- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05407909
To Evaluate the Safety and Tolerability of SYHX2001 in Patients With Advanced or Metastatic Solid Tumors
8. august 2022 opdateret af: 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.
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
176
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Xiaodong Wang
- Telefonnummer: +86 021-60673947
- E-mail: wang_xiaodong@mail.ecspc.com
Studiesteder
-
-
Heilongjiang
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Harbin, Heilongjiang, Kina
- Rekruttering
- Harbin Medical University Cancer Hospital
-
Kontakt:
- Yanqiao Zhang, Professor
- Telefonnummer: 13845120210
- E-mail: yanqiaozhang@126.com
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 75 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: SYHX2001
SYHX2001 will be administered orally.
|
SYHX2001 tablets, oral
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Dose limiting toxicities (DLT) in stage Ⅰ
Tidsramme: Baseline through Day 28
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Baseline through Day 28
|
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Maximum tolerated dose (MTD) in stage Ⅰ
Tidsramme: Baseline through Day 28
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Baseline through Day 28
|
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Recommended phase 2 dose (RP2D)
Tidsramme: Baseline through approximately 2 years
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Baseline through approximately 2 years
|
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Incidence and severity of adverse events in stage Ⅰ
Tidsramme: Baseline through approximately 2 years
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Baseline through approximately 2 years
|
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Overall response rate (ORR) in stage Ⅱ
Tidsramme: Up to approximately 2 years
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Up to approximately 2 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Maximum observed plasma concentration (Cmax) of SYHX2001
Tidsramme: 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
Tidsramme: up to approximately 2 years
|
up to approximately 2 years
|
|
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AUC from time zero to the last quantifiable concentration after dosing (AUC[0-t]) of SYHX2001
Tidsramme: up to approximately 2 years
|
up to approximately 2 years
|
|
|
Terminal phase half-life (t1/2) of SYHX2001
Tidsramme: up to approximately 2 years
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up to approximately 2 years
|
|
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Oral clearance (CL/F) of SYHX2001
Tidsramme: up to approximately 2 years
|
up to approximately 2 years
|
|
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PFS Progression-free survival (PFS)
Tidsramme: 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.
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up to approximately 2 years
|
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Duration of Response (DOR)
Tidsramme: 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.
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up to approximately 2 years
|
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Number of patients with any adverse events(AEs) and serious adverse events(SAEs) in stage Ⅱ
Tidsramme: up to approximately 2 years
|
up to approximately 2 years
|
|
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Change from Baseline in symmetrical arginine dimethylation (SDMA) as a pharmacodynamics(PD) measure
Tidsramme: Baseline and up to approximately 2 years
|
Baseline and up to approximately 2 years
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
27. juli 2022
Primær færdiggørelse (Forventet)
6. januar 2026
Studieafslutning (Forventet)
6. januar 2026
Datoer for studieregistrering
Først indsendt
30. maj 2022
Først indsendt, der opfyldte QC-kriterier
3. juni 2022
Først opslået (Faktiske)
7. juni 2022
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
9. august 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
8. august 2022
Sidst verificeret
1. august 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- SYHX2001C101
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