- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07609706
A Study of the Combination of Belantamab Mafodotin, Bortezomib, and Dexamethasone (BVd) in Participants With Multiple Myeloma and Moderate Hepatic Impairment
2026년 5월 20일 업데이트: GlaxoSmithKline
A Phase 1 Study to Evaluate the Pharmacokinetics and Safety of the Combination of Belantamab Mafodotin, Bortezomib, and Dexamethasone (BVd) in Participants With Multiple Myeloma and Moderate Hepatic Impairment
The goal of the clinical trial is to collect safety data and information on how the body processes BVd in people with multiple myeloma (MM) who have moderate liver problems, compared with similar participants who have normal liver function.
It also compares how liver problems affect the body's handling of belantamab mafodotin and uses the results to help set safe and appropriate dosing guidance for MM participants with moderate liver problems.
연구 개요
연구 유형
중재적
등록 (추정된)
20
단계
- 1단계
확장된 액세스
사용 가능 임상시험 외.
확장 액세스 기록을 참조하세요.
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: US GSK Clinical Trials Call Center
- 전화번호: 877-379-3718
- 이메일: GSKClinicalSupportHD@gsk.com
연구 연락처 백업
- 이름: EU GSK Clinical Trials Call Center
- 전화번호: +44 (0) 20 89904466
- 이메일: GSKClinicalSupportHD@gsk.com
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
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
아니
설명
Inclusion Criteria:
- Is at least 18 years of age or the legal age of consent in the jurisdiction in which the study is taking place at the time of signing the informed consent form (ICF).
- Has histologically or cytologically confirmed diagnosis of MM, as defined by the International Myeloma Working Group (IMWG).
- Previously treated with at least 1 prior line of MM therapy and must have documented disease progression during or after their most recent therapy.
Has at least 1 aspect of measurable disease, defined as at least 1 of the following:
- Urine M-protein excretion ≥200 milligram (mg)/24 hours (≥0.2 gram [g]/24 hours)
- Serum M-protein concentration ≥0.5 g/ deciliter (dL) (≥5.0 g/L)
- Serum Free light chain (FLC) assay: involved FLC level ≥10 mg/dL (≥100 mg/L) and an abnormal serum FLC ratio (<0.26 or >1.65).
- Plasmacytoma measurable as per IMWG criteria
- Bone Marrow infiltration by plasma cells >30%
- For those participants with a history of autologous stem cell transplant, they are eligible for study participation provided the following eligibility criteria are met: transplant was >100 days prior to study enrollment; no active infection(s); participant meets the remainder of the eligibility criteria
- All prior treatment-related toxicities (defined by National Cancer Institute Common terminology criteria for adverse events [NCI-CTCAE] v5.0) must be Grade ≤1 at the time of treatment assignment, except for alopecia (any grade), neuropathy (Grade ≤2), or endocrinopathy managed with replacement therapy (any grade).
- Is willing to use adequate contraception male and female participants.
- Female participants are eligible to participate if they are not pregnant or breastfeeding and meet additional requirements.
- Is capable of giving signed informed consent including compliance with the requirements and restrictions listed in the ICF and protocol.
- Has adequate organ function for hematological and renal function tests.
- Has specific hepatic function ranges for serum bilirubin and AST for Group 1 and Group 2.
- Participants in Group 1 (normal hepatic function) will only be enrolled if they match a participant in Group 2 (moderate hepatic impairment). Each Group 1/Group 2 pair will be matched based on the Group 2 participant's baseline body weight (±20%).
- Participants with a history of Hepatitis B virus (HBV) and/or Hepatitis C virus (HCV) and Human immunodeficiency virus (HIV) exposure are eligible under specific conditions
Exclusion Criteria:
- Has an active plasma cell leukemia at the time of screening, symptomatic amyloidosis, active POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes), or Waldenström macroglobulinemia.
- Has a previous or concurrent invasive malignancy other than MM, except for any other disease from which the participant must be considered medically stable for at least 1 year; or the participant must not be receiving active therapy, other than hormonal therapy for this disease.
- Known immediate or delayed hypersensitivity reaction or idiosyncratic reaction to drugs chemically related to belantamab mafodotin, or any of the components of the study treatment.
- Has evidence of active mucosal or internal bleeding.
- Has a systemic active infection requiring treatment.
- Has had any major surgery (other than bone-stabilizing surgery) within 28 days prior to the first dose of study treatment.
- Has current corneal epithelial disease except for mild superficial keratopathy.
- Has any serious and/or unstable medical or psychiatric disorder or other condition(s) (including laboratory assessment abnormalities) that could interfere with the participant's safety, obtainment of informed consent, or compliance to the study procedures.
- Has any history of prior allogenic stem cell transplant. Participants who have undergone syngeneic transplant will be allowed only if no history of or no currently active graft versus host disease.
- Has received prior belantamab mafodotin therapy if given within the last 90 days.
- Has received treatment with an investigational agent within 14 days or 5 half-lives, whichever is shorter, preceding the first dose of study drug. This includes prior treatment with a monoclonal antibody and any other B-cell maturation antigen (BCMA) targeting therapy. The only exception is emergency use of a short course of systemic corticosteroids (equivalent to, or less than: dexamethasone 40 mg/day for a maximum of 4 days) before treatment.
- Has received treatment with an inhibitor of Organic anion transporting polypeptide (OATP)1B1 or OATP1B3 within 14 days, preceding the first dose of study drug.
- Has received plasmapheresis within 7 days prior to the first dose of study treatment. Screening laboratory values must be performed after last plasmapheresis.
- Has received any live vaccine within 30 days of enrollment. Vaccination against COVID-19 using vaccines that are authorized via the appropriate regulatory mechanisms (e.g., Conditional Marketing Authorization, or Marketing Authorization Application) are not exclusionary.
Has a known HIV infection, unless the participant meets all of the following criteria:
- Established Anti-retroviral therapy (ART) for at least 4 weeks and HIV viral load <400 copies/milliliter (mL) prior to first dose.
- Has CD4+ T-cell count values ≥350 cells/L
- No history of acquired immunodeficiency syndrome (AIDS)-defining opportunistic infections within the last 12 months.
- Is pregnant, plans to become pregnant, or is breastfeeding.
- Has Gilbert's syndrome.
- Has current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal/gastric varices, or persistent jaundice in the last 14 days prior to the first dose.
- Has documented presence of Hepatitis B surface antigen (HBsAg) and/or Hepatitis B core antibody (HBcAb) at screening or within 3 months prior to the first dose of study intervention. Participants with hepatitis B will be excluded unless the specific protocol criteria are met.
- Has a positive Hepatitis C virus (HCV) antibody test result at screening or within 3 months prior to the first dose of study intervention unless HCV ribonucleic acid (RNA) is negative, indicating past resolved HCV infection, including participants who have undergone curative treatment, unless specific protocol criteria are met
- Has a positive HCV RNA test result at screening or within 3 months prior to the first dose of study intervention.
Evidence of cardiovascular risk including any of the following:
- Evidence of current clinically significant untreated arrhythmias, including clinically significant electrocardiogram (ECG) abnormalities including second degree (Mobitz Type II) or third degree atrioventricular block.
- History of myocardial infarction, acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting or bypass grafting within 3 months of Screening.
- Class III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system.
- Uncontrolled hypertension.
- Has QT interval corrected (QTc) >450 milliseconds (msec) or QTc >480 msec for participants with bundle branch block
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: 정상적인 간 기능
|
Belantamab mafodotin이 투여됩니다.
덱사메타손이 투여됩니다.
보르테조밥이 투여됩니다.
|
|
실험적: 중등도 간 장애
|
Belantamab mafodotin이 투여됩니다.
덱사메타손이 투여됩니다.
보르테조밥이 투여됩니다.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Area under the plasma concentration-time curve from time 0 to the end of the dosing interval (AUC 0-tau) of belantamab mafodotin antibody drug conjugate (ADC)
기간: Up to 3 weeks
|
Up to 3 weeks
|
|
Maximum observed plasma concentration (Cmax) of belantamab mafodotin ADC
기간: Up to 3 weeks
|
Up to 3 weeks
|
|
Concentration at end of infusion (C-EOI) of belantamab mafodotin ADC
기간: Up to 104 weeks
|
Up to 104 weeks
|
|
Drug concentration reached prior to next dose (Ctrough) of belantamab mafodotin ADC
기간: Up to 104 weeks
|
Up to 104 weeks
|
|
Time to reach Cmax (Tmax) of belantamab mafodotin ADC
기간: Up to 3 weeks
|
Up to 3 weeks
|
|
Area under the plasma concentration-time curve from time 0 to 168 hours (AUC 0-168h) of microtubule inhibitor released from belantamab mafodotin (cys-mcMMAF)
기간: Up to 168 hours
|
Up to 168 hours
|
|
Area under the plasma concentration-time curve from time 0 to 240 hours (AUC 0-240h) of cys-mcMMAF
기간: Up to 240 hours
|
Up to 240 hours
|
|
Cmax of cys-mcMMAF
기간: Up to 3 weeks
|
Up to 3 weeks
|
|
Tmax of cys-mcMMAF
기간: Up to 3 weeks
|
Up to 3 weeks
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Number of participants with adverse events (AEs) and serious AEs by severity
기간: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Number of participants with AEs leading to dose modifications or study intervention discontinuation
기간: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Number of participants with changes in visual acuity (VA) and corneal findings by severity as assessed by Keratopathy Visual Acuity scale (KVA) scale
기간: Up to 252 weeks
|
The Keratopathy-Visual Acuity (KVA) scale is a 0-4 grading system used to assess the severity of keratopathy and its impact on visual acuity.
Higher grades reflect increasing severity of corneal findings and visual acuity loss.
|
Up to 252 weeks
|
|
Number of participants with ocular AEs by severity as assessed by Common terminology criteria for adverse events (CTCAE)
기간: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Number of participants with thrombocytopenic events by severity
기간: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Change from baseline in clinical laboratory parameter: serum bilirubin (milligrams per decilitre[mg/dl])
기간: Baseline (Day 1) and up to 252 weeks
|
Baseline (Day 1) and up to 252 weeks
|
|
|
Change from baseline in clinical laboratory parameter: AST and ALT (International Units per litre [IU/L])
기간: Baseline (Day 1) and up to 252 weeks
|
Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) will be analysed.
Both parameters have same unit of measure.
|
Baseline (Day 1) and up to 252 weeks
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
스폰서
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 (추정된)
2026년 10월 23일
기본 완료 (추정된)
2031년 8월 22일
연구 완료 (추정된)
2031년 8월 22일
연구 등록 날짜
최초 제출
2026년 5월 20일
QC 기준을 충족하는 최초 제출
2026년 5월 20일
처음 게시됨 (실제)
2026년 5월 27일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 5월 27일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 5월 20일
마지막으로 확인됨
2026년 5월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 308247
- 2026-526725-18-00 (씨티스)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
아니요
IPD 계획 설명
GSK will assess requests from qualified researchers for anonymized individual patient-level data and related study documents.
Data sharing is subject to certain criteria, conditions, and exceptions.
For further information, refer to https://www.gsk-studyregister.com/gsk-patient-level-data-sharing-july2025.pdf
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
예
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. .
다발성 골수종에 대한 임상 시험
-
Sanko University완전한MULTİPLE SCLEROSİS | BALANCE | 유효성 | 신뢰도터키 (Türkiye)
-
University Hospital, Montpellier종료됨제1형 당뇨병 | Basal-bolus multiple-dily 인슐린 주사 | 인슐린 펌프(CSII)프랑스
벨란타맙 마포도틴에 대한 임상 시험
-
GlaxoSmithKline빼는
-
University of PennsylvaniaGlaxoSmithKline모집하지 않고 적극적으로
-
Cristiana Costa Chase, DO아직 모집하지 않음
-
M.D. Anderson Cancer Center모병
-
Stichting European Myeloma NetworkGlaxoSmithKline완전한AL 아밀로이드증네덜란드, 독일, 그리스, 프랑스, 이탈리아, 영국
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GlaxoSmithKline모집하지 않고 적극적으로다발성 골수종미국, 호주, 스웨덴, 독일, 프랑스, 캐나다, 네덜란드, 스페인
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Jacob Soumerai, MDGlaxoSmithKline종료됨재발성 형질모세포성 림프종 | 난치성 형질모세포성 림프종 | 역형성 림프종 키나아제 양성 대형 B세포 림프종미국
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GlaxoSmithKline빼는
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GlaxoSmithKline완전한다발성 골수종캐나다, 미국, 대만, 폴란드, 태국, 이탈리아, 아일랜드, 멕시코, 영국, 호주, 스페인, 스위스, 그리스, 아르헨티나, 브라질, 독일, 프랑스, 대한민국