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A Multicenter, Randomized, Open-label, Parallel-group, Controlled, Superiority Phase III Clinical Study Comparing the Efficacy and Safety of F182112 Versus Standard of Care in Patients With Relapsed or Refractory Multiple Myeloma

2026년 5월 6일 업데이트: Shandong New Time Pharmaceutical Co., LTD

Phase III Clinical Study of F182112 in Patients With Relapsed or Refractory Multiple Myeloma

A Multicenter, Randomized, Open-label, Parallel-group, Controlled, Superiority Phase III Clinical Study Comparing F182112 with Standard of Care in Patients with Relapsed or Refractory Multiple Myeloma

연구 개요

상세 설명

This is a multicenter, randomized, open-label, parallel-group, controlled, superiority Phase III clinical study designed to compare the efficacy and safety of F182112 with standard of care in patients with relapsed or refractory multiple myeloma (RRMM). The study population consists of RRMM patients who have previously failed therapy with regimens containing at least one agent from each of the following three drug classes: proteasome inhibitors, immunomodulatory agents, and anti-CD38 monoclonal antibodies. The primary endpoint is PFS, with progression defined by IRC according to the 2016 IMWG criteria.

연구 유형

중재적

등록 (추정된)

261

단계

  • 3단계

연락처 및 위치

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

연구 연락처

연구 연락처 백업

연구 장소

      • Tianjing, 중국
        • 모병
        • Institute of Hematology & Blood Diseases Hospital
        • 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 must meet all of the following inclusion criteria to be eligible for enrollment in this study:
  2. Provide informed consent and voluntarily sign the informed consent form; Be male or female, aged ≥18 years;
  3. Have relapsed or refractory multiple myeloma (RRMM) who have previously failed therapy with regimens containing at least one agent from each of the following three drug classes: proteasome inhibitors, immunomodulatory agents, and anti-CD38 monoclonal antibodies; i. Relapsed: Disease progression requiring salvage therapy after achieving a minimal response (MR) or better following prior anti-myeloma therapy; ii. Refractory: Lack of response (failure to achieve MR or better) during the last anti-myeloma therapy, or disease progression within 60 days after the last anti-myeloma therapy;
  4. Before randomization, the investigator must pre-select a standard of care (SOC) treatment regimen based on the patient's disease status;
  5. Have an ECOG performance status of 0-2;
  6. Have at least one measurable disease parameter:

    • Serum M-protein ≥5 g/L;
    • Urine M-protein ≥200 mg/24 h;
    • Serum free light chain (FLC) assay: involved FLC level ≥100 mg/L with an abnormal serum FLC ratio (<0.26 or >1.65);
  7. Have organ function meeting the following requirements (no blood components or hematopoietic growth factors permitted within 7 days prior to first dose):

    • Hematology: Absolute neutrophil count (ANC) ≥1.0×10⁹/L, hemoglobin ≥70 g/L, platelets ≥50×10⁹/L;
    • Liver function: Total bilirubin ≤1.5×ULN, ALT ≤2.5×ULN, AST ≤2.5×ULN;
    • Renal function: Creatinine clearance ≥30 mL/min;
  8. All prior treatment-related toxicities (as defined by NCI CTCAE v6.0) must be ≤Grade 1 at screening, except for alopecia, non-clinically significant and asymptomatic Grade 2 laboratory abnormalities, and those parameters specifically permitted in the inclusion criteria;
  9. Have an expected survival of ≥3 months.

Exclusion Criteria:

  1. Central nervous system involvement or clinical symptoms of meningeal involvement by multiple myeloma;
  2. Concomitant light chain amyloidosis, plasma cell leukemia, Waldenström macroglobulinemia, or POEMS syndrome;
  3. History of any other malignancy within 3 years prior to first dose, except for malignancies with very low recurrence risk after curative treatment (e.g., squamous cell carcinoma or basal cell carcinoma of the skin, in situ cervical or breast cancer), or those who have undergone curative surgical resection (or other treatment) with no current evidence of disease and unlikely to impact survival during the study period;
  4. Dysphagia or active gastrointestinal dysfunction that may impair drug absorption;
  5. Evidence of cardiovascular risk, including any of the following:

    • QTc interval: ≥450 ms in males, ≥470 ms in females (QT interval must be corrected for heart rate using Friderici's formula);
    • Left ventricular ejection fraction (LVEF) <50%;
    • Electrocardiographic abnormalities deemed by the investigator to pose unacceptable risk, including clinically significant untreated or uncontrolled arrhythmias, second-degree (Mobitz II) or third-degree atrioventricular (AV) block;
    • History of myocardial infarction, acute coronary syndrome (including unstable angina), coronary angioplasty, stent placement, or bypass surgery within 6 months prior to screening;
    • Heart failure classified as NYHA Class III or IV;
    • Uncontrolled severe hypertension (systolic blood pressure ≥170 mmHg or diastolic blood pressure ≥110 mmHg);
  6. Active infection requiring antimicrobial, antiviral, or antifungal therapy (prophylactic therapy excluded):

    • Oral antimicrobial therapy within 2 weeks prior to first dose;
    • Intravenous antimicrobial therapy within 4 weeks prior to first dose;
    • History of viral respiratory infection (e.g., COVID-19, influenza A or B) within 2 weeks prior to first dose;
  7. Serological findings:

    • HBsAg positive and/or HbcAb positive with HBV-DNA positive or above upper limit of normal (ULN); HCV antibody positive with HCV-RNA positive or above ULN;
    • Active autoimmune disease, including HIV infection. Patients with well-controlled type 1 diabetes, euthyroid autoimmune thyroiditis, or skin diseases not requiring systemic therapy (e.g., vitiligo, psoriasis) are permitted;
    • Active syphilis infection;
    • Active tuberculosis (evidenced by chest imaging or other relevant testing within 3 months prior to screening or during screening; tuberculosis screening will be conducted per center protocol);
  8. Received live or attenuated vaccine within 4 weeks prior to first dose;
  9. Underwent major surgery within 4 weeks prior to first dose, or anticipated to undergo major surgery during the study period;
  10. Received the following anti-myeloma therapies prior to first dose:

    • Plasmapheresis within 28 days prior to first dose;
    • Monoclonal antibody therapy within 21 days prior to first dose;
    • Small molecule targeted therapy, cytotoxic chemotherapy, and/or proteasome inhibitor and/or other anti-tumor traditional Chinese medicine within 14 days or 5 half-lives (whichever is shorter) prior to first dose;
    • Systemic corticosteroids (prednisone >10 mg/day or equivalent dose) within 7 days prior to first dose;
    • Autologous stem cell transplantation within 3 months prior to first dose;
    • CAR-T or CAR-NK cell therapy within 3 months prior to first dose;
  11. Previously received allogeneic stem cell transplantation;
  12. Previously received BCMA-targeted therapy;
  13. Plan to receive other anticancer therapy or investigational drugs during the study period;
  14. Any severe and/or unstable pre-existing medical condition, psychiatric disorder, or other disease (including laboratory abnormalities) that may affect participant safety, informed consent acquisition, or adherence to study procedures;
  15. Pregnant or lactating women; male participants (or their partners) or female participants who plan to become pregnant during the study or within 6 months after the last dose, and who are unwilling to use a medically accepted effective contraceptive method (e.g., intrauterine device or condom) during the study period;
  16. Any patient deemed unsuitable for participation by the investigator..

    SAT-specific exclusion criteria:

  17. Inability to receive bortezomib as determined by the investigator;
  18. Contraindication to bortezomib or history of life-threatening allergic reaction or intolerance (defined as drug-related AE leading to discontinuation of treatment);
  19. Grade 1 peripheral neuropathy with pain or Grade ≥2 peripheral neuropathy;
  20. Received a strong CYP3A4 inducer within 5 half-lives prior to first dose;
  21. Previously received pomalidomide or have a contraindication to pomalidomide (e.g., history of arterial or deep vein thrombosis within the past 3 months [except intermuscular vein thrombosis], contraindication to or unwillingness to receive prophylactic antithrombotic therapy as required by protocol), or life-threatening allergic reaction or intolerance to pomalidomide;
  22. Previously received selinexor or have a contraindication to selinexor or life-threatening allergic reaction or intolerance to selinexor.

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: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: F182112 single-agent
F182112 single-agent
활성 비교기: PVd or SVd
Pomalidomide + Bortezomib + Dexamethasone (PVd) or Selinexor + Bortezomib + Dexamethasone (SVd)
Pomalidomide + Bortezomib + Dexamethasone (PVd) or Selinexor + Bortezomib + Dexamethasone (SVd)

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
the progression-free survival (PFS) evaluated by the Independent Review Committee (IRC) according to the 2016 IMWG criteria
기간: 2 year
2 year

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 1월 25일

기본 완료 (추정된)

2029년 1월 25일

연구 완료 (추정된)

2029년 1월 25일

연구 등록 날짜

최초 제출

2026년 5월 6일

QC 기준을 충족하는 최초 제출

2026년 5월 6일

처음 게시됨 (실제)

2026년 5월 12일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 12일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 6일

마지막으로 확인됨

2026년 1월 1일

추가 정보

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. .

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