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

국소 종양 내 N17350 투여를 통한 진행성 고형암 치료 (OP-NEU-101)

2026년 10월 16일 업데이트: Onchilles Pharma Inc

국소 진행성 고형 종양 환자에게 N17350을 종양 내 투여 시 안전성, 유효성 및 최적 용량 결정을 조사하기 위한 1/2상 개방형, 용량 탐색 및 확장 연구

The goal of this clinical trial is to learn if N17350 works to treat advanced solid tumors in adults. It will also learn about the safety of N17350 and help determine the best dose to use in future studies.

The main questions it aims to answer are:

  1. Does N17350 cause tumors to shrink or stop growing in some participants with advanced solid tumors?
  2. Are there any side effects for participants when taking N17350?
  3. What is the safest dose of N17350 and the dose that should be used for further study?
  4. Researchers will give N17350 directly into tumor lesions using a needle (intratumoral injection). This is an open-label study, meaning all participants will receive N17350 and there is no placebo.

Participants will:

  1. Receive injections of N17350 into tumor lesions every second week for 8 or 12 weeks
  2. Visit the clinic regularly for checkups, blood tests, and monitoring for side effects
  3. Have imaging scans (such as CT or MRI) to measure tumors and assess response
  4. Provide blood samples and, when required, tumor samples to help researchers understand how N17350 affects the tumor and the immune system

연구 개요

상태

모병

정황

개입 / 치료

상세 설명

This is a Phase 1/2 clinical study evaluating an investigational medicine called N17350 in adults with advanced solid tumors that have spread or cannot be removed by surgery and for which standard treatment options are no longer working, are not available, or are not appropriate.

N17350 will be administered by injection directly into tumor lesions (intratumoral injection). Giving N17350 into the tumor is intended to deliver treatment to the cancer site and may help stimulate an immune response against the tumor.

This is an open-label study, meaning all participants will receive N17350 and both participants and the study team will know the treatment being given. The study is designed to evaluate safety, identify an optimal dose, and look for early signs of anti-tumor activity.

Study Parts

The study includes two parts:

Part 1: Dose Finding (Phase 1) Small groups of participants will receive different dose levels of N17350. The main purpose is to understand how safe N17350 is and to determine a dose that can be given safely and is suitable for further study. Safety information from participants will be reviewed as dose levels are increased or adjusted.

Part 2: Dose Expansion (Phase 2) After a dose is selected from Part 1, additional participants will receive N17350 at that dose. This part is designed to better understand safety at the selected dose and to further evaluate how well N17350 may work in participants with advanced solid tumors. Depending on the study plan, expansion may include groups of participants with specific tumor types.

Treatment and Visits

Participants will receive N17350 injections into tumor lesions every second week for 8 or 12 weeks. Participants will attend clinic visits for treatment administration and ongoing monitoring.

Throughout the study, participants will undergo safety evaluations, which may include:

Review of side effects and other medical problems Physical examinations and vital signs Blood and urine tests Heart monitoring (such as ECG), if required Review of medications and overall health status

Participants will also undergo evaluations to measure how their cancer responds to treatment, which may include:

Imaging scans (such as CT or MRI) to measure tumors over time Clinical assessments of injected lesions and other tumor sites

Biomarker and Research Samples

The study may include collection of blood samples and, when required, tumor samples to help researchers understand how N17350 affects the tumor and the immune system. These samples may be used to study markers of immune activation and other biological changes that could be associated with response or side effects.

Outcomes and Goals

The main goals of the study are to:

Determine the type and frequency of side effects and evaluate overall safety

Identify a recommended dose and dosing approach for future studies

Evaluate early signs of treatment activity, such as tumor shrinkage, stable disease, or delayed tumor growth

Explore biological changes in blood and tumor tissue that may help explain how N17350 works

Study Hypothesis

The study hypothesis is that N17350 can be administered safely by intratumoral injection at doses that are tolerable, and that treatment may lead to anti-tumor effects in some participants with advanced solid tumors, potentially by helping the immune system recognize and attack cancer cells.

연구 유형

중재적

등록 (추정된)

275

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

  • 미국
    • California
      • Los Angeles, California, 미국, 90095
        • 모병
        • UCLA - Jonsson Comprehensive Cancer Center
        • 연락하다:
      • Los Angeles, California, 미국, 90025
        • 아직 모집하지 않음
        • The Angeles Clinic and Research Institute
        • 연락하다:
      • San Diego, California, 미국, 92037
      • San Francisco, California, 미국, 94143
        • 아직 모집하지 않음
        • University of California, San Francisco
        • 연락하다:
    • New York
      • Buffalo, New York, 미국, 14263
        • 모병
        • Roswell Park Comprehensive Cancer Center
        • 연락하다:
    • Texas
      • Houston, Texas, 미국, 77030
        • 모병
        • The University of Texas MD Anderson Cancer Center
        • 연락하다:
  • 호주
    • New South Wales
      • Newcastle, New South Wales, 호주, 2298
      • Westmead, New South Wales, 호주, 2145
    • Victoria
      • Melbourne, Victoria, 호주, 3550
        • 모병
        • Peter MacCallum Cancer Centre (PMCC)
        • 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

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Age ≥18 years (or legal age of consent in the study jurisdiction).

  2. Able to provide written informed consent and willing/able to comply with study procedures, visits, and follow-up.

  3. Advanced solid tumor malignancy (excluding lymphoma and other hematologic malignancies), with disease that has progressed on, is intolerant of, or is ineligible for standard therapies known to provide clinical benefit, or for whom no standard therapy is available.

  4. ECOG performance status 0-1.

  5. Measurable disease per IT-RECIST (Parts A1/A2) and RECIST v1.1 (Part A3), as applicable.

  6. At least one injectable tumor lesion, meeting superficial or visceral criteria and deemed safe/accessible for injection:

    1. Superficial lesions: ≥10 mm in longest diameter (or multiple lesions each ≥5 mm with aggregate longest diameter ≥10 mm), and ≤80 mm, accessible for direct injection (± ultrasound guidance).
    2. Visceral lesions: ≥10 mm and ≤50 mm in longest diameter, accessible for direct injection.
    3. Injected lesions must not involve/encase major blood vessels or otherwise pose an unacceptable bleeding/vascular risk, per investigator assessment and imaging review (as applicable).
    4. Expansion (Part A3): at least 1 measurable lesion and at least 1 additional injectable lesion suitable for injection.

  7. Adequate recovery from prior therapy: toxicities from prior anticancer treatment resolved to Grade ≤1 or baseline (except alopecia, controlled endocrine toxicities, or other stable toxicities as allowed per protocol/sponsor).

  8. Adequate organ function, including hepatic, renal, and coagulation parameters per protocol-defined thresholds.

  9. Adequate bone marrow function without transfusion support within 7 days prior to enrollment, per protocol-defined thresholds.

  10. Tumor tissue requirements: willingness to provide a pre-treatment tumor biopsy and on-study post-treatment biopsy, if an accessible lesion is available and safe for biopsy, and biopsy does not interfere with injection/response assessment; and/or availability of archival tumor tissue (obtained within 2 years prior to treatment), per protocol.

  11. Contraception requirements: participants of reproductive potential agree to use effective contraception and avoid pregnancy/fathering children from screening through 30 days after last dose; women of childbearing potential must have a negative pregnancy test within 14 days prior to first dose, per protocol.

Exclusion Criteria:

  1. Serious psychiatric, medical, or other condition that would interfere with study participation or protocol procedures, in the investigator's judgment.

  2. History of solid organ transplant.

  3. Alpha-1 antitrypsin deficiency.

  4. Hereditary or acquired bleeding disorder/coagulation factor deficiency.

  5. Active autoimmune disease requiring systemic treatment within the past 6 months, except clinically stable autoimmune conditions in remission not requiring systemic therapy (per protocol).

  6. Baseline QTcF >480 ms.

  7. Pregnant or breastfeeding.

  8. Prior severe immune-mediated adverse event (imAE) from immunotherapy: ≥Grade 3 imAE within the past 16 weeks, any Grade 4 life-threatening imAE, or any neurologic/ocular AE of any grade (except controlled endocrine AEs on stable replacement therapy per protocol).

  9. Another active malignancy (current or within the past 2 years) other than the disease under study, except specified low-risk cancers treated with curative intent or under active surveillance (per protocol).

  10. Recent anticancer therapy: receipt of systemic anticancer therapy (including investigational agents) within 2 weeks prior to first dose (or 4 weeks for monoclonal antibodies/ADCs/other long half-life biologics), or within 5 half-lives, whichever is shorter.

  11. Recent radiotherapy within 2 weeks prior to first dose.

  12. Unresolved toxicity from prior anticancer therapy to >Grade 1 or not at baseline (except Grade ≤2 neuropathy and other allowed exceptions per protocol).

  13. Uncontrolled or unstable brain metastases (eligible only if neurologically stable for ≥4 weeks, and off steroids or on stable/decreasing steroids ≤10 mg/day prednisone equivalent; carcinomatous meningitis excluded).

  14. Active infection requiring systemic antibacterial, antifungal, or antiviral therapy within 14 days prior to first dose.

  15. Chronic viral infections not meeting protocol criteria:

    1. HBV with detectable DNA unless on appropriate antiviral therapy
    2. Active HCV with detectable HCV RNA (treated HCV permitted if RNA undetectable)
    3. HIV infection with CD4+ count <300/μL, detectable viral load, or HIV-related illness within 6 months

  16. Use of systemic anticoagulants (e.g., warfarin, LMWH, DOACs) within 14 days prior to first dose.

  17. Chronic systemic corticosteroids >10 mg/day prednisone equivalent, or systemic immunosuppressive/anti-inflammatory medications within 4 weeks prior to first dose, except permitted topical/inhaled/local formulations or short courses for premedication per protocol.

  18. Known allergy/hypersensitivity to N17350 or any excipients.

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: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: N17350 Intratumoral Injection 1 mg/ml superficial lesions

Participants with superficial lesions will receive 1 mg/ml intratumoral N17350 injected into accessible tumor lesions every 2 weeks up to 12 weeks.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection 2 mg/ml superficial lesions

Participants with superficial lesions will receive 2 mg/ml intratumoral N17350 injected into accessible tumor lesions every 2 weeks up to 12 weeks.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection 4 mg/ml superficial lesions

Participants with superficial lesions will receive 4 mg/ml intratumoral N17350 injected into accessible tumor lesions every 2 weeks up to 12 weeks.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection 2 mg/ml visceral lesions

Participants with visceral lesions will receive 2 mg/ml intratumoral N17350 injected into accessible tumor lesions every 2 weeks up to 12 weeks.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection 4 mg/ml visceral lesions

Participants with visceral lesions will receive 4 mg/ml intratumoral N17350 injected into accessible tumor lesions every 2 weeks up to 12 weeks.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection for cuSCC

Participants with cuSCC superficial or visceral lesions will receive intratumoral N17350 injected into tumor lesions every 2 weeks up to 12 weeks at the recommended phase two dose.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection for Melanoma

Participants with Melanoma superficial or visceral lesions will receive intratumoral N17350 injected into tumor lesions every 2 weeks up to 12 weeks at the recommended phase two dose.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection for SCCHN

Participants with SCCHN superficial or visceral lesions will receive intratumoral N17350 injected into tumor lesions every 2 weeks up to 12 weeks at the recommended phase two dose.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection for NSCLC

Participants with NSCLC superficial or visceral lesions will receive intratumoral N17350 injected into tumor lesions every 2 weeks up to 12 weeks at the recommended phase two dose.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.
실험적: N17350 Intratumoral Injection for TNBC

Participants with TNBC superficial or visceral lesions will receive intratumoral N17350 injected into tumor lesions every 2 weeks up to 12 weeks at the recommended phase two dose.
생물학적: N17350

N17350 is a recombinant mutant porcine pancreatic elastase (PPE) developed to target the neutrophil elastase (ELANE) pathway.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Phase 1: Safety and tolerability of intratumoral N17350, including incidence of DLTs and adverse events
기간: DLTs: First 28 days; TEAEs/SAEs/laboratory abnormalities: From enrollment through 30 days after last dose assessed up to 4 months

Safety and tolerability will be assessed by the incidence and severity of dose-limiting toxicities (DLTs) and treatment-emergent adverse events (TEAEs), including serious adverse events (SAEs), and by laboratory abnormalities graded per CTCAE
DLTs: First 28 days; TEAEs/SAEs/laboratory abnormalities: From enrollment through 30 days after last dose assessed up to 4 months
Phase 2: Objective Response Rate (ORR) of lesions at RP2D/optimal dose(s)
기간: From baseline disease assessment until disease progression or initiation of a new anticancer therapy, assessed up to 15 months

ORR is defined as the proportion of participants with a best overall response of complete response (CR) or partial response (PR) in superficial and/or visceral lesions, assessed in separate tumor-specific expansion cohorts at the selected optimal dose(s)/RP2D(s), per protocol-defined response criteria
From baseline disease assessment until disease progression or initiation of a new anticancer therapy, assessed up to 15 months

2차 결과 측정

결과 측정
측정값 설명
기간
Objective Response Rate (ORR) in lesions (Phase 1)
기간: From first dose through end of treatment (up to 12 weeks) and follow-up tumor assessments, assessed up to 12 months

ORR is defined as the proportion of participants with a best overall response of CR or PR in superficial and visceral lesions, assessed during dose escalation and backfill cohorts per RECIST v1.1 and/or IT-RECIST, as applicable
From first dose through end of treatment (up to 12 weeks) and follow-up tumor assessments, assessed up to 12 months
Systemic exposure (PK) of N17350 following intratumoral administration
기간: From first dose through 30 days after last dose, assessed up to 4 months.

Systemic exposure to N17350 will be assessed by serum concentrations of active and inactive N17350
From first dose through 30 days after last dose, assessed up to 4 months.
Systemic exposure (PK) of N17350 following intratumoral administration
기간: From first dose through 30 days after last dose, assessed up to 4 months.

Systemic exposure to N17350 will be assessed by serum concentrations of N17350, and derived PK parameter of Cmax
From first dose through 30 days after last dose, assessed up to 4 months.
Systemic exposure (PK) of N17350 following intratumoral administration
기간: From first dose through 30 days after last dose, assessed up to 4 months.

Systemic exposure to N17350 will be assessed by serum concentrations of N17350, and derived PK parameter of Tmax
From first dose through 30 days after last dose, assessed up to 4 months.
Systemic exposure (PK) of N17350 following intratumoral administration
기간: From first dose through 30 days after last dose, assessed up to 4 months.

Systemic exposure to N17350 will be assessed by serum concentrations of N17350, and derived PK parameter of area under the curve (AUC)
From first dose through 30 days after last dose, assessed up to 4 months.
Systemic exposure (PK) of N17350 following intratumoral administration
기간: From first dose through 30 days after last dose, assessed up to 4 months.

Systemic exposure to N17350 will be assessed by serum concentrations of N17350, and derived PK parameter of N17350 half life
From first dose through 30 days after last dose, assessed up to 4 months.
Immunogenicity of N17350 (anti-drug antibodies [ADA])
기간: From first dose through 30 days after last dose, assessed up to 4 months

Immunogenicity will be assessed by the incidence and titers of anti-drug antibodies (ADA) to N17350
From first dose through 30 days after last dose, assessed up to 4 months
Preliminary antitumor activity in lesions (ORR, DOR, DCR, CBR)
기간: From first dose until disease progression or start of new anticancer therapy, assessed up to 15 months

Antitumor activity in superficial and visceral lesions will be assessed by:

Objective Response Rate (ORR): proportion of participants with best overall response of CR or PR

Duration of Response (DOR): time from first documented response (CR or PR) to disease progression or death

Disease Control Rate (DCR): proportion of participants with best overall response of CR, PR, or SD

Clinical Benefit Rate (CBR): proportion of participants with CR, PR, or durable SD (as defined in the protocol)

Responses will be assessed per RECIST v1.1 and/or IT-RECIST, as applicable.
From first dose until disease progression or start of new anticancer therapy, assessed up to 15 months
Pharmacodynamic (PD) biomarkers
기간: From first dose through 30 days after last dose, assessed up to 4 months

Changes from baseline in PD biomarkers measured in blood and/or tumor samples, as applicable, following intratumoral administration of N17350
From first dose through 30 days after last dose, assessed up to 4 months
Progression-Free Survival (PFS) (Phase 2)
기간: From first dose until disease progression or death, assessed up to 15 months

PFS is defined as the time from first dose to disease progression or death from any cause, assessed per RECIST v1.1 and/or IT-RECIST, as applicable
From first dose until disease progression or death, assessed up to 15 months
Overall Survival (OS) (Phase 2)
기간: From first dose until death, assessed up to 15 months

OS is defined as the time from first dose to death from any cause.
From first dose until death, assessed up to 15 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

Onchilles Pharma Inc

협력자

Onchilles Pharma Pty Ltd

수사관

  • 연구 책임자: Emily Roberts-Thomson, Onchilles Pharma

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 5월 25일

기본 완료 (추정된)

2028년 7월 1일

연구 완료 (추정된)

2029년 11월 1일

연구 등록 날짜

최초 제출

2026년 1월 12일

QC 기준을 충족하는 최초 제출

2026년 1월 12일

처음 게시됨 (실제)

2026년 1월 14일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 21일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 16일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

키워드

추가 관련 MeSH 약관

기타 연구 ID 번호

  • OP-NEU-101

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

IPD 계획 설명

An IPD sharing plan has not yet been finalized. Any decision to share individual participant data will be determined after study completion and will consider participant privacy, informed consent, and applicable regulations.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

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