To Evaluate the Safety and Tolerability of SYHX2001 in Patients With Advanced or Metastatic Solid Tumors
2022年8月8日 更新者:CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
This is a Phase 1, open-label, multicenter, dose escalation and expansion study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of the experimental drug(SYHX2001) in previously treated patients with advanced or metastatic cancer.
調査の概要
詳細な説明
This is a multicenter, open-label, dose-escalation, dose-expansion Phase 1 study of SYHX2001(name of the experimental drug) in patients with advanced or metastatic cancers who have exhausted standard treatment.
The study will consist of 2 parts, a dose escalation part and a cohort expansion part.
Once the recommended phase 2 dose (RP2D) has been determined in the dose escalation part, a cohort expansion part involving up to three separate cohorts will be conducted.
For patients, the study will include a screening phase, a treatment phase, and a post treatment follow-up phase.
An end-of-study visit will be conducted within 30 days after the last dose of SYHX2001.
研究の種類
介入
入学 (予想される)
176
段階
- フェーズ 1
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Xiaodong Wang
- 電話番号:+86 021-60673947
- メール:wang_xiaodong@mail.ecspc.com
研究場所
-
-
Heilongjiang
-
Harbin、Heilongjiang、中国
- 募集
- Harbin Medical University Cancer Hospital
-
コンタクト:
- Yanqiao Zhang, Professor
- 電話番号:13845120210
- メール:yanqiaozhang@126.com
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年~75年 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- Male or female patients with an age of 18~75years (inclusive).
- Confirmed histologic or cytologic diagnosis of an advanced and/or metastatic solid tumor.
- At least one measurable lesion as defined by RECIST version 1.1.
- Eastern Cooperative Oncology Group Performance Status 0 or 1.
- Life expectancy ≥3 months.
- Major organ function within 14 days prior to treatment meets the following criteria (no blood transfusion, Erythropoietin(EPO), Granulocyte Colony Stimulating Factor(G-CSF) or other medical support): Absolute Neutrophil Count(ANC)≥1.5×10^9/L,Platelet(PLT)≥90×10^9/L,Hemoglobin(Hb)≥100g/L or≥6.2 mmol/L;Creatinine(Cr)≤1.5×upper limit of normal(ULN) and creatinine clearance rate≥50mL/min;Total Bilirubin(TBIL)≤1.5×ULN; Prothrombin time(PT)≤1.5×ULN , Activated Partial Thromboplastin Time(APTT)≤1.5×ULN , Aspartate Aminotransferase(AST)/Alanine Aminotransferase(ALT)≤2.5 × ULN.
- Signed informed consent form.
Exclusion Criteria:
- Chemotherapy, radiotherapy, biotherapy, endocrine therapy, targeted therapy, immunotherapy and other anti-tumor treatment within 4 weeks prior to the first dose of the study drug, or administration of other investigational agents within 4 weeks or 5 half-lives prior to the first dose of the study drug, whichever is longer.
- Major surgery or significant trauma within 4 weeks prior to the first dose of the study drug.
- Adverse reactions from the previous anti-tumor treatment have not yet recovered to ≤ level 1 based on CTCAE 5.0。
- Have a history of severe cardiovascular and cerebrovascular disease.
- Central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence shows that the patient's central nervous system metastasis or meningeal metastasis has not been controlled and not suitable for the study according to the judgment of the investigator.
- Known history of hypersensitivity to test drug components.
- Patients with recent active bleeding or a history of bleeding.
- Those with coagulation disorders or taking thrombolytic, anticoagulant or antiplatelet agglutination drugs.
- Gastrointestinal perforation, abdominal fistula, or intra-abdominal abscess within 6 months prior to first dose; or currently under investigator's judgement there are high risk factors for hollow organ perforation/fistula formation).
- Inability to swallow the drug orally, or a condition that seriously affects gastrointestinal absorption in the judgment of the investigator.
- Irritable bowel syndrome with signs/symptoms requiring medication.
- Persistent active diarrhea requiring medical treatment.
- Concomitant use of strong CYP3A4 inhibitors or inducers, strong CYP2D6 inhibitors and strong P-gp inhibitors within 14 days prior to the first dose of the study drug.
- History of autoimmune diseases, immunodeficiency, including HIV positive, or other acquired, congenital immunodeficiency, or organ transplant history.
- Known Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), or other active viral infection.
- Male and female patients of childbearing potential do not agree to use suitable method of contraception during the treatment and 6 months after the last dose of study medication; female patients do not have negative results of serum/urine pregnancy test within 7 days prior to enrollment and would be breastfeeding.
- Not suitable for this study as determined by the investigator due to other reasons.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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 |
|---|---|
|
実験的:SYHX2001
SYHX2001 will be administered orally.
|
SYHX2001 tablets, oral
|
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 |
|---|---|
|
Dose limiting toxicities (DLT) in stage Ⅰ
時間枠:Baseline through Day 28
|
Baseline through Day 28
|
|
Maximum tolerated dose (MTD) in stage Ⅰ
時間枠:Baseline through Day 28
|
Baseline through Day 28
|
|
Recommended phase 2 dose (RP2D)
時間枠:Baseline through approximately 2 years
|
Baseline through approximately 2 years
|
|
Incidence and severity of adverse events in stage Ⅰ
時間枠:Baseline through approximately 2 years
|
Baseline through approximately 2 years
|
|
Overall response rate (ORR) in stage Ⅱ
時間枠:Up to approximately 2 years
|
Up to approximately 2 years
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Maximum observed plasma concentration (Cmax) of SYHX2001
時間枠:Baseline and up to approximately 2 years
|
Baseline and up to approximately 2 years
|
|
|
Area under the plasma concentration-time curve (AUC) extrapolated from time zero to infinity (AUC[0-inf]) of SYHX2001
時間枠:up to approximately 2 years
|
up to approximately 2 years
|
|
|
AUC from time zero to the last quantifiable concentration after dosing (AUC[0-t]) of SYHX2001
時間枠:up to approximately 2 years
|
up to approximately 2 years
|
|
|
Terminal phase half-life (t1/2) of SYHX2001
時間枠:up to approximately 2 years
|
up to approximately 2 years
|
|
|
Oral clearance (CL/F) of SYHX2001
時間枠:up to approximately 2 years
|
up to approximately 2 years
|
|
|
PFS Progression-free survival (PFS)
時間枠:up to approximately 2 years
|
PFS is defined as the time from first dose until radiographic progression per standard criteria or death due to any cause, whichever is earlier.
|
up to approximately 2 years
|
|
Duration of Response (DOR)
時間枠:up to approximately 2 years
|
DOR is defined as the time from first evidence of response (complete response or partial response per RECIST 1.1) to earlier date of disease progression or death due to any cause.
|
up to approximately 2 years
|
|
Number of patients with any adverse events(AEs) and serious adverse events(SAEs) in stage Ⅱ
時間枠:up to approximately 2 years
|
up to approximately 2 years
|
|
|
Change from Baseline in symmetrical arginine dimethylation (SDMA) as a pharmacodynamics(PD) measure
時間枠:Baseline and up to approximately 2 years
|
Baseline and up to approximately 2 years
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2022年7月27日
一次修了 (予想される)
2026年1月6日
研究の完了 (予想される)
2026年1月6日
試験登録日
最初に提出
2022年5月30日
QC基準を満たした最初の提出物
2022年6月3日
最初の投稿 (実際)
2022年6月7日
学習記録の更新
投稿された最後の更新 (実際)
2022年8月9日
QC基準を満たした最後の更新が送信されました
2022年8月8日
最終確認日
2022年8月1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
- SYHX2001C101
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?
未定
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
いいえ
米国FDA規制機器製品の研究
いいえ
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