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
調査の概要
詳細な説明
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Pierpaolo Ceci, PhD
- 電話番号:+39 0773822658
- メール:pierpaolo.ceci@thenabiotech.com
研究連絡先のバックアップ
- 名前:Gennaro Daniele, PhD
- 電話番号:+39 0630157300
- メール:gennaro.daniele@policlinicogemelli.it
研究場所
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Lazio
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Rome、Lazio、イタリア、00168
- 募集
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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コンタクト:
- Gennaro Daniele, PhD
- 電話番号:+39 0630157300
- メール:gennaro.daniele@policlinicogemelli.it
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-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的:治療アーム
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THE-0504 will be administered intravenously according to the treatment regimen specified in the protocol.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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Assessment of Maximum Tolerated Dose (MTD)
時間枠: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)
時間枠: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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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Pharmacokinetic assessments of the IMP
時間枠: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)
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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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協力者と研究者
スポンサー
捜査官
- 主任研究者:Gennaro Daniele、Fondazione Policlinico Universitario Agostino Gemelli IRCCS
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- THE-0504-001
- 2023-503787-17-00 (Ctis)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
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.
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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