이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL

2026년 7월 29일 업데이트: Guangzhou Lupeng Pharmaceutical Company LTD.

A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Lacutoclax (LP-108) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

The goal of this clinical trial is to evaluate the efficacy and safety of Lacutoclax, an oral selective BCL-2 inhibitor, in patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). Lacutoclax is a potent and selective BCL-2 inhibitor with relatively weaker inhibitory activity against BCL-XL and BCL-W. Preliminary clinical data have demonstrated promising efficacy and an acceptable safety profile in patients with CLL/SLL and other B-cell non-Hodgkin lymphomas (B-NHLs). This is an open-label, single-arm, multicenter Phase II study evaluating the efficacy and safety of oral Lacutoclax tablets in patients with relapsed or refractory CLL/SLL.

연구 개요

연구 유형

중재적

등록 (추정된)

75

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Jiangsu
      • Nanjing, Jiangsu, 중국
        • 모병
        • The First Affiliated Hospital of Nanjing Medical University
        • 연락하다:

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:

  1. Patients with confirmed R/R CLL/SLL according to the 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria.
  2. Patients who had previously received standard therapy, experienced disease progression following the most recent line of treatment (excluding intolerance), and had at least one indication for treatment prior to enrollment.
  3. Have at least one measurable lesion.
  4. Age ≥18 years, regardless of sex.
  5. Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
  6. Life expectancy ≥ 12 weeks.
  7. Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
  8. Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
  9. Male patients and female patients of childbearing potential must agree to use effective contraception during the study and for 90 days after the last dose of Lacutoclax. Female patients of childbearing potential must have a negative pregnancy test before study treatment and must not be breastfeeding. Male patients must not donate sperm during the study and for 90 days after the last dose of Lacutoclax.
  10. Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.

Exclusion Criteria:

  1. Known hypersensitivity to Lacutoclax or any of its excipients.
  2. Prior treatment with a BCL-2 family inhibitor.
  3. History of or currently suspected Richter's syndrome.
  4. Known or suspected central nervous system (CNS) involvement.
  5. Prior allogeneic hematopoietic stem cell transplantation (allo-HSCT), or autologous hematopoietic stem cell transplantation (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days before the first dose of study treatment.
  6. Received antitumor therapy, investigational agents, major surgery, severe trauma, or live attenuated vaccines within 4 weeks or 5 half-lives prior to the first dose of study treatment.
  7. Received corticosteroids for antitumor purposes, herbal medicines for antitumor treatment, or localized radiotherapy within 14 days prior to the first dose of study treatment.
  8. Use of moderate or strong CYP3A inhibitors within 7 days prior to the first dose of study treatment, or consumption of grapefruit, grapefruit juice, starfruit, or Seville oranges within 3 days prior to dosing.
  9. Prior malignancy other than CLL/SLL within the past 2 years, except for curatively treated basal cell carcinoma, localized squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, or other malignancies considered cured.
  10. Major cardiovascular or cerebrovascular events within 6 months prior to the first dose of study treatment.
  11. Presence of any severe and/or uncontrolled systemic disease.
  12. Impaired cardiac function.
  13. Any uncontrolled systemic infection.
  14. Conditions that may impair oral drug administration or significantly affect absorption or pharmacokinetics of the study drug.
  15. Unable to discontinue moderate or strong CYP3A inhibitors or inducers, or sensitive CYP2C8 substrates during the study period.
  16. Primary autoimmune disease requiring immunosuppressive therapy.
  17. Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.

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: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Lacutoclax
All participants will receive oral Lacutoclax tablets once daily with dose escalation to a target dose of 400 mg.
Participants will first undergo a dose ramp-up period of at least 4 days (Cycle 0: C0D1-C0D4), followed by continuous administration at the target dose of 400 mg once daily starting from Cycle 1. Each treatment cycle will last 28 days. Treatment will continue until disease progression, unacceptable toxicity, or fulfillment of other criteria for treatment discontinuation.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Overall Response Rate (ORR) assessed by Independent Review Committee (IRC)
기간: Up to approximately 28 months
Up to approximately 28 months

2차 결과 측정

결과 측정
기간
ORR assessed by Investigator(INV)
기간: Up to approximately 28 months
Up to approximately 28 months
Complete response(CR) plus complete response with incomplete bone marrow recovery (CRi) rate (CRi applicable only to patients with CLL) assessed by IRC and INV, respectively
기간: Up to approximately 28 months
Up to approximately 28 months
Time to response (TTR) assessed by IRC and INV, respectively
기간: Up to approximately 30 months
Up to approximately 30 months
Duration of response (DOR) assessed by IRC and INV, respectively
기간: Up to approximately 30 months.
Up to approximately 30 months.
Time to first 50% reduction in absolute lymphocyte count (ALC) or normalization of ALC
기간: Up to approximately 28 months
Up to approximately 28 months
Progression-free survival (PFS) assessed by IRC and INV, respectively
기간: Up to approximately 30 months
Up to approximately 30 months
Overall Survival
기간: Up to approximately 30 months
Up to approximately 30 months
Adverse events(AEs) as assessed by CTCAE v5.0
기간: Up to approximately 30 months
Up to approximately 30 months
Adverse drug reactions (ADRs) related to Lacutoclax
기간: Up to approximately 30 months
Up to approximately 30 months
Serious adverse events (SAEs)
기간: Up to approximately 30 months
Up to approximately 30 months
Maximum Plasma Concentration(Cmax)
기간: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Time to Maximum Plasma Concentration (Tmax)
기간: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Half-life (T1/2)
기간: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Area Under the Plasma Concentration-Time Curve from Time Zero to Time t(AUC0-t)
기간: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

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)

2026년 7월 14일

기본 완료 (추정된)

2028년 3월 30일

연구 완료 (추정된)

2029년 9월 30일

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 7월 30일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 29일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

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. .

구독하다