- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07619313
AB801 in Combination With Chemotherapy and Immunotherapy for the Treatment of Patients With Borderline Resectable, Locally Advanced or Metastatic Cholangiocarcinoma or Pancreatic Cancer
A Phase 1/1b Trial of AB801 in Combination With Chemotherapy and PD-1/PD-L1 Blockade in Patients With Cholangiocarcinoma or Pancreatic Adenocarcinoma
연구 개요
상태
정황
상세 설명
PRIMARY OBJECTIVE:
I. Assess safety and tolerability of ligritinib (AB801) in combination with chemotherapy and immunotherapy in patients with cholangiocarcinoma and pancreatic adenocarcinoma.
SECONDARY OBJECTIVES:
I. Objective response rate. II. Progression free survival. III. Duration of response. IV. Proportion of patients taken to curative intent surgery after neoadjuvant therapy.
EXPLORATORY OBJECTIVES:
I. To evaluate the effect on AXL expression by comparing pre-treatment core biopsies with post-therapy operative specimens or biopsies taken at time of progression.
II. To evaluate the effects of study treatment on tumor microenvironment by comparing pre-treatment core biopsies with operative specimens or biopsies taken at time of progression via multiple modalities including immunohistochemistry (IHC), cytometry by time-of-flight (CyTOF), ribonucleic acid sequencing (RNA Seq)/spatial transcriptomics.
III. To assess for changes in peripheral blood throughout treatment including but not limited to soluble AXL, immune cell populations and change in systemic cytokines.
IV. To explore changes in gene alterations via whole exome sequencing.
OUTLINE: This is a dose-escalation study of AB801 followed by a dose-expansion study. Patients are assigned to 1 of 2 cohorts.
COHORT I: Patients with cholangiocarcinoma receive AB801 orally (PO) once daily (QD), gemcitabine and cisplatin intravenously (IV) over 30 minutes on days 1 and 8 and durvalumab IV over 60 minutes on day 1 of each cycle. Cycles repeat every 21 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
COHORT II: Patients with pancreatic cancer receive AB801 PO QD and zimberelimab IV over 60 minutes on day 1 of each cycle. Patients receive oxaliplatin IV over 120 minutes, leucovorin IV, and irinotecan IV on days 1 and 15 of each cycle and fluorouracil IV over 46 hours on days 1 and 15 of each cycle. Cycles repeat every 28 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
All patients undergo computed tomography (CT) or magnetic resonance imaging (MRI) throughout the trial as well as tissue biopsy on trial.
After completion of study treatment, patients are followed up at 30 and 90 days and then every 3 months.
연구 유형
등록 (추정된)
단계
- 1단계
연락처 및 위치
연구 장소
-
-
California
-
Los Angeles, California, 미국, 90095
- 모병
- UCLA / Jonsson Comprehensive Cancer Center
-
수석 연구원:
- Lee S. Rosen, MD
-
연락하다:
- Christopher Lim
- 전화번호: 310-633-8400
- 이메일: ChristopherLim@mednet.ucla.edu
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Male or female ≥ 18 years of age and willing and able to provide informed consent
Previously untreated cytologically or histologically confirmed, at least one measurable lesion via Response Evaluation Criteria in Solid Tumors (RECIST 1.1) of cholangiocarcinoma or pancreatic adenocarcinoma meeting following criteria:
Cholangiocarcinoma
- Borderline resectable/locally advanced cholangiocarcinoma: to be defined as unresectable disease on evaluation by a hepatobiliary multi-disciplinary tumor board/surgeon based on tumor size/location, vascular involvement, and absence of extrahepatic metastasis.
- Metastatic cholangiocarcinoma: Patients with metastatic cholangiocarcinoma patient who have not received prior systemic therapy
Pancreatic adenocarcinoma
Borderline resectable pancreatic adenocarcinoma: There are multiple definitions of borderline resectable pancreatic ductal adenocarcinoma (PDAC). For the purposes of this study, borderline resectable disease will be identified per the National Comprehensive Cancer Network (NCCN) criteria. Per this definition, borderline resectable PDAC is defined as the presence of any one or more of the following on CT:
- An interface between the tumor and superior mesenteric artery (SMA) or celiac axis (CA) measuring < 180º of the circumference of the vessel wall.
- An interface between the tumor with the common hepatic artery without extension into the celiac axis or hepatic artery bifurcation allowing for safe and complete resection and reconstruction.
- An interface between the primary tumor and the superior mesenteric vein or portal vein (SMV-PV) measuring ≥ 180° of the circumference of the vessel wall
- Short-segment occlusion of the SMV-PV with normal vein above and below the level of obstruction that is amenable to resection and venous reconstruction
- An interface between the primary tumor and the inferior vena cava (IVC)
Locally advanced pancreatic adenocarcinoma: Multiple guidelines defining locally advanced PDAC have been developed. For the purposes of this study, locally advanced PDAC cases will be identified per the definition developed by the NCCN. Per this definition, locally advanced PDAC is defined as presence of any one or more of the following on CT:
- Interface between the tumor and SMA or CV measuring > 180º of the circumference of the vessel wall or solid tumor contact with the CA and aortic involvement.
- Occlusion of the SMV-PV that is not amenable to resection and venous reconstruction
- Metastatic pancreatic adenocarcinoma: Patients with metastatic pancreatic adenocarcinoma who have not received prior systemic therapy
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- Absolute neutrophil count (ANC) ≥ 1.5x10^9/L
- Platelets ≥ 100x10^9/L
- Hemoglobin ≥ 9 g/dL
- Creatinine clearance (Ccr) ≥ 50 mL/min (as calculated by Modified Cockcroft-Gault formula)
- Serum total bilirubin ≤ 2x upper limit of normal (ULN) or < 3x ULN if Gilbert's syndrome
- Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamic-pyruvic transaminase [SGPT]) ≤ 2.5 X ULN; < 5x ULN in patients with liver metastases
- Women with no childbearing potential because of surgery or who are at least 1 year postmenopausal (ie, 12 months post last menstrual period) or with menopause confirmed by follicle-stimulating hormone testing, OR
- Women of childbearing potential (defined as any female who has experienced menarche and is not permanently sterile or post-menopausal) must use an effective nonhormonal method of contraception (intrauterine device or intrauterine system; condom or occlusive cap [diaphragm or cervical or vault caps] with spermicidal foam or gel or film or cream or suppository; or vasectomized male partner if he is the sole partner of that participant) or practice true abstinence for the duration of the study and for up to 14 months after the last systemic treatment
- Male participants must use an effective method of contraception (condom or occlusive cap [diaphragm or cervical or vault caps] with spermicidal foam or gel or film or cream or suppository; or vasectomy) or practice true abstinence as defined throughout the study and for up to 11 months after the systemic treatment
- Immunosuppressive doses of systemic medications, such as corticosteroids or absorbed topical corticosteroids (doses > 10 mg/day prednisone or equivalent) must be discontinued at least 2 weeks (14 days) before study treatment administration. Physiologic doses of corticosteroids (≤ 10 mg/day of prednisone or its equivalent) or short pulses of corticosteroids (≤ 3 days) may be permitted
- Products with known potential to prolong the corrected QT (QTc) interval should be avoided when possible. When able will replace non-prolonging QTc acting drug when available and if medically necessary
- Major surgery as defined by the Investigator must be completed at least 4 weeks before study treatment administration. Participants should have recovered from the surgical procedure prior to the first dose being administered
- Adequate baseline tumor tissue sample for correlative studies
Exclusion Criteria:
- Previous treatment with any of planned study drugs in cholangiocarcinoma, though patients with one cycle of gemcitabine/cisplatin/durvalumab will be considered eligible
- Previous treatment with any of planned study drugs in pancreatic adenocarcinoma, though patients with one cycle of FOLFIRINOX will be considered eligible
- Peripheral neuropathy > grade 2
- Known status of HIV which is not well-controlled (CD4 < 300) at the time of study eligibility. Patients with controlled and treated HIV/hepatitis C virus (HCV) and an undetectable viral load are allowed
Untreated hepatitis B infection; Patient has known active hepatitis B virus (HBV) or hepatitis C virus (HCV), or human immunodeficiency virus (HIV) infection (testing is not mandatory, unless known active or known history of infection or required by local regulation):
- Participants with resolved or treated HCV (ie, HCV antibody positive but undetectable HCV ribonucleic acid [RNA]) will not be excluded from this study
Underlying medical conditions that, in the Investigator's opinion, will make the administration of investigational product (IP)(s) hazardous, including but not limited to:
- Interstitial lung disease, including history of interstitial lung disease or non-infectious pneumonitis
- Active viral, bacterial, or fungal infections requiring parenteral treatment within 14 days of the initiation of the IP,
- Active infection or antibiotics within 48 hours prior to study screening;
- A condition or unresolved adverse event (AE) from a prior investigational drug that may obscure the interpretation of toxicity determination or AEs,
- History of prior solid-organ transplantation
- Any history of malignancy less than 5 years prior to the time of study eligibility (Patients with history of skin cancers excluding melanoma and cancers with a very low risk of recurrence i.e., low grade prostate cancer, thyroid cancer and low risk cervical cancer will be eligible for participation)
- Serious medical comorbidities such as New York Heart Association Class III/IV cardiac disease, uncontrolled cardiac arrhythmias, myocardial infarction over the past 12 months
- Known family history or personal history of long QTc syndrome or previous drug-induced QTc prolongation of at least grade 3 (QTc > 500 ms)
- Screening 12-lead electrocardiogram (ECG), in triplicate, with a measurable QTc interval of > 450ms
- Known, existing uncontrolled coagulopathy. Patients who have had a venous thromboembolic event (e.g., pulmonary embolism or deep vein thrombosis) requiring anticoagulation are eligible IF: they are appropriately anticoagulated and have not had a grade 2 or greater bleeding episode in the 3 weeks before day 1
- Known pregnancy, nursing women or positive pregnancy test. Requirement for women of childbearing potential (WOCBP): Negative serum pregnancy test at screening and serum or urine prior to dosing on cycle 1 day 1, within 24 hours prior to the start of treatment (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]). WOCBP must also have a negative serum or urine pregnancy test every 3 weeks, within 24 hours prior to the start of treatment
- Any condition (concurrent disease, infection, or comorbidity) that interferes with ability to participate in the study, causes undue risk, or complicates the interpretation of safety data, in the opinion of the investigator
- History of trauma or major surgery within 28 days prior to the first dose of IP
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
Any active or documented history of autoimmune disease, including but not limited to inflammatory bowel disease, celiac disease, Wegner syndrome, Hashimoto syndrome, systemic lupus erythematosus, scleroderma, sarcoidosis, or autoimmune hepatitis, within 3 years of the first dose of study treatment, except for the following:
- Type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders such as vitiligo, or alopecia not requiring systemic therapy, or conditions not expected to recur in the absence of an external trigger.
- Endocrinopathies where the participant is stable on hormone replacement therapy
- History of Hashimoto syndrome within 3 years of the first of study treatment that resolved to hypothyroidism alone
공부 계획
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: Cohort I (AB801, gemcitabine, cisplatin, durvalumab)
Patients with cholangiocarcinoma receive AB801 PO QD, gemcitabine and cisplatin IV over 30 minutes on days 1 and 8 and durvalumab IV over 60 minutes on day 1 of each cycle.
Cycles repeat every 21 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
Patients undergo CT or MRI throughout the trial as well as tissue biopsy on trial.
|
MRI를 받다
다른 이름들:
주어진 IV
다른 이름들:
주어진 IV
다른 이름들:
CT를 받다
다른 이름들:
주어진 IV
다른 이름들:
조직 생검을받습니다
다른 이름들:
Given PO
다른 이름들:
|
|
실험적: Cohort II (AB801, zimberelimab, FOLFIRINOX)
Patients with pancreatic cancer receive AB801 PO QD and zimberelimab IV over 60 minutes on day 1 of each cycle.
Patients receive oxaliplatin IV over 120 minutes, leucovorin IV, and irinotecan IV on days 1 and 15 of each cycle and fluorouracil IV over 46 hours on days 1 and 15 of each cycle.
Cycles repeat every 28 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
Patients undergo CT or MRI throughout the trial as well as tissue biopsy on trial.
|
MRI를 받다
다른 이름들:
CT를 받다
다른 이름들:
주어진 IV
다른 이름들:
주어진 IV
다른 이름들:
주어진 IV
다른 이름들:
주어진 IV
조직 생검을받습니다
다른 이름들:
Given PO
다른 이름들:
Give IV
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Incidence of dose limiting toxicities
기간: During first cycle of the dose escalation phase (cycle length = 21 days for cohort I and 28 days for cohort II)
|
Overall exposure to study drug, the numbers of participants completing each cycle, and the dose intensity will be summarized using descriptive statistics.
The number of participants with any dose adjustment will be presented for entire treatment period as well as for each cycle.
The number of participants with dose reductions, dose delays, or dose omissions will also be summarized, as will the reasons for dose adjustments.
Adverse events and serious adverse events will be reported using Common Terminology Criteria for Adverse Events version 5 terminology and severity.
|
During first cycle of the dose escalation phase (cycle length = 21 days for cohort I and 28 days for cohort II)
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Overall response rate (ORR)
기간: Up to 2 years
|
Will be defined as proportion of patients with complete response (CR) or partial response (PR) at time of data analysis.
ORR and their corresponding exact 2-sided 95% confidence interval will be calculated.
|
Up to 2 years
|
|
Overall survival
기간: Up to 2 years
|
Will be estimated using Kaplan-Meier method.
|
Up to 2 years
|
|
Proportion of patients take to curative surgery
기간: Up to 2 years
|
Will be analyzed using descriptive statistics.
|
Up to 2 years
|
|
Duration of response
기간: up to 2 years
|
Will be summarized and plotted over time by Kaplan-Meier method.
Time from the first documentation of CR or PR to the date of first documentation of disease progression or death (whichever occurs first).
|
up to 2 years
|
|
Progression-free survival
기간: up to 2 years
|
Will be estimated using Kaplan-Meier method.
Time from first study dose date to the date of first documentation of disease progression or death (whichever comes first)
|
up to 2 years
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Lee S Rosen, UCLA / Jonsson Comprehensive Cancer Center
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
- 내분비계 질환
- 부위별 신생물
- 신생물
- 조직학적 유형에 따른 신생물
- 소화계 신생물
- 소화기계 질환
- 내분비샘 신생물
- 췌장 질환
- 신생물, 선상 및 상피
- 선암종
- 암종
- 췌장 신생물
- 담관암
- 아미노산, 펩티드 및 단백질
- 단백질
- 황 화합물
- 유기 화학 물질
- 이종 사이 클릭 화합물, 1- 링
- 이종 사이 클릭 화합물
- 이종 사이 클릭 화합물, 2- 링
- 이종 사이 클릭 화합물, 융합 링
- 조사 기술
- 시편 처리
- 임상 실험실 기술
- 진단 기술 및 절차
- 진단
- 수술 절차, 수술
- 세포 학적 기술
- 세포 진단
- Camptothecin
- 알칼로이드
- 효소 및 코엔자임
- 항체
- 면역 글로불린
- 면역 단백질
- 혈액 단백질
- 혈청 글로불린
- 글로불린
- 무기 화학 물질
- 염소 화합물
- 질소 화합물
- 조정 복합체
- 데 옥시 시티 딘
- 시티 딘
- 피리 미딘 뉴 클레오 시드
- 피리 미딘
- 강요
- 궤조
- 진단 기술, 수술
- 화학 기술, 분석
- 스펙트럼 분석
- Formyltetrahydrofolates
- 테트라 하이드로 폴 레이트
- 엽산
- Pterins
- Teridines
- 우라실
- 피리 미디 논
- 금속, 무겁다
- 코엔자임
- 면역 글로불린 이소 타입
- 황화물
- 음이온
- 이온
- 전해질
- 황화수소
- 백금 화합물
- 전환 요소
- 옥살리플라틴
- 이리노테칸
- 젬시타빈
- 플루오로우라실
- 류코보린
- 면역글로불린 G
- 시스플라틴
- 1,2-디아미노사이클로헥산백금 II 구연산염
- 생검
- 자기 공명 분광법
- Durvalumab
- 이황화
- 백금
- 짐베 렐리 맙
- Dehydroftorafur
기타 연구 ID 번호
- 25-2512
- NCI-2026-03183 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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