- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07789327
Phase 1/2 Clinical Study of HY07121 for Injection (Subcutaneous) in Patients With Advanced Solid Tumors
An Open-label, Multiple-center, Phase 1/2 Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of HY07121 for Injection (Subcutaneous) in Patients With Advanced Solid Tumors
Studieoversikt
Status
Forhold
Detaljert beskrivelse
Studietype
Registrering (Antatt)
Fase
- Fase 2
- Fase 1
Kontakter og plasseringer
Studiekontakt
- Navn: Jinmin Yu, Doctor
- Telefonnummer: +86-521-67626971
- E-post: sdyujinming@126.com
Studer Kontakt Backup
- Navn: Hongxu Liu, Doctor
- Telefonnummer: +86-024-81916200
- E-post: liuhongxu3366@163.com
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Written informed consent;
- ≥18 years old and ≤80 years old, gender: male or female;
- Dose escalation part: cytologically or histopathologically confirmed locally advanced or advanced solid tumor that has failed standard therapy, or for which no standard therapy exists, or for which standard therapy is not tolerated or has been refused (for tumor types for which PD-1/PD-L1-related inhibitors are approved in China, failure of prior PD-1/PD-L1-related inhibitor therapy is required). Solid tumors in the dose expansion part include non-small cell lung cancer (driver gene-negative), gastric cancer, esophageal cancer, Microsatellite Instability-High / Mismatch Repair-Deficient Solid Tumors (MSI-H/dMMR) solid tumors, cervical cancer, non-muscle-invasive bladder cancer, head and neck squamous cell carcinoma (excluding nasopharyngeal carcinoma), renal cell carcinoma, and other tumor types;
- Dose escalation part: at least one evaluable tumor lesion is required. Dose expansion part: at least one measurable tumor lesion is required (per RECIST v1.1);
- Eastern Cooperative Oncology Group (ECOG) performance status score is 0 or 1;
- Life expectancy ≥3 months;
- Participant must have adequate main organ function;
- Fertile female patients must have a negative serological pregnancy test within 7 days before the first dosing and be willing to use effective birth control/contraception to prevent pregnancy during the study period up to 6 months after the last dosing of the study. Male patients must agree to have no sperm donation plans and to use effective contraceptive methods during the study period until 6 months after the last dose of the study.
- Postmenopausal women must have amenorrhea for at least 12 months before they are considered infertile.
Exclusion Criteria:
- Within the defined washout periods for prior anti-cancer treatments;
- Participant is currently participating or has participated in a study of an investigational agent or using an investigational device within 4 weeks of first dose of HY07121.
- Any other malignancy within 2 years prior to the first dose of the study treatment except for localized cancers that are considered to have been cured and in the opinion of the Investigator present a low risk for recurrence.
- Participant has not recovered (i.e., to Grade 1 or to baseline) from previous anticancer therapy-induced Adverse Events (AEs).
- Participants with a history of recently (within previous 2 years of the first dose of the study treatment) active diverticulitis or symptomatic peptic ulcer disease;
- Major surgery within 4 weeks of receiving the first dose of study treatment;
- Participant has Symptomatic Central Nervous System (CNS) metastases, or CNS metastases requiring CNS-directed local therapy (such as radiotherapy or surgery) or corticosteroids therapy within 4 weeks of first dose of study treatment;
- Participants with untreated or under treatment for tuberculosis, including but not limited to tuberculosis; Patients who have received standardized anti-tuberculosis treatment and have been confirmed cured by the researchers can be included;
- Participants with clinically significant cardiovascular diseases, in the past 6 months prior to the first dose of the study treatment; symptomatic coronary heart disease requiring drug treatment; arrhythmia requiring drug treatment; or uncontrolled hypertension;
- Known Human Immunodeficiency Virus (HIV) infection or known Acquired Immunodeficiency Syndrome (AIDS);
- Active or chronic hepatitis B or hepatitis C infection; treponema pallidum antibody positive, and confirmed positive test;
- Active known or suspected autoimmune disease.
- History of non-infectious pneumonitis that has required a course of oral or intravenous steroids to assist with recovery, or interstitial lung disease or severe obstructive pulmonary disease;
- History of severe allergy;
- History of allogeneic organ transplantation or graft-versus-host disease;
- Have received live/attenuated vaccines and messenger ribonucleic acid(mRNA) vaccines within 4 weeks prior to screening or plan to receive live/attenuated vaccines and mRNA vaccines during the study period;
- Any active infection requires systemic treatment via intravenous infusion within 4 weeks prior to the first dose of study treatment;
- Known psychiatric disorder or drug abuse that would interfere the trial requirements;
- Participant with uncontrolled pleural effusion, pericardial effusion or peritoneal effusion or need drainage;
- In addition to the tumors present at the time of entry into the study, other active malignancies were present within 3 years prior to the first dose (not excluding locally cured tumors, such as skin basal cell carcinoma, superficial bladder cancer or carcinoma in situ of the breast, etc.);
- Participants considered unsuitable for participation in this study by the investigators.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Sekvensiell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: : Test product HY07121 for Injection (Subcutaneous) for Dose Escalation
PART ONE- Dose escalation: HY07121 for Injection (Subcutaneous) should be administered Subcutaneously at recommended dose.
The purpose of the Dose Escalation Phase (Part one) is to characterize the safety and tolerability of the test product HY07121 for Injection (Subcutaneous) and determine the maximum tolerated dose (MTD) (if any) and/or the recommended dose(s) (RD) based on the frequency of the occurrence of Dose-Limiting Toxicity (DLT) in each cohort during the DLT evaluation period.
|
Dosage form: Powder for solution for infusion. Strength: 10 mg/vial. Method of administration: Subcutaneous administration. Dose escalation: "3+3" dose escalation rules are used to explore the safety and tolerability of the drug HY07121 for Injection (Subcutaneous).Based on emerging clinical data, dose escalation of an SUD-containing regimen may also follow a standard "3+3" design. Dose expansion: according to the preliminary safety and efficacy results of the dose escalation study, an appropriate dose and tumor species for the expansion study are conducted as discussed by the sponsor and investigators to further explore the safety and clinical effectiveness of the drug product HY07121 for Injection (Subcutaneous) and provide a basis for subsequent clinical studies.
Andre navn:
Dosage form: Powder for solution for infusion. Strength: 10 mg/vial. Method of administration: I Subcutaneous administration. Dose escalation: "3+3" dose escalation rules are used to explore the safety and tolerability of the drug HY07121 for Injection (Subcutaneous).Based on emerging clinical data, dose escalation of an SUD-containing regimen may also follow a standard "3+3" design. Dose expansion: according to the preliminary safety and efficacy results of the dose escalation study, an appropriate dose and tumor species for the expansion study are conducted as discussed by the sponsor and investigators to further explore the safety and clinical effectiveness of the drug product HY07121 for Injection (Subcutaneous) and provide a basis for subsequent clinical studies.
Andre navn:
|
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Eksperimentell: Test product HY07121 for Injection (Subcutaneous) for Dose Expansion
PART TWO- Dose expansion: HY07121 for Injection (Subcutaneous) should be administered Subcutaneously at recommended dose.
Patients will be administered a recommended dose of HY07121 for Injection (Subcutaneous) established from the Dose Escalation Phase of the study.
|
Dosage form: Powder for solution for infusion. Strength: 10 mg/vial. Method of administration: Subcutaneous administration. Dose escalation: "3+3" dose escalation rules are used to explore the safety and tolerability of the drug HY07121 for Injection (Subcutaneous).Based on emerging clinical data, dose escalation of an SUD-containing regimen may also follow a standard "3+3" design. Dose expansion: according to the preliminary safety and efficacy results of the dose escalation study, an appropriate dose and tumor species for the expansion study are conducted as discussed by the sponsor and investigators to further explore the safety and clinical effectiveness of the drug product HY07121 for Injection (Subcutaneous) and provide a basis for subsequent clinical studies.
Andre navn:
Dosage form: Powder for solution for infusion. Strength: 10 mg/vial. Method of administration: I Subcutaneous administration. Dose escalation: "3+3" dose escalation rules are used to explore the safety and tolerability of the drug HY07121 for Injection (Subcutaneous).Based on emerging clinical data, dose escalation of an SUD-containing regimen may also follow a standard "3+3" design. Dose expansion: according to the preliminary safety and efficacy results of the dose escalation study, an appropriate dose and tumor species for the expansion study are conducted as discussed by the sponsor and investigators to further explore the safety and clinical effectiveness of the drug product HY07121 for Injection (Subcutaneous) and provide a basis for subsequent clinical studies.
Andre navn:
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Doseeskalering (del 1): prosentandel av deltakerne som opplever behandlingsfremkommede bivirkninger (TEAE)
Tidsramme: Inntil 2 år
|
Forekomst og alvorlighetsgrad av uønskede hendelser (AE), alvorlige bivirkninger (SAE) og laboratorieavvik, i henhold til National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) versjon 5.0 og American Society for Transplantation and Cellular Therapy ( ASTCT) konsensusgradering
|
Inntil 2 år
|
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Doseeskalering (del 1): prosentandel av deltakerne som opplever bivirkningsrelaterte doseavbrudd, doseforsinkelser og doseintensitet
Tidsramme: Inntil 2 år
|
Forekomst av bivirkningsrelaterte doseavbrudd, doseforsinkelser og doseintensitet (varighet av eksponering for HY07121)
|
Inntil 2 år
|
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Doseutvidelse (del to): objektiv responsrate (ORR)
Tidsramme: Inntil 2 år
|
Andel deltakere som har bekreftet fullstendig respons (CR) eller delvis respons (PR)
|
Inntil 2 år
|
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Dose Escalation (Part One): Incidence and Nature of Dose-Limiting Toxicity (DLT)
Tidsramme: 28 days during the first 4-week cycle
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Dose-Limiting Toxicity (DLT) will be defined using National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
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28 days during the first 4-week cycle
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Doseutvidelse (del to): Prosentandel av deltakerne som opplever behandlingsfremkommede bivirkninger (TEAE)
Tidsramme: Inntil 2 år
|
Forekomst og alvorlighetsgrad av uønskede hendelser (AE), alvorlige bivirkninger (SAE) og laboratorieavvik, i henhold til National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) versjon 5.0 og American Society for Transplantation and Cellular Therapy ( ASTCT) konsensusgradering
|
Inntil 2 år
|
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Doseutvidelse (del to): prosentandelen av deltakerne som opplever uønskede hendelser (AE) relaterte doseavbrudd, doseforsinkelser og doseintensitet
Tidsramme: Inntil 2 år
|
Forekomst av uønskede hendelser (AE) relaterte doseavbrudd, doseforsinkelser og doseintensitet (varighet av HY07121 eksponering).
|
Inntil 2 år
|
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Doseeskalering og utvidelse: Vurdering av HY07121 Cmax
Tidsramme: Inntil 2 år
|
Maksimal konsentrasjon observert (Cmax) observert fra den farmakokinetiske profilen
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Inntil 2 år
|
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Doseeskalering og utvidelse: Vurdering av HY07121 AUC
Tidsramme: Inntil 2 år
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Areal under konsentrasjon kontra tid-kurven beregnet ved bruk av trapesmetoden
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Inntil 2 år
|
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Doseeskalering og utvidelse: Vurdering av HY07121 T1/2
Tidsramme: Inntil 2 år
|
Tiden det tar før halvparten av legemiddelkonsentrasjonen elimineres, beregnet ved å bruke helningen til terminallinjen
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Inntil 2 år
|
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Doseeskalering og utvidelse: Vurdering av HY07121 anti-medikament-antistoff (ADA)
Tidsramme: Inntil 2 år
|
Forekomst, varighet, titer av serum anti-HY07121 antistoff (ADA)
|
Inntil 2 år
|
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Doseeskalering (del 1): objektiv responsrate (ORR)
Tidsramme: Inntil 2 år
|
Andel deltakere som har en bekreftet fullstendig respons (CR) eller en delvis respons (PR) bestemt av etterforsker i henhold til responsevalueringskriteriene i solide svulster (RECIST) versjon 1.1
|
Inntil 2 år
|
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Doseeskalering og utvidelse: Varighet av respons (DOR) vurdert av etterforsker per responsevalueringskriterier i solide svulster (RECIST) versjon 1.1
Tidsramme: Inntil 2 år
|
Varighet av respons (DOR) er definert som tiden fra målekriteriene først er oppfylt for fullstendig respons (CR)/Delvis respons (PR) (avhengig av hva som først er registrert) til den første datoen for tilbakevendende eller progressiv sykdom.
|
Inntil 2 år
|
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Doseeskalering og utvidelse: Disease Control Rate (DCR) vurdert av etterforsker i henhold til RECIST versjon 1.1
Tidsramme: Inntil 2 år
|
Disease Control Rate er definert som prosentandelen av deltakerne som har oppnådd CR eller PR eller har vist stabil sykdom
|
Inntil 2 år
|
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Doseeskalering og utvidelse: Korrelasjonen mellom tumorbiomarkører og effekt
Tidsramme: Inntil 2 år
|
Objective Response Rate (ORR) er definert som andelen av deltakerne som har en bekreftet fullstendig respons (CR) eller en delvis respons (PR) bestemt av etterforsker per RECIST versjon 1.1.
Tumorbiomarkører vil bli testet ved hjelp av immunhistokjemi (IHC) og skåret ved bruk av Tumor Proportion Score (TPS) og/eller Combined Positive Score (CPS) algoritme.
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Inntil 2 år
|
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Dose Escalation and Expansion: Progression-Free Survival (PFS) assessed by investigator per RECIST Version 1.1
Tidsramme: Up to 2 years
|
Progression-Free Survival (PFS) is defined as the time from the date of first administration of HY07121 for Injection (Subcutaneous) to the date of the first documented disease progression determined by Investigator as per RECIST 1.1 or death from any cause, whichever occurs first
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Up to 2 years
|
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Dose Escalation and Expansion: Time-To-Progression (TTP) assessed by investigator per RECIST Version 1.1
Tidsramme: Up to 2 years
|
Time-To-Progression (TTP) is defined as the time from the date of first administration of HY07121 for Injection (Subcutaneous) to the date of the first documented disease progression
|
Up to 2 years
|
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Dose Escalation and Expansion: Overall Survival (OS)
Tidsramme: Up to 2 years
|
Overall Survival (OS) is defined as the time from the date of first administration of HY07121 for Injection (Subcutaneous) to death due to any cause
|
Up to 2 years
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Samarbeidspartnere og etterforskere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- HY0007-SC-101
Legemiddel- og utstyrsinformasjon, studiedokumenter
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Studerer et amerikansk FDA-regulert enhetsprodukt
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