전이성 흑색종 및 두경부 편평 세포 암종 환자에서 GB1211 및 펨브롤리주맙 대 펨브롤리주맙 및 위약
전이성 흑색종 및 두경부 편평 세포 암종 환자를 대상으로 갈렉틴-3 억제제(GB1211) 및 펨브롤리주맙 대 펨브롤리주맙 및 위약의 무작위 이중맹검 위약 대조 제2상 연구
The purpose of this study is to determine the objective response of GB1211 and pembrolizumab versus pembrolizumab and placebo in patients with advance metastatic melanoma or head and neck squamous cell carcinoma.
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
상세 설명
Eligible patients will be registered, stratified by diagnosis (melanoma versus oral, head and neck (OHN) cancer), and the number of prior systemic therapies, and randomized to receive either GB1211 + pembrolizumab or pembrolizumab + placebo.
연구 유형
연구 유형
등록 (실제)
등록
단계
단계
- 2 단계
연락처 및 위치
연구 장소
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Oregon
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Portland, Oregon, 미국, 97213
- Providence Portland Medical Center
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Patients with unresectable or metastatic melanoma including unknown primary or mucosal melanomas. Histological confirmation of melanoma will be required by previous biopsy or cytology. Patients with recurrent or metastatic head and neck squamous cell carcinoma (HNSCC) with disease progression during or after platinum-containing chemotherapy are eligible. PD-L1 testing is not needed for OHN cancers.
- Patients who have received anti-PD1 or anti-PD-L1 in the past are eligible if it has been at least 6 months since the last anti-PD-1 or PD-L1 dose, they meet all other eligibility criteria and progression of malignancy has been documented on imaging. Progression for this patient subset is defined as the appearance of one or more new metastatic sites, or a 5% or greater increase in the sum of diameter of target lesions or an unequivocal increase in non-target site. Treatment naïve melanoma patients are eligible.
- Patients must be ≥ 18 years of age.
- ECOG performance status of 0-2.
- Women of childbearing potential must have a serum or urine pregnancy test performed within 72 hours prior to the start of protocol treatment. The results of this test must be negative in order for the patient to be eligible. In addition, women of childbearing potential as well as male patients must agree to take appropriate precautions to avoid pregnancy.
- No active bleeding.
- Anticipated lifespan greater than 12 weeks.
- Patients must sign a study-specific consent document.
Exclusion Criteria:
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Patients who have previously received a galectin antagonist.
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Patients with active autoimmune disease except for autoimmune thyroiditis or vitiligo.
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Patients with history of autoimmune colitis.
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Patients with untreated brain metastases. Patients with treated brain metastases who demonstrate control of brain metastases with follow-up imaging 4 or more weeks after initial therapy are eligible.
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Patients requiring other systemic oncologic therapy, including experimental therapies.
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Patients who have received anti-cancer treatment within 3 weeks or 5 half-lives before first study drug dose.
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Patients with Child-Pugh C hepatic impairment.
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Patients with active infection requiring antibiotics.
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Pregnant or lactating women, as treatment involves unforeseeable risks to the embryo or fetus.
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Need for steroids at greater than physiologic replacement doses. Inhaled corticosteroids are acceptable.
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Laboratory exclusions (to be performed within 28 days of enrollment):
- WBC < 3.0 x 109/L
- Hgb < 9.0 g/dL
- AST or ALT > 1.5 times ULN
- Total bilirubin > 1.9 g/dL, unless due to Gilbert's Syndrome. If Gilbert's Syndrome is present by clinical history, then direct bilirubin must by < 3.0 g/dl.
- Active or known history of HIV
- Active or known history of Hepatitis B
- Active or known history of Hepatitis C
- Platelet counts < 100 x 10E9 / L (100,000/ μL) without transfusion
- INR > 1.5x ULN
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Inability to give informed consent and comply with the protocol. Patients must be judged able to understand fully the investigational nature of the study and the risks associated with the therapy.
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Any medical condition that in the opinion of the Principal Investigator would compromise the safety or conduct of the study procedures.
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Unresolved immune-mediated pneumonitis, diarrhea, elevation of hepatocellular enzymes or other toxicities requiring greater than physiological replacement doses of steroids.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
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실험적: GB1211 + Pembrolizumab
GB1211 will be administered orally twice a day at 400mg in combination with standard pembrolizumab treatment. |
Administered orally twice daily at 100mg. Administered at a fixed dose of 200 mg every 3 weeks intravenously.
다른 이름들:
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위약 비교기: Pembrolizumab Monotherapy
Placebo will have the same appearance as GB1211 and administered orally twice a day in combination with standard pembrolizumab treatment. |
Administered at a fixed dose of 200 mg every 3 weeks intravenously.
다른 이름들:
Administered orally twice daily at 100mg. |
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Overall response rate based on disease imaging
기간: From the date of randomization until the date of first documented progression, assessed up to 63 weeks.
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Determine the response of Gal-3 inhibitor and pembrolizumab versus pembrolizumab monotherapy (plus placebo) in patients with metastatic melanoma or head and neck squamous cell carcinoma (HNSCC). |
From the date of randomization until the date of first documented progression, assessed up to 63 weeks.
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2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Evaluation of GAL-3 Expression
기간: Screening and Day 68
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Compare Gal-3 expression in paired biopsies after GB1211 + pembrolizumab or pembrolizumab monotherapy |
Screening and Day 68
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Evaluation of Predictive Biomarker
기간: Day 85
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Characterize myeloid-derived suppressor cells (MDSC) expression over time as a predictive biomarker of response after GB1211 + pembrolizumab or pembrolizumab monotherapy |
Day 85
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Frequency of Immune-mediated Adverse Events
기간: From the time of informed consent to week 63
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Compare the frequency of immune-mediated adverse events after GB1211 + pembrolizumab versus pembrolizumab + placebo |
From the time of informed consent to week 63
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Evaluation of Antiviral Immunity
기간: Day 85
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Assess the biological activity of GB1211 + pembrolizumab and in comparison to pembrolizumab monotherapy by measuring CD4+T cells with a memory phenotype (CD3+CD4+Ki67+CD25+FoxP3-CCR7-CD45RA-CD27+CD28+/-). |
Day 85
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Evaluation of Antiviral Immunity
기간: Day 85
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Assess the biological activity of GB1211 + pembrolizumab and in comparison to pembrolizumab monotherapy by measuring CD8+ T cells with effector phenotype (CD3+CD8+CD28-CD95+). |
Day 85
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Evaluation of Antiviral Immunity
기간: Day 85
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Assess the biological activity of GB1211 + pembrolizumab and in comparison to pembrolizumab monotherapy by measuring tumor-specific T cells using autologous and/or HLA-matched tumor when available. |
Day 85
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공동 작업자 및 조사자
협력자
협력자
수사관
수사관
- 수석 연구원: Brendan D. Curti, MD, Providence Health & Services
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- 2023000353
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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