A Phase 2 Study of Luvometinib Combined With Anlotinib in KRAS-mutated NSCLC
A Multicenter, Open-label, Single-arm Phase 2 Study to Evaluate the Efficacy and Safety of Luvometinib Combined With Anlotinib in Patients With KRAS-mutated Metastatic Non-small Cell Lung Cancer
調査の概要
状態
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:BAOHUI HAN
- 電話番号:+86 13817833343
- メール:18930858216@163.com
研究連絡先のバックアップ
- 名前:Wei Zhang
- 電話番号:+86 18017321318
- メール:zhwei2002@sjtu.edu.cn
研究場所
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200000
- 募集
- Shanghai Chest Hospital
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コンタクト:
- BAOHUI HAN
- 電話番号:+86 13817833343
- メール:18930858216@163.com
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コンタクト:
- Wei Zhang
- 電話番号:+86 18017321318
- メール:zhwei2002@sjtu.edu.cn
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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
- aged between ≥ 18 years and ≤75 years; regardless of male or female.
- Histologically and/or cytologically confirmed diagnosis of non-small cell lung caner,and the clinical stage is IV(AJCC 4th); Received at least one line of systemic treatment(including platinum-based chemotherapy ± PD-(L)1) during the stage IV, and disease progression occured during or after the treatment.
- KRAS mutation positive.
- ECOG score 0-1. 5. Expected survival time ≥ 3 months.
6.At least one intracranial measurable lesion according to RECIST v1.1 criteria.
7.Adequate organ function within 7 days before enrollment. 8. Recovery to ≤grade 1 or return to baseline from previous treatment-related adverse events (according to CTCAE 5.0), except for adverse events such as hair loss that are judged by the investigators to be safe and do not violate other inclusion criteria.
9. Avoid excessive exposure to sunlight, and be willing to use sufficient sunscreen when there is expected to be sunlight exposure.
10. Take contraceptive measures as required.
Exclusion Criteria
1.Patients who have previously received any of the following treatments:
- Prior treatment with MEK inhibitors、anlotinib or other VEGFR-TKI(such as cabozantinib, sorafenib, apatinib,etc);
- Major surgery within 28 days or minor surgery within 14 days prior to the first dose, or need to undergo major surgery during the study treatment;
- Systemic anti-cancer treatment (including chemotherapy, targeted therapy, immunotherapy, and other clinical trial drug treatments) within 28 days prior to the first dose or within 5 drug half-lives (whichever is shorter).
- Treatment with traditional Chinese medicine, Chinese patent medicine or modern Chinese medicine preparations with anti-tumor indications within 7 days prior to the first dose;
- Radical radiotherapy within 28 days prior to the first dose; palliative radiotherapy allowed if ≥14 days before first dose;
- Live or live-attenuated vaccine within 28 days prior to the first dose; other vaccines (e.g., inactivated COVID-19 vaccine) within 14 days prior to the first dose;
History of allogeneic organ transplantation or allogeneic stem cell transplantation, or autologous stem cell transplantation within 3 months prior to the first dose.
2.Active CNS metastases; brainstem, leptomeningeal, spinal cord metastases or spinal cord compression.
3.Small cell lung cancer (including mixed SCLC/NSCLC) or cavitary central squamous cell carcinoma.
4.Receipt of ≥4 prior lines of systemic anticancer therapy. 5.Active autoimmune disease requiring systemic therapy in the past 2 years,except: stable disease on replacement therapy without systemic treatment; non-systemic dermatologic conditions (vitiligo, psoriasis) or alopecia.
6.Active infection requiring systemic therapy within 2 weeks before first dose. 7.Uncontrolled hypertension. 8.Dysphagia, active gastrointestinal disease, malabsorption, or any condition impairing study drug absorption.
9.Retinal vein occlusion (RVO), retinal pigment epithelial detachment (RPED), uncontrolled glaucoma, or other ocular disease interfering with ocular toxicity assessment.
10.Current or previous idiopathic pulmonary fibrosis/pneumonitis; active ILD, pneumonitis (including clinically significant radiation pneumonitis), pulmonary fibrosis; history of tracheal fistula; continuous oxygen requirement due to severe dyspnea or respiratory insufficiency.
11.Active HBV or HCV; known AIDS or positive HIV; active tuberculosis or syphilis.
12.Tumor invasion into major vessels, heart, pericardium, trachea, esophagus, or high risk of esophagotracheal/esophagopleural fistula.
13.Significant hemoptysis within 1 month before first dose; clinically significant bleeding, bleeding tendency, coagulopathy, or history of ≥Grade 3 thrombosis.
14.Symptomatic or recurrent pleural effusion, ascites, or pericardial effusion requiring frequent drainage.
15.Other malignancy diagnosed within 5 years before first dose.
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:非ランダム化
- 介入モデル:順次割り当て
- 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:Arm1: safety run-in part
Oral treatment with luvometinib + anlotinib combination, including different doses.
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Dose A:luvometinib 8mg and anlotinib 8mg; Dose B1:luvometinib 12mg and anlotinib 8mg; Dose B2: luvometinib 8mg and anlotinib 10mg; Dose C: luvometinib 12mg and anlotinib 10mg.
他の名前:
in this part, patients will receive the combined treatment of luvometinib and anlotinib at the recommended doses.
他の名前:
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実験的:Arm2: expansion part
Select the optimal doses of luvometinib + anlotinib combination from the safety run-in period and continue enrolling about 30 patients to evaluate the efficacy and further safety.
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Dose A:luvometinib 8mg and anlotinib 8mg; Dose B1:luvometinib 12mg and anlotinib 8mg; Dose B2: luvometinib 8mg and anlotinib 10mg; Dose C: luvometinib 12mg and anlotinib 10mg.
他の名前:
in this part, patients will receive the combined treatment of luvometinib and anlotinib at the recommended doses.
他の名前:
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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 |
メジャーの説明 |
時間枠 |
|---|---|---|
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the objective response rate (ORR) per RECIST v1.1
時間枠:up to 24 months
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ORR assessed per RECIST v1.1 criteria,and defined as the proportion of patients with confirmed complete response (CR) and partial response (PR)
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up to 24 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Duration of overall response (DOR)
時間枠:up to 24 months
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DOR is defined as the time from the date of the first CR or PR to the first recorded tumor progression or death (death due to any cause), whichever occurs earlier
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up to 24 months
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Time to response (TTR)
時間枠:up to 24 months
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TTR is defined as the time from the first dose of the investigational drug to the first confirmed CR or PR
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up to 24 months
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Disease Control Rate (DCR)
時間枠:up to 24 months
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DCR is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease(SD)
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up to 24 months
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Progress Free Survival (PFS)
時間枠:up to 24 months
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PFS is defined as the time from the first dose to the first recorded progressive disease or death from any cause, whichever is first
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up to 24 months
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safety of the combination therapy of luvometinib and anlotinib
時間枠:up to 24 months
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including the types and frequencies of adverse event (AE) that occurred during the treatment period, Serious adverse events (SAE), adverse events that led to reduction of dose, and adverse events that resulted in discontinuation of dose.
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up to 24 months
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PK of the combination therapy of luvometinib and anlotinib
時間枠:up to 24 months
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including the types and frequencies of adverse event (AE) that occurred during the treatment period, Serious adverse events (SAE), adverse events that led to reduction of dose, and adverse events that resulted in discontinuation of dose.
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up to 24 months
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協力者と研究者
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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。