 3. Reactivation of hepatitis B virus, 4. Progressive multifocal leukoencephalopathy, 5. Interstitial pneumonitis, 6. Malignant tumor, 7. Depression and events related to suicide/self-injury.
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From the start of the study intervention (Day 1) up to maximum of 3 years
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Change From Baseline in Safety of Estrogens in Lupus Erythematosus National Assessment Systemic Lupus Erythematosus Disease Activity Index (SELENA SLEDAI) Score at Week 24
기간: Baseline (Day 0) and Week 24
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The SELENA-SLEDAI score is a cumulative and weighted index for assessing systemic lupus erythematosus (SLE) disease activity in participants with SLE.
It consists of 24 disease descriptors related to signs and symptoms, laboratory tests, and physician's assessment across 9 organ systems.
Each descriptor is assigned a weighted score (8 descriptors with a weight of 8 each, 6 descriptors with a weight of 4 each, 7 descriptors with a weight of 2 each, and 3 descriptors with a weight of 1 each) which is added up if the descriptor is observed during a visit or within the preceding 10 days.
The total score ranges from 0 (no disease activity) to 105 (all 24 descriptors present simultaneously).
A higher score indicates a more significant degree of disease activity.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 24
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Change From Baseline in SELENA SLEDAI Score at Week 52
기간: Baseline (Day 0) and Week 52
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The SELENA-SLEDAI score is a cumulative and weighted index for assessing systemic lupus erythematosus (SLE) disease activity in participants with SLE.
It consists of 24 disease descriptors related to signs and symptoms, laboratory tests, and physician's assessment across 9 organ systems.
Each descriptor is assigned a weighted score (8 descriptors with a weight of 8 each, 6 descriptors with a weight of 4 each, 7 descriptors with a weight of 2 each, and 3 descriptors with a weight of 1 each) which is added up if the descriptor is observed during a visit or within the preceding 10 days.
The total score ranges from 0 (no disease activity) to 105 (all 24 descriptors present simultaneously).
A higher score indicates a more significant degree of disease activity.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 52
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Change From Baseline in Lupus Impact Tracker Score at Week 24
기간: Baseline (Day 0) and Week 24
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Lupus impact tracker is 10-item patient reported outcome tool to measure impact of systemic lupus erythematosus or its treatment on participants' daily lives.
Each answer for items is marked from 0 (none of the time) to 4 (all of the time) points.
Lower the lupus impact score, less impact lupus is having on life of participant.
Total score was derived by adding up scores of all 10 items.
Total score ranges from 0 (less impact on daily life) to 40 (greater impact on daily life).
Higher score indicates greater impact of lupus on quality of life.
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Baseline (Day 0) and Week 24
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Change From Baseline in Lupus Impact Tracker Score at Week 52
기간: Baseline (Day 0) and Week 52
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Lupus impact tracker is 10-item patient reported outcome tool to measure impact of systemic lupus erythematosus or its treatment on participants' daily lives.
Each answer for items is marked from 0 (none of the time) to 4 (all of the time) points.
Lower the lupus impact score, less impact lupus is having on life of participant.
Total score was derived by adding up scores of all 10 items.
Total score ranges from 0 (less impact on daily life) to 40 (greater impact on daily life).
Higher score indicates greater impact of lupus on quality of life.
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Baseline (Day 0) and Week 52
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Change From Baseline in Physician's Global Assessment (PGA) Score at Week 24
기간: Baseline (Day 0) and Week 24
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The PGA is used to assess the participant's current disease activity by investigator.
It was collected on a 10 centimeter (cm) visual analogue scale (VAS).
The score ranges from 0 (no activity) to 3 (severe activity).
Lower score means no disease activity, higher score means severe disease activity.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 24
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Change From Baseline in PGA Score at Week 52
기간: Baseline (Day 0) and Week 52
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The PGA is used to assess the participant's current disease activity by investigator.
It was collected on a 10 centimeter (cm) visual analogue scale (VAS).
The score ranges from 0 (no activity) to 3 (severe activity).
Lower score means no disease activity, higher score means severe disease activity.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 52
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 4
기간: Baseline (Day 0) and Week 4
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Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 4
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 8
기간: Baseline (Day 0) and Week 8
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Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 8
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 12
기간: Baseline (Day 0) and Week 12
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Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 12
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 16
기간: Baseline (Day 0) and Week 16
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Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 16
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 20
기간: Baseline (Day 0) and Week 20
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 20
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 24
기간: Baseline (Day 0) and Week 24
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Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 24
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 28
기간: Baseline (Day 0) and Week 28
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 28
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 32
기간: Baseline (Day 0) and Week 32
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 32
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 36
기간: Baseline (Day 0) and Week 36
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 36
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 40
기간: Baseline (Day 0) and Week 40
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 40
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 44
기간: Baseline (Day 0) and Week 44
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 44
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 48
기간: Baseline (Day 0) and Week 48
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
|
Baseline (Day 0) and Week 48
|
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Percent Change From Baseline in Mean Daily Steroid Dose at Week 52
기간: Baseline (Day 0) and Week 52
|
Mean daily steroid dose was calculated based on the prednisolone equivalent dose.
The average dose over the 7 days prior to and including the assessment date was used as mean daily steroid dose.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
Percent change from Baseline was calculated by dividing change from Baseline value by Baseline value and multiplying it by 100.
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Baseline (Day 0) and Week 52
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Number of Participants Who Achieved Lupus Low Disease Activity State (LLDAS) Response Criteria at Week 24
기간: At Week 24
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LLDAS was defined as a state which, if sustained, was associated with a low likelihood of adverse outcome, considering disease activity and medication safety.
The LLDAS response criteria were: (1) Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) less than equal to (<=)4 and no major active organ involvement (renal, central nervous system, cardiopulmonary, vasculitis, and pyrexia) and without hemolytic anemia or active gastrointestinal lesions; (2) no new signs or symptoms as compared to the last SELENA-SLEDAI assessment; (3) PGA score <=1 (33 millimeter); (4) corticosteroid dose <=7.5 milligram (mg)/day at time of assessment; and (5) use of the same immunosuppressant as compared with prior medication.
No unapproved immunosuppressant drugs like rituximab, anifrolumab, ustekinumab, or baricitinib were used as concomitant medications.
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At Week 24
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Number of Participants Who Achieved LLDAS Response Criteria at Week 52
기간: At Week 52
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LLDAS was defined as a state which, if sustained, was associated with a low likelihood of adverse outcome, considering disease activity and medication safety.
The LLDAS response criteria were: (1) Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) less than equal to (<=)4 and no major active organ involvement (renal, central nervous system, cardiopulmonary, vasculitis, and pyrexia) and without hemolytic anemia or active gastrointestinal lesions; (2) no new signs or symptoms as compared to the last SELENA-SLEDAI assessment; (3) PGA score <=1 (33 millimeter); (4) corticosteroid dose <=7.5 milligram (mg)/day at time of assessment; and (5) use of the same immunosuppressant as compared with prior medication.
No unapproved immunosuppressant drugs like rituximab, anifrolumab, ustekinumab, or baricitinib were used as concomitant medications.
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At Week 52
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Change From Baseline in Blood Levels of Anti-double-stranded Deoxyribonucleic Acid (Anti-dsDNA) Antibody at Week 24
기간: Baseline (Day 0) and Week 24
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Blood samples were collected for anti-dsDNA antibody biomarker analysis.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 24
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Change From Baseline in Blood Levels of Anti-dsDNA Antibody at Week 52
기간: Baseline (Day 0) and Week 52
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Blood samples were collected for anti-dsDNA antibody biomarker analysis.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 52
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Change From Baseline in Blood Levels of Complement Component-3 (C3) and Complement Component-4 (C4) at Week 24
기간: Baseline (Day 0) and Week 24
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Blood samples were collected from participants to assess C3 and C4 levels.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 24
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Change From Baseline in Blood Levels of Complement Component-3 (C3) and Complement Component-4 (C4) at Week 52
기간: Baseline (Day 0) and Week 52
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Blood samples were collected from participants to assess C3 and C4 levels.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 52
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Change From Baseline in Blood Levels of Complement Hemolytic Activity at 50% (CH50) at Week 24
기간: Baseline (Day 0) and Week 24
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Blood samples were collected from participants to assess CH50 concentrations.
CH50 is a blood test that measures the overall activity of the complement system, a group of proteins crucial for the immune system's function.
Low CH50 levels can be associated with certain infections.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 24
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Change From Baseline in Blood Levels of Complement Hemolytic Activity at 50% (CH50) at Week 52
기간: Baseline (Day 0) and Week 52
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Blood samples were collected from participants to assess CH50 concentrations.
CH50 is a blood test that measures the overall activity of the complement system, a group of proteins crucial for the immune system's function.
Low CH50 levels can be associated with certain infections.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 52
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Change From Baseline in Urine Protein/Creatinine Ratio at Week 24
기간: Baseline (Day 0) and Week 24
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Urine samples were collected from participants to assess Urine Protein/Creatinine Ratio.
It is a test that estimates how much protein is being excreted in urine, normalized to creatinine.
It's commonly used to assess kidney function and detect proteinuria.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 24
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Change From Baseline in Urine Protein/Creatinine Ratio at Week 52
기간: Baseline (Day 0) and Week 52
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Urine samples were collected from participants to assess Urine Protein/Creatinine Ratio.
It is a test that estimates how much protein is being excreted in urine, normalized to creatinine.
It's commonly used to assess kidney function and detect proteinuria.
Baseline was considered as Day 0 of the study.
Change from Baseline was defined as value at the indicated time point minus Baseline value.
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Baseline (Day 0) and Week 52
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
스폰서
수사관
- 연구 책임자: GSK Clinical Trials, GlaxoSmithKline
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
2018년 1월 15일
기본 완료 (실제)
2025년 7월 31일
연구 완료 (실제)
2025년 7월 31일
연구 등록 날짜
최초 제출
2017년 12월 6일
QC 기준을 충족하는 최초 제출
2017년 12월 6일
처음 게시됨 (실제)
2017년 12월 12일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 5월 18일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 4월 24일
마지막으로 확인됨
2026년 4월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 207735
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
아니요
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미국 FDA 규제 의약품 연구
아니
미국 FDA 규제 기기 제품 연구
아니
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
전신성 홍반성 루푸스에 대한 임상 시험
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Union Hospital, Tongji Medical College, Huazhong...아직 모집하지 않음전신 홍반성 루푸스(Systemic Lupus Erythematosus, SLE)중국
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Istanbul Galata UniversityThe Scientific and Technological Research Council of Turkey아직 모집하지 않음전신 홍반성 루푸스(Systemic Lupus Erythematosus, SLE)터키 (Türkiye)
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Tongji Hospital아직 모집하지 않음전신 홍반성 루푸스(Systemic Lupus Erythematosus, SLE)중국
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University of California, San Francisco완전한
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Union Hospital, Tongji Medical College, Huazhong...Everest Medicines (China) Co.,Ltd.모병경피증 | 전신 홍반성 루푸스(Systemic Lupus Erythematosus, SLE) | 중증근무력증(MG)중국
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University of the West of EnglandAlder Hey Children's NHS Foundation Trust; Bristol Royal Hospital for Children; Glasgow Royal...모병
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West China Hospital알려지지 않은
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Chitwan Medical College완전한Neplaese Lupus Nephritis 환자에서 Mycophenolate Mofetil과 Cyclophosphamide의 효과 비교
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Aga Khan University알려지지 않은뇌병증, 간 | 간뇌 뇌병증 | Portal-Systemic Encephalopathy | 뇌병증, 간뇌파키스탄
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University Hospital Freiburg모병간경화 | 문맥 고혈압 | 문맥 혈전증 | 비간경변 문맥 고혈압 | 버드 키아리 증후군 | Portal Systemic Shunt독일
Benlysta에 대한 임상 시험
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GlaxoSmithKline모병경피증, 전신 | 전신 경화증 관련 간질성 폐질환미국, 호주, 프랑스, 스페인, 그리스, 이스라엘, 일본, 영국, 핀란드, 중국, 아르헨티나, 이탈리아, 브라질, 덴마크, 벨기에, 멕시코, 독일, 대한민국
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Human Genome Sciences Inc.GlaxoSmithKline완전한전신성 홍반성 루푸스홍콩, 대만, 대한민국, 인도, 칠레, 아르헨티나, 필리핀 제도, 콜롬비아, 브라질, 루마니아, 호주, 페루, 러시아 연방