- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07583914
Safety, Tolerability, and Preliminary Antitumor Activity of Non-Cationic Peptide-CD47 siRNA in Advanced Solid Tumors
2026년 5월 6일 업데이트: Xingchen Peng, West China Hospital
A Clinical Trial of Non-cationic Peptide-CD47 siRNA for Safety, Tolerability, and Preliminary Antitumor Activity in Patients With Advanced Malignant Solid Tumors
This study evaluates a non-cationic peptide-CD47 siRNA nanocomplex for refractory advanced solid tumors.
The candidate blocks the CD47-SIRPα "don't eat me" signal, repolarizes tumor-associated macrophages, and restores antitumor immunity.
Using a 3+3 dose-escalation design (25, 50, 100 μg), the investigators aim to define the MTD and RP2D, providing a novel therapeutic approach and clinical evidence for siRNA drug development.
연구 개요
상세 설명
This is a single-arm, open-label, non-randomized, single-center, prospective phase 1 clinical study conducted to evaluate the safety, tolerability, and preliminary antitumor activity of intratumorally injected NCP-CD47 siRNA in participants with advanced solid tumors.
The primary objective is to assess the safety and tolerability of the NCP-CD47 siRNA formulation, and the secondary objective is to evaluate its preliminary antitumor activity.
Safety refers to the frequency and severity of adverse events induced by NCP-CD47 siRNA, mainly assessed by the incidence of dose-limiting toxicities (DLTs), adverse events graded according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, and routine laboratory examinations including hematological and biochemical indicators.
Tolerability reflects participants' ability to tolerate adverse events related to the study drug, mainly assessed by the number of treatment discontinuations due to treatment-related adverse reactions, as well as changes in physiological and biochemical parameters, body weight, and adverse event reports (CTCAE 5.0).
The primary endpoint is the incidence of DLTs and the number of treatment discontinuations due to treatment-related adverse reactions during the first treatment cycle of NCP-CD47 siRNA administration.
The secondary endpoints include objective response rate (ORR), disease control rate (DCR), time to first complete response (CR) or partial response (PR), duration of response (DOR, defined as the interval from the first confirmed CR or PR to the first disease progression or death from any cause), duration of stable disease (SD, defined as the interval from the first confirmed SD to the first disease progression or death from any cause), progression-free survival (PFS, defined as the interval from the first administration of NCP-CD47 siRNA to the first disease progression or death from any cause), and overall survival (OS, defined as the interval from the first administration of NCP-CD47 siRNA to death from any cause).
The study plans to enroll 3 to 18 participants with advanced solid tumors who have failed second-line chemotherapy, adopts a standard "3+3" dose-escalation design with three siRNA dose levels (25 μg, 50 μg, and 100 μg) and 3 participants enrolled in each dose cohort, administers the NCP-CD47 siRNA formulation via intratumoral injection, and ensures that the formulation is manufactured under GMP-compliant conditions, then aliquoted and reserved for clinical use in accordance with the clinical administration protocol.
연구 유형
중재적
등록 (추정된)
9
단계
- 1단계
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:
- Male or female patients aged ≥18 years and ≤70 years.
- Histopathologically confirmed advanced recurrent/metastatic malignant solid tumors that are refractory to second-line treatment and have no available standard clinical therapeutic options (e.g., advanced soft tissue sarcoma, advanced head and neck squamous cell carcinoma, malignant melanoma, etc.).
- Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1.
- Expected overall survival ≥3 months.
- Interval from the last chemotherapy, radiotherapy, or surgery ≥28 days.
- Interval from the last use of nitrosourea or mitomycin C ≥6 weeks.
- Adequate organ function, defined by the following laboratory parameters within 14 days prior to enrollment:
- Hemoglobin ≥90 g/L (no blood transfusion within 14 days).
- Absolute neutrophil count >1.5 × 10⁹/L.
- Platelet count ≥80 × 10⁹/L.
- Total bilirubin ≤1.5 × upper limit of normal (ULN).
- Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤2.5 × ULN (≤5 × ULN in case of liver metastasis).
- Creatinine clearance ≥60 mL/min (calculated by Cockcroft-Gault formula).
- Left ventricular ejection fraction (LVEF) ≥50%.
- Signed written informed consent.
Exclusion Criteria:
- Participation in another investigational drug clinical trial within 4 weeks.
- Tumor located adjacent to major blood vessels or trachea.
- Uncontrolled cardiac clinical symptoms or diseases, including New York Heart -Association (NYHA) Class ≥2 heart failure, unstable angina, myocardial infarction within 1 year, or clinically significant supraventricular/ventricular arrhythmias requiring treatment or intervention.
- Female patients who are pregnant or lactating.
- Active pulmonary tuberculosis, bacterial or fungal infection (≥Grade 2 per NCI-CTCAE version 5.0), active human immunodeficiency virus (HIV) infection, active hepatitis B virus (HBV) infection, or hepatitis C virus (HCV) infection.
- History of uncontrollable psychoactive substance abuse or presence of mental disorders.
- Any active autoimmune disease or history of autoimmune disease, including but not limited to uveitis, enteritis, hypophysitis, nephritis, hyperthyroidism, and hypothyroidism. Subjects with vitiligo or childhood asthma in complete remission (no adult intervention required) are eligible; subjects with asthma requiring bronchodilator therapy are excluded.
- Receiving immunosuppressive therapy.
- History of drug abuse or known medical, psychological, or social conditions that interfere with study compliance (e.g., alcoholism or illicit drug addiction).
- Known hypersensitivity, allergy, or intolerance to the study drug NCP-CD47 siRNA (including any excipients), or history of severe allergic reactions to any drugs, foods, or vaccines (e.g., anaphylactic shock, allergic laryngeal edema, allergic dyspnea, allergic purpura, thrombocytopenic purpura, local Arthus reaction, etc.).
- Female subjects planning pregnancy, or male subjects whose partner plans pregnancy, from screening until 12 months after the last study drug injection.
- Any concomitant disease that, in the investigator's judgment, may seriously compromise patient safety or prevent the subject from completing the 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: 무작위화되지 않음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Intratumoral NCP-CD47 siRNA injection group
|
NCP-CD47 siRNA will be administered via intratumoral injection.
A total of 5 doses will be given, with subsequent doses administered once weekly after the first injection.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Number of Participants Experiencing Dose-Limiting Toxicities (DLTs)
기간: From the first dose to the end of treatment at 9 weeks
|
DLT is defined as any Treatment-Related Adverse Event (TRAE) or clinically significant laboratory abnormality occurring during the DLT observation period.
TRAEs include events judged by the investigator to be "definitely," "probably," or "possibly" related to the study treatment.
Severity will be graded according to NCI-CTCAE v5.0.
|
From the first dose to the end of treatment at 9 weeks
|
|
Number of participants with treatment discontinuation due to treatment-related adverse events during the first treatment cycle
기간: From the first dose to the end of treatment at 9 weeks
|
Treatment-related adverse events (TRAEs) will be assessed and graded according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
Treatment discontinuation is defined as permanent cessation of NCP-CD47 siRNA administration due to investigator-determined TRAEs occurring during the first treatment cycle.
|
From the first dose to the end of treatment at 9 weeks
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Progression-Free Survival
기간: Up to 6 months from the date of the first dose.
|
Progression-Free Survival (PFS) is defined as the time interval from the start of treatment until the first documented occurrence of disease progression (PD) according to RECIST v1.1, or death due to any cause, whichever occurs first.
|
Up to 6 months from the date of the first dose.
|
|
Overall Survival
기간: Up to 12 months from the date of the first dose.
|
OS is defined as the time interval from the start of treatment to death due to any cause.
For participants who are still alive at the end of the study, data will be censored at the last known date of follow-up.
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Up to 12 months from the date of the first dose.
|
|
Objective Response
기간: Time Frame: Up to 6 months from the date of the first dose.
|
Number of participants achieving a Best Overall Response (BOR) of either Complete Response (CR) or Partial Response (PR) according to RECIST v1.1.
Due to the small sample size, data will be reported as absolute counts.
|
Time Frame: Up to 6 months from the date of the first 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 (추정된)
2026년 5월 30일
기본 완료 (추정된)
2027년 6월 30일
연구 완료 (추정된)
2027년 12월 30일
연구 등록 날짜
최초 제출
2026년 4월 30일
QC 기준을 충족하는 최초 제출
2026년 5월 6일
처음 게시됨 (실제)
2026년 5월 13일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 5월 13일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 5월 6일
마지막으로 확인됨
2026년 5월 1일
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- 2026-892
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. .