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A Clinical Study of MHB034C for Injection in Participants With Advanced Solid Tumors

2026년 11월 4일 업데이트: Minghui Pharmaceutical (Shanghai) LTD

A Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of MHB034C for Injection in Participants With Advanced Solid Tumors

This study is an open-label, multicenter, first-in-human (FIH) Phase I/II clinical study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, and preliminary efficacy of MHB034C in participants with advanced solid tumors.

연구 개요

상태

아직 모집하지 않음

상세 설명

The phaseI/II study consists of two stages: a dose escalation stage and a dose expansion stage. The primary objective of the Phase I dose escalation stage is to evaluate the safety and tolerability of MHB034C in participants with advanced solid tumors; the primary objective of the Phase II dose expansion stage is to evaluate the antitumor efficacy of MHB034C in selected participants with advanced solid tumors.

연구 유형

중재적

등록 (추정된)

400

단계

  • 2 단계
  • 1단계

연락처 및 위치

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

연구 연락처

연구 장소

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, 중국, 201419
        • Fudan University Shanghai Cancer Center
        • 연락하다:
          • Ethics Committee
          • 전화번호: 85033 +86 021-64175590
          • 이메일: JJYIN555@163.com

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

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Participants voluntarily agree to participate in this study and sign the informed consent form.
  2. Aged ≥ 18 years, regardless of sex.
  3. ECOG Performance Status (PS) score of 0-1.
  4. Life expectancy of more than 3 months.
  5. Female participants of childbearing potential, and male participants whose partners are women of childbearing potential, must agree to use highly effective contraception with their partners; must refrain from donating gametes, from initiating gamete cryopreservation, and from retrieving or using their own previously cryopreserved gametes for conception. Female participants of childbearing potential must have a negative serum β-HCG pregnancy test within 7 days prior to the first use of the investigational medicinal product (IMP), and must not be lactating.
  6. Ability to understand the study requirements and willingness and ability to comply with the study and follow-up procedures.
  7. Participants enrolled in the Phase I dose escalation stage must have advanced solid tumors confirmed by histopathological or cytological examination, and must have progressed on or been intolerant to standard therapy, or have no standard treatment available.
  8. Participants enrolled in the Phase II dose expansion stage must have advanced solid tumors confirmed by histopathological or cytological examination, and must have progressed on or been intolerant to standard therapy, or have no standard treatment available.
  9. During the dose escalation stage, the investigator should make best efforts to obtain consent from participants to provide pre-treatment tumor tissue samples; during the dose expansion stage, participants must agree to provide pre-treatment tumor tissue samples, and if such samples cannot be provided, enrolment is permitted only with the sponsor's approval.
  10. At least one measurable tumor lesion according to the RECIST v1.1 criteria.
  11. Adequate bone marrow function.
  12. Adequate hepatic function.
  13. Adequate renal function.
  14. Adequate coagulation function.
  15. Adequate cardiac function.

Exclusion Criteria:

  1. Has had another primary malignancy within 3 years prior to signing the informed consent form, excluding early-stage malignancies that have been curatively treated.
  2. Has previously used or is currently using an antibody-drug conjugate (ADC) with a topoisomerase I inhibitor as the payload, with certain exceptions.
  3. Has previously received doxorubicin at a cumulative dose of > 360 mg/m² or an equivalent dose of a similar agent.
  4. Has received chemotherapy or endocrine therapy within 3 weeks, or radiotherapy, biological therapy, immunotherapy, or other anti-tumor therapy within 4 weeks, prior to the first dose of the investigational medicinal product .
  5. Has spinal cord compression, leptomeningeal metastasis, brainstem metastasis, or unstable brain metastasis.
  6. Adverse events from prior anti-tumor therapy have not resolved to ≤ Grade 1 as assessed by NCI-CTCAE v6.0.
  7. Has undergone major surgery on a major organ (excluding biopsy) or experienced significant trauma within 4 weeks prior to the first use of the IMP, or requires elective surgery during the study period, or currently has severe unhealed or dehiscent wounds, active and clinically significant ulcers, untreated fractures, or active unhealed stomatitis.
  8. Has received a live vaccine or live attenuated vaccine within 4 weeks prior to the first use of the IMP.
  9. Has received or requires systemic corticosteroids or other immunosuppressive therapy within 14 days prior to the first use of the IMP, excluding topical, ophthalmic, intra-articular, intranasal, and inhaled corticosteroid therapy, and short-term corticosteroid use for prophylaxis.
  10. Has moderate or severe pulmonary disease that significantly impairs pulmonary function.
  11. Has a history of interstitial lung disease/pneumonitis (ILD), currently has ILD, or suspected ILD that cannot be ruled out by imaging during screening.
  12. Has severe cardiovascular disease or high-risk factors.
  13. Has experienced an arterial/venous thrombotic event within 6 months prior to the first dose.
  14. Has a clinically evident or uncontrolled third-space fluid collection requiring repeated drainage.
  15. Currently has an active autoimmune disease, or has a history of active autoimmune disease requiring systemic immunosuppressive therapy within 2 years prior to the first use of the IMP.
  16. Has clinically significant corneal disease, or is currently using other medications that may cause corneal damage.
  17. Has an active infection requiring systemic therapy within 7 days prior to the first dose.
  18. Has clinically uncontrolled diabetes mellitus.
  19. Has active tuberculosis, or a history of tuberculosis infection that was not controlled after treatment, or is still receiving anti-tuberculosis therapy; or has active syphilis.
  20. Positive serological virology results: positive for HIV antibody; or positive for HBsAg or HBcAb with HBV-DNA ≥ 500 IU/mL; or positive for HCV antibody with positive HCV-RNA.
  21. Has experienced clinically significant bleeding symptoms or an obvious bleeding tendency within 1 month prior to the first dose.
  22. Has known hypersensitivity or delayed hypersensitivity to certain components or analogues of the IMP in this study.
  23. Has a history of severe neurological or psychiatric disorders, or a history of psychotropic substance abuse or drug abuse, or any other medical condition.
  24. Has known alcohol or drug dependence.
  25. Has insufficient compliance to participate in this clinical study in the investigator's judgment, or the investigator considers that the participant has a history of other serious systemic diseases or other conditions unsuitable for participation in this study.

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: MHB034C for Injection

MHB034C for Injection

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Phase I Dose Escalation Stage: Incidence of DLT
기간: At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
Phase I Dose Escalation Stage: Incidence of Adverse events (AEs)
기간: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase I Dose Escalation Stage: Incidence of Serious adverse events (SAEs)
기간: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase I Dose Escalation Stage: MTD
기간: At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
Phase I Dose Escalation Stage: RP2D
기간: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: ORR as assessed by the investigator per RECIST v1.1.
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: DCR as assessed by the investigator per RECIST v1.1.
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: DoR as assessed by the investigator per RECIST v1.1.
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: PFS as assessed by the investigator per RECIST v1.1.
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: OS as assessed by the investigator per RECIST v1.1.
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: PFS rates at 6 and 12 months.
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: OS rates at 6 and 12 months.
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group

2차 결과 측정

결과 측정
기간
Phase I Dose Escalation Stage: AUC0-t、AUC0-∞ of MHB034C
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Cmax of MHB034C
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Tmax of MHB034C
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: CL of MHB034C
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: t1/2 of MHB034C
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Vss of MHB034C
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Ctrough of MHB034C
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage and Phase II Dose Expansion Stage: Positivity rate of anti-MHB034C antibodies (ADA) and their possible neutralizing antibodies (NAb)
기간: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: ORR as assessed by the investigator per RECIST v1.1
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: DCR as assessed by the investigator per RECIST v1.1
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: DoR as assessed by the investigator per RECIST v1.1
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: PFS as assessed by the investigator per RECIST v1.1
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: OS as assessed by the investigator per RECIST v1.1
기간: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: Incidence of AEs
기간: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: Incidence of SAEs
기간: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: Concentrations of total antibody, ADC, and free payload in participants after dosing
기간: through study completion, an average of 2 years
through study completion, an average of 2 years

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 (추정된)

2026년 12월 20일

기본 완료 (추정된)

2028년 6월 15일

연구 완료 (추정된)

2029년 5월 19일

연구 등록 날짜

최초 제출

2026년 10월 29일

QC 기준을 충족하는 최초 제출

2026년 11월 4일

처음 게시됨 (실제)

2026년 11월 10일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 10일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 4일

마지막으로 확인됨

2026년 11월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • MHB034C-A-101

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