- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07646106
THE-0504 in Patients With Solid Tumors
NANOFER-THE-0504: A Trial to Assess the Safety and Tolerability of an Investigational Drug THE-0504 for Patients With Solid Tumors
연구 개요
상세 설명
연구 유형
등록 (추정된)
단계
- 1단계
연락처 및 위치
연구 연락처
- 이름: Pierpaolo Ceci, PhD
- 전화번호: +39 0773822658
- 이메일: pierpaolo.ceci@thenabiotech.com
연구 연락처 백업
- 이름: Gennaro Daniele, PhD
- 전화번호: +39 0630157300
- 이메일: gennaro.daniele@policlinicogemelli.it
연구 장소
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Lazio
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Rome, Lazio, 이탈리아, 00168
- 모병
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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연락하다:
- Gennaro Daniele, PhD
- 전화번호: +39 0630157300
- 이메일: gennaro.daniele@policlinicogemelli.it
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
Patients will be enrolled in the study if they meet all the following criteria:
- written informed consent obtained;
- both gender adult (≥ 18 years) patients;
- diagnosis of solid tumor. Preferably, but non-limited, tumor types are the following: Small Cell Lung Cancer (SCLC), Colorectal Carcinoma (CRC), Pancreas Adenocarcinoma (PaAdCa), Gastric Cancer (GC) and Triple Negative Breast Cancer (TNBrCa);
- measurable metastatic disease or locally advanced unresectable tumors;
- have exhausted all EMA-approved treatment options;
- ECOG Performance Status graded as 0 or 1;
- patients able to understand the full nature and the purpose of the trial, including possible risks and side effects, able to cooperate with the Investigator and to comply with the requirements of the entire trial (ability to attend all the planned trial visits according to the time limits included) based on Investigator's judgement;
adequate liver function as assessed by following laboratory tests to be conducted within 28 days before the first dose of study treatment:
- Total bilirubin ≤ 1.5 × ULN (or ≤ 3 X ULN for patients with documented Gilbert-Meulengracht Syndrome, or for patients with hyperbilirubinemia considered due to liver metastasis).
- Aspartate transaminase and alanine transaminase ≤ 2.5 × ULN (or ≤ 5 × ULN if due to liver involvement by tumor);
adequate kidney function as assessed by following laboratory test to be conducted within 28 days before the first dose of study treatment:
• Estimated glomerular filtration rate (eGFR) ≥ 60 mL/min per 1.73 m2 according to the CKD-EPI formula.
adequate bone marrow function as defined as:
- Hgb ≥ 9 g/dL
- ANC ≥1.5x109/L
- PLT≥100.0 x109/L
- Female patients of childbearing potential and male patients who are sexually active with women of childbearing potential will have to mandatorily use an appropriate method of contraception, according to the definition of Note 3 of ICH M3 Guideline, for the entire duration of the trial and for a minimum of 12 months after last administration of the IMP.
Exclusion Criteria:
Patients will not be enrolled if they meet any of the following criteria:
- pregnant (as determined by a blood pregnancy test at the screening visit) or lactating women;
- male patients who are willing to father children during the trial or in the 12 months after the end of IMP administration;
- additional malignancy in the last 5 years. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or in situ cervical cancer that has undergone potentially curative therapy;
- have any unresolved toxicity of Grade ≥ 2 from previous anti-cancer treatment, except for alopecia and skin pigmentation. Patients with chronic, but stable Grade 2 toxicities may be allowed to enrol after agreement between the Investigator and Sponsor;
- ECOG Performance Status > 2;
- had not tolerated previously administered Top1 inhibitor treatments;
- known active CNS metastatic disease (patients with CNS metastases that are treated with radiotherapy and are stable for at least 28 days before study treatment start could be considered eligible);
- serious concurrent illness;
- Hgb < 9 g/dL;
- Transfusion dependent anemia with transfusion dependency of ≥3 months;
- Clinically significant iron metabolism disorders (e.g., sickle cell anemia) or use of iron chelators treatments;
- Iron overload, hereditary hemochromatosis and similar;
- Moderate (Child-Pugh B) or severe (Child-Pugh C) hepatic impairment;
- Prolonged QTc interval;
- Multiple Sclerosis (MS) or other demyelinating disease, Eaton-Lambert syndrome, history of haemorrhagic or ischemic stroke within the last 6 months, or alcoholic liver disease;
- Non-healing wound(s), except for ulcerative lesions caused by the underlying neoplasm;
- History of severe allergic or anaphylactic reactions to previous protein-based therapy;
- Currently receiving anticoagulation therapy with warfarin;
Known history of HIV infection, unless all the following are applicable:
- receiving an approved, stable, effective combination antiretroviral therapy regimen for ≥ 3 months prior to the planned first study intervention;
- CD4 T-cell count > 350 cells/μL
- CD4 T-cell nadir (lowest historical count) > 350 cells/μL, and • viral load confirmed as < 50 copies/mL.
- HBV infection, unless on stable anti-viral therapy for > 4 weeks prior to the planned first dose of study intervention and viral load confirmed as undetectable; and HCV infection, unless the participant has received curative treatment and viral load was confirmed as undetectable;
- Known autoimmune disease, uncontrolled diabetes, vitiligo, or stable thyroid disease;
- Patients on chronic (more than 10 days) administration of systemic, high-dose corticosteroids (≥4 mg Dexamethasone or equivalent), not amenable for reduction or suspension;
- Other concurrent medical or psychiatric conditions that, in the Investigator's opinion, may be likely to confound study interpretation or prevent completion of study procedures and follow-up examinations;
- History of drugs and/or alcohol abuse;
- Patients considered to be unsuitable to participate, in the Investigator's opinion, for any other reason (e.g. consequences of previous medical and/or surgical procedures or other medical or ethical reasons);
- Planned relocation during the study, which would make impossible to attend the scheduled visits and follow-ups;
- Concomitant participation in other clinical trials or participation in the evaluation of any investigational drugs/products up to 4 weeks before this trial (in any case, enrolment procedure should start only after the complete washout of the drugs/products under investigation**); or previous participation in the same trial or planned to receive other investigational products during the study.
공부 계획
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 |
|---|---|
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실험적: 치료 팔
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THE-0504 will be administered intravenously according to the treatment regimen specified in the protocol.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Assessment of Maximum Tolerated Dose (MTD)
기간: From enrollment to completion of Cycle 1 (each cycle is 21 days)
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From enrollment to completion of Cycle 1 (each cycle is 21 days)
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Assessment of Recommended Phase 2 Dose (RP2D)
기간: During dose escalation, at the end of cycle 1 (each cycle is 21 days)
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During dose escalation, at the end of cycle 1 (each cycle is 21 days)
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Pharmacokinetic assessments of the IMP
기간: Pre-dose and up to 96 hours (30 minutes, 3 hours, 24 hours, 48 hours and 96 hours) post-dose of the first 3 Cycles (63 days)
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Pre-dose and up to 96 hours (30 minutes, 3 hours, 24 hours, 48 hours and 96 hours) post-dose of the first 3 Cycles (63 days)
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Uprising / incidence of anti-THE-05 antibodies (ADA)
기간: From baseline through Cycle 4 (84 days)
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From baseline through Cycle 4 (84 days)
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Objective Response Rate (ORR) according to RECIST 1.1
기간: From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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Progression-Free Survival (PFS)
기간: From enrollment until disease progression or death from any cause (assessed up to 36 months)
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From enrollment until disease progression or death from any cause (assessed up to 36 months)
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Overall Survival (OS)
기간: From first IMP administration until death from any cause (assessed up to 36 months)
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From first IMP administration until death from any cause (assessed up to 36 months)
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Rate of patients with Complete Response (CR) or Partial Response (PR) according to RECIST 1.1
기간: From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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Assessment of safety profile of the product THE-0504
기간: From first IMP administration through 90 days after last IMP administration
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From first IMP administration through 90 days after last IMP administration
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ECOG Performance Status changes from baseline
기간: From baseline through 90 days after last IMP administration
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From baseline through 90 days after last IMP administration
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공동 작업자 및 조사자
수사관
- 수석 연구원: Gennaro Daniele, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- THE-0504-001
- 2023-503787-17-00 (씨티스)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
To the present date, only the sharing of the summary of the clinical results after 30 months from the study completion can be guaranteed.
Complete data from individual participants cannot be shared in scientific publications until intellectual property of the Investigational Medicinal Product is granted in all countries currently under evaluation.
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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