- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07583914
Safety, Tolerability, and Preliminary Antitumor Activity of Non-Cationic Peptide-CD47 siRNA in Advanced Solid Tumors
6. Mai 2026 aktualisiert von: 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.
Studienübersicht
Status
Noch keine Rekrutierung
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Interventionell
Einschreibung (Geschätzt)
9
Phase
- Phase 1
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
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.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Number of Participants Experiencing Dose-Limiting Toxicities (DLTs)
Zeitfenster: 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
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Progression-Free Survival
Zeitfenster: 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
Zeitfenster: 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.
|
Up to 12 months from the date of the first dose.
|
|
Objective Response
Zeitfenster: 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.
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
30. Mai 2026
Primärer Abschluss (Geschätzt)
30. Juni 2027
Studienabschluss (Geschätzt)
30. Dezember 2027
Studienanmeldedaten
Zuerst eingereicht
30. April 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
6. Mai 2026
Zuerst gepostet (Tatsächlich)
13. Mai 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
13. Mai 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
6. Mai 2026
Zuletzt verifiziert
1. Mai 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 2026-892
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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