Golidocitinib in Patients With Mycosis Fungoides/Sézary Syndrome and T-Cell Large Granular Lymphocytic Leukemia (GEMSTONE)
A Pilot Study of Golidocitinib, a JAK1 Inhibitor, in Patients With Mycosis Fungoides/Sézary Syndrome and T-Cell Large Granular Lymphocytic Leukemia (GEMSTONE)
This is an open-label, single-institution pilot study of single-agent golidocitinib enrolling up to 24 patients in two cohorts: a) advanced-stage mycosis fungoides/Sézary syndrome (MF/SS), n=12, or b) T-cell large granular lymphocytic leukemia (T-LGLL) requiring treatment, n=12. Patients will receive single agent golidocitinib at the previously established dose of 150 mg QD as determined in the phase I and II studies of golidocitinib.
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
등록 (추정된)
등록
단계
단계
- 2 단계
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Neha Mehta-Shah, MD
- 전화번호: 557-747-2108
- 이메일: mehta-n@wustl.edu
연구 장소
-
-
Missouri
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St Louis, Missouri, 미국, 63110
- Washington University School of Medicine
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수석 연구원:
- Neha Mehta-Shah, MD
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부수사관:
- Fei Wan, PhD
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연락하다:
- Neha Mehta-Shah, MD
- 전화번호: 557-747-2108
- 이메일: mehta-n@wustl.edu
-
부수사관:
- Hunter C Cochran, MD
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부수사관:
- Todd Fehniger, MD, PhD
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부수사관:
- Jacqueline Payton, MD, PhD
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria for MF/SS:
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Histologically or cytologically confirmed mycosis fungoides or Sézary syndrome, stages IB to IVB with measurable disease and/or detectable blood involvement based on the Global Response Criteria for CTCL (Olsen et al., 2022).
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Received at least one prior line of systemic therapy.
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Requires systemic therapy for their CTCL, in the opinion of the treating physician.
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At least 18 years of age.
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ECOG performance status ≤ 2
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Adequate counts and organ function as defined below:
- Platelet count > 75 K/cumm, unless related to lymphoma, in which case platelet count must be > 50 K/cumm. Platelet transfusion may be utilized to meet inclusion criteria, as long as the platelet count remains at the above threshold without transfusion for 5 days.
- Estimated (as calculated by the Cockcroft-Gault method) or measured creatinine clearance ≥ 30 mL/min.
- Serum total bilirubin ≤ 1.5 x IULN if no liver involvement, or ≤ 2 x IULN in the presence of Gilbert's syndrome (unconjugated hyperbilirubinemia) or liver involvement.
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x IULN, or ≤ 5 x IULN if documented hepatic involvement with lymphoma.
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Able to swallow pills.
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The effects of golidocitinib on the developing human fetus are unknown. For this reason, women of childbearing potential and men must agree to use highly effective methods of contraception for the duration of study participation and for 3 months after the last dose of golidocitinib for female patients and female partners of male patients, or for 6 months after the last dose of golidocitinib for male patients and male partners of female patients. Should a woman become pregnant or suspect she is pregnant or a male patient suspect he has impregnated another while participating in this study, s/he must inform the treating physician immediately.
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Ability to understand and willingness to sign an IRB approved written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of study participants.
Inclusion Criteria for LGLL
- Diagnosis of T-LGLL defined as: CD3+CD8+ cell population > 650/mm3 or CD3+CD8+CD57+ population > 500/mm3 and the presence of a clonal T-cell receptor (within 1 month of diagnosis).
Note: patients with MDS-like T-LGLL may be included with PI approval even if CD3+CD8+ cell population is < 650/mm3, though +TCR is required. Natural-Killer (NK) LGL is also permitted, provided there is a clonal NK-cell population noted with > 500 cells/mm3.
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Had at least one line of systemic therapy for T-LGLL.
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Require treatment for T-LGLL, as defined by meeting one or more of the below criteria:
- Symptomatic anemia with hemoglobin < 10 g/dL
- Transfusion-dependent anemia
- Neutropenia with absolute neutrophil count (ANC) < 0.5 K/cumm
- Neutropenia with ANC < 1.5 K/cumm with recurrent infections
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At least 18 years of age.
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ECOG performance status ≤ 2
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Adequate counts and organ function as defined below:
- Platelet count > 50 K/cumm. Platelet transfusion may be utilized to meet inclusion criteria, as long as the platelet count remains > 50 K/cumm within 5 days of last transfusion.
- Estimated (as calculated by the Cockcroft-Gault method) or measured creatinine clearance ≥ 30 mL/min.
- Serum total bilirubin ≤ 1.5 x IULN if no liver involvement, or ≤ 2 x IULN in the presence of Gilbert's syndrome (unconjugated hyperbilirubinemia) or liver involvement.
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x IULN, or ≤ 5 x IULN if documented hepatic involvement with T-LGLL.
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Patients with treated brain metastases are eligible if follow-up brain imaging after CNS-directed therapy shows no evidence of progression.
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Able to swallow pills.
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The effects of golidocitinib on the developing human fetus are unknown. For this reason, women of childbearing potential and men must agree to use highly effective methods of contraception for the duration of study participation and for 3 months after the last dose of golidocitinib for female patients and female partners of male patients, or for 6 months after the last dose of golidocitinib for male patients and male partners of female patients. Should a woman become pregnant or suspect she is pregnant or a male patient suspect he has impregnated another while participating in this study, s/he must inform the treating physician immediately.
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Ability to understand and willingness to sign an IRB approved written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of study participants.
Exclusion Criteria for MF/SS:
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Active CNS lymphoma.
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A history of other malignancy, with the exception of prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
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Currently receiving any other investigational agents.
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Concomitant use of another systemic therapy for MF/SS. Patients must have the following minimum washout from previous treatments:
- At least 8 weeks for low-dose (12 Gy or less) total skin electron beam therapy (TSEBT).
- At least 4 weeks for systemic cytotoxic anticancer agents or for tumor-targeting monoclonal antibodies (mAbs), with the exception of alemtuzumab, for which the washout is at least 16 weeks.
- At least 2 weeks or 5 half-lives (whichever is shorter) for systemic retinoids, interferons, vorinostat, romidepsin, and denileukin diftitox, or anticancer investigational agents that are not defined as immunotherapy.
- At least 1 week for topical retinoids, nitrogen mustard, or imiquimod.
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Receipt of medications or herbal supplements known to be strong inhibitors of CYP3A4 within the following time frames prior to the first dose of golidocitinib:
- 7 days for Ketoconazole, itraconazole, indinavir, saquinovir, nelfinavir, atazanavir, amprenavir, fosamprenavir, troleandomycin, telithromycin, fluconazole, nefazodone, cimetidine, aprepitant, miconazole, fluvoxamine
- 14 days for Erythromycin, clarithromycin, verapamil, ritonavir, diltiazem
- 6 weeks for amiodarone
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Receipt of medications known to prolong the QT interval within the following time frames:
- 2 days for clarithromycin, droperidol, erythromycin, procainamide
- 14 days for Cisapride, disopyramide, dofetilide, domperidone, ibutilide, quinidine, sotalol, sparfloxacin, thioridazine
- 4 weeks for levomethadyl, methadone, pimozide
- 6 weeks for arsenic trioxide
- 8 weeks for pentamidine
- 52 weeks for chloroquine
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Gastrointestinal disorders, or any other condition that may significantly interfere with absorption of the study medication by the investigator's assessment.
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Uncontrolled active infection requiring IV antibiotic, antiviral, or antifungal medications within 14 days before the first dose of study drug. Infections (e.g., urinary tract infection) controlled on concurrent antimicrobial agents and antimicrobial prophylaxis per institutional guidelines are acceptable.
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Current known active or chronic infection with HIV, hepatitis B, or hepatitis C. All patients will require serologic testing to be performed within 6 months prior to C1D1.
- Patients with chronic HBV are defined as patients with positive hepatitis B serology: Patients with a negative HBsAg and a positive HBcAb require an undetectable/negative hepatitis B DNA test (e.g. polymerase chain reaction [PCR] test) to be enrolled and will require prophylactic antiviral treatment initiated prior to the first dose of study drug, and continued until approximately 6 to 12 months after completion of study drug(s).
- Patients with chronic HCV infection are defined as patients with a positive hepatitis C antibody (anti-HCV) test:
- Patients with a positive anti-HCV antibody test require a quantitative HCV RNA viral load test (e.g., polymerase chain reaction [PCR] test) to determine eligibility. Patients with a positive anti-HCV antibody and a detectable/positive HCV RNA (i.e., active chronic HCV infection) are not eligible.
- Patients with a positive anti-HCV antibody and an undetectable/negative HCV RNA (i.e., prior resolved infection or previously treated and cured HCV) are eligible for enrollment without antiviral treatment.
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Unstable or severe uncontrolled medical condition or any important medical or psychiatric illness or abnormal laboratory finding that would, in the investigator's judgment, increase the risk to the patient associated with his/her participation in this study.
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QTcF ≥ 480 msec.
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Pregnant and/or breastfeeding.
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Concurrent immune-suppressive therapy exceeding prednisone 20 mg equivalent.
Exclusion Criteria for LGLL
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Active CNS involvement with T-LGLL.
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A history of other malignancy with the exception of prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
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Currently receiving any other investigational agents, or receipt of another systemic therapy for T-LGLL within 14 days or 5 half-lives of the first dose of golidocitinib, whichever is shorter.
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Receipt of medications or herbal supplements known to be strong inhibitors or inducers of CYP3A4 within the following time frames prior to the first dose of golidocitinib:
- 7 days for Ketoconazole, itraconazole, indinavir, saquinovir, nelfinavir, atazanavir, amprenavir, fosamprenavir, troleandomycin, telithromycin, fluconazole, nefazodone, cimetidine, aprepitant, miconazole, fluvoxamine
- 14 days for Erythromycin, clarithromycin, verapamil, ritonavir, diltiazem
- 6 weeks for amiodarone
-
Receipt of medications known to prolong the QT interval within the following time frames:
- 2 days for clarithromycin, droperidol, erythromycin, procainamide
- 14 days for Cisapride, disopyramide, dofetilide, domperidone, ibutilide, quinidine, sotalol, sparfloxacin, thioridazine
- 4 weeks for levomethadyl, methadone, pimozide
- 6 weeks for arsenic trioxide
- 8 weeks for pentamidine
- 52 weeks for chloroquine
-
Gastrointestinal disorders, or any other condition that may significantly interfere with absorption of the study medication by the investigator's assessment.
-
Uncontrolled active infection requiring IV antibiotic, antiviral, or antifungal medications within 14 days before the first dose of study drug. Infections (e.g., urinary tract infection) controlled on concurrent antimicrobial agents and antimicrobial prophylaxis per institutional guidelines are acceptable.
-
Current known active or chronic infection with HIV, hepatitis B, or hepatitis C. All patients will require serologic testing to be performed within 6 months prior to C1D1.
- Patients with chronic HBV are defined as patients with positive hepatitis B serology: Patients with a negative HBsAg and a positive HBcAb require an undetectable/negative hepatitis B DNA test (e.g. polymerase chain reaction [PCR] test) to be enrolled and will require prophylactic antiviral treatment initiated prior to the first dose of study drug, and continued until approximately 6 to 12 months after completion of study drug(s).
- Patients with chronic HCV infection are defined as patients with a positive hepatitis C antibody (anti-HCV) test: Patients with a positive anti-HCV antibody test require a quantitative HCV RNA viral load test (e.g., polymerase chain reaction [PCR] test) to determine eligibility. Patients with a positive anti-HCV antibody and a detectable/positive HCV RNA (i.e., active chronic HCV infection) are not eligible. AND Patients with a positive anti-HCV antibody and an undetectable/negative HCV RNA (i.e., prior resolved infection or previously treated and cured HCV) are eligible for enrollment without antiviral treatment.
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Unstable or severe uncontrolled medical condition or any important medical or psychiatric illness or abnormal laboratory finding that would, in the investigator's judgment, increase the risk to the patient associated with his/her participation in this study.
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QTcF ≥ 480 msec.
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Pregnant and/or breastfeeding.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
실험적: Cohort 1: Advanced-stage mycosis fungoides/Sézary syndrome (MF/SS) - Golidocitinib
Patients with advanced-stage MF/SS will take golidocitinib as a 150 mg pill orally each day of a 28-day cycle. |
Golidocitinib is a JAK1 kinase inhibitor taken orally at a dose of 150mg. |
|
실험적: Cohort 2: T-cell large granular lymphocytic leukemia (T-LGLL) - Golidocitinib
Patients with T-LGLL will take golidocitinib as a 150 mg pill orally each day of a 28-day cycle. |
Golidocitinib is a JAK1 kinase inhibitor taken orally at a dose of 150mg. |
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Overall Response Rate (ORR)
기간: At four months after start of treatment
|
ORR is defined as the proportion of evaluable patients achieving complete response (CR) or partial response (PR). As assessed according to the Global Response Criteria for CTCL and and International Consensus Criteria for T-LGLL. |
At four months after start of treatment
|
2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Best overall response rate
기간: Through completion of treatment (estimated to be 12 months)
|
Best overall response rate is defined by the best response of a given patient while being evaluated on study as assessed according to the Global Response Criteria for CTCL and and International Consensus Criteria for T-LGLL. |
Through completion of treatment (estimated to be 12 months)
|
|
Complete response rate
기간: Through completion of treatment (estimated to be 12 months)
|
Complete response rate is defined as the percentage of patients treated achieving a complete response (CR) as assessed according to the Global Response Criteria for CTCL and and International Consensus Criteria for T-LGLL. |
Through completion of treatment (estimated to be 12 months)
|
|
Duration of response
기간: From date of first response through disease progression (estimated to be 22 months)
|
Duration of response is defined as the time from first initial response to progression of disease as assessed according to the Global Response Criteria for CTCL and and International Consensus Criteria for T-LGLL. |
From date of first response through disease progression (estimated to be 22 months)
|
|
Time to maximum response
기간: Through completion of treatment (estimated to be 12 months)
|
Time to maximum response is defined by the time from initiation of study therapy to the time to achieve the best response as assessed according to the Global Response Criteria for CTCL and and International Consensus Criteria for T-LGLL. |
Through completion of treatment (estimated to be 12 months)
|
|
Clinical benefit rate
기간: Through completion of treatment (estimated to be 12 months)
|
Clinical benefit rate is defined by the percentage of patients treated who have achieved a complete response (CR), partial response (PR) or have stable disease (SD) for 6 months or greater as assessed according to the Global Response Criteria for CTCL and and International Consensus Criteria for T-LGLL. |
Through completion of treatment (estimated to be 12 months)
|
|
Frequency and grades of treatment-emergent adverse events (TEAE)
기간: From start of treatment through start of new treatment or 30 days after completion of treatment, whichever is earlier (estimated to be 13 months)
|
As assessed by CTCAE v6.0 |
From start of treatment through start of new treatment or 30 days after completion of treatment, whichever is earlier (estimated to be 13 months)
|
|
Rate of treatment discontinuation due to TEAE
기간: Through completion of treatment (estimated to be 12 months)
|
As assessed by CTCAE v6.0 |
Through completion of treatment (estimated to be 12 months)
|
공동 작업자 및 조사자
협력자
협력자
수사관
수사관
- 수석 연구원: Neha Mehta-Shah, MD, Washington University School of Medicine
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
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
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- 202609148
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
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