Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

A Clinical Study of SHR-4685 on Safety, Tolerability and Pharmacokinetics in Participants With Solid Tumors

A Phase I Clinical Study of SHR-4685 on Safety, Tolerability and Pharmacokinetics in Participants With Solid Tumors

The study is being conducted to evaluate the safety, tolerability and pharmacokinetics of SHR-4685 in participants with advanced solid tumors.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

170

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

    • Beijing Municipality
      • Beijing, Beijing Municipality, Kina, 100142
        • Beijing Cancer Hospital
        • Ledende efterforsker:
          • Lin Shen
        • Kontakt:
        • Kontakt:
        • Ledende efterforsker:
          • Shaohua Ma

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

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  1. Have fully understood this study and voluntarily signed the informed consent form, with good compliance and cooperation with follow-up;
  2. Age 18-75 years, any gender;
  3. Performance status ECOG score 0 or 1;
  4. Expected survival time greater than 3 months;
  5. Presence of at least one measurable lesion according to RECIST 1.1 criteria;
  6. Have adequate organ function;
  7. Female participants of childbearing potential must have a negative serum pregnancy test within 7 days prior to the first dose; and must not be lactating.

Exclusion Criteria:

  1. Participants who have received any approved anti-tumor drugs (including investigational anti-tumor drugs) within 4 weeks prior to the first dose of the IP;
  2. Toxicities from prior anti-tumor therapy have not recovered to ≤ Grade 1 or to the level specified in the inclusion/exclusion criteria;
  3. Presence of central nervous system (CNS) metastases;
  4. Concurrent active malignancy other than the primary tumor;
  5. History of central nervous system diseases within 12 months prior to screening;
  6. Participants who have undergone major surgery other than diagnostic or biopsy procedures within 28 days prior to the first dose, or who are expected to undergo major surgery during the study;
  7. Participants with active tuberculosis or a history of active tuberculosis infection within ≤48 weeks prior to screening, regardless of treatment;
  8. Presence of any significant clinical or laboratory abnormality that, in the investigator's opinion, affects safety evaluation;
  9. History of deep vein thrombosis or pulmonary embolism within 6 months prior to screening;
  10. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring clinical intervention;
  11. Positive for human immunodeficiency virus (HIV) (HIV1/2 antibodies) with CD4+ T lymphocyte count <350 cells/uL; or history of other acquired/congenital immunodeficiency diseases; or history of allogeneic bone marrow or solid organ transplantation;
  12. Active chronic hepatitis B or active hepatitis C;
  13. Known history of hypersensitivity to any component of the formulations used in the study;
  14. Other factors, in the opinion of the investigator, that may affect the study results or result in forced halfway termination of this study, such as alcoholism, drug abuse, suffering from other serious diseases (including psychiatric disorders) requiring concomitant treatment, seriously abnormal laboratory test values, family or social factors and other conditions that may affect the safety of the patient or collection of study data.

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: SHR-4685 group
Participants will receive SHR-4685 in different doses.
SHR-4685, in different doses.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Dose-limiting toxicity (DLT) of SHR-4685.
Tidsramme: Up to 21 days.
Up to 21 days.
Maximum tolerated dose (MTD) of SHR-4685.
Tidsramme: Up to 24 months.
Up to 24 months.
Recommended Phase II Dose (RP2D) of SHR-4685.
Tidsramme: Up to 24 months.
Up to 24 months.
Adverse events (AEs).
Tidsramme: From the first drug administration to within 30 days for the last treatment dose, up to 24 months.
From the first drug administration to within 30 days for the last treatment dose, up to 24 months.
Serious adverse events (SAEs).
Tidsramme: From the first drug administration to within 30 days for the last treatment dose, up to 24 months.
From the first drug administration to within 30 days for the last treatment dose, up to 24 months.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
The concentration of SHR-4685 in plasma will be determined.
Tidsramme: At predefined intervals throughout the treatment period, up to 24 months.
Cmax will be derived.
At predefined intervals throughout the treatment period, up to 24 months.
Time to maximum concentration (Tmax).
Tidsramme: At predefined intervals throughout the treatment period, up to 24 months.
Evaluation of pharmacokinetic parameter of SHR-4685.
At predefined intervals throughout the treatment period, up to 24 months.
Area under the concentration-time curve from time 0 to time t (time of the last measurable concentration) (AUC0-t).
Tidsramme: At predefined intervals throughout the treatment period, up to 24 months.
Evaluation of pharmacokinetic parameter of SHR-4685. The concentration of SHR-4685 in plasma will be determined. Area under the curve is the integral of the concentration-time curve. The AUC reflects the actual body exposure to drug after administration. The AUC is dependent on the rate of elimination of the drug from the body and the dose administered.
At predefined intervals throughout the treatment period, up to 24 months.
The concentration of Anti-SHR-4685 antibodies (ADA) in plasma will be determined.
Tidsramme: At predefined intervals throughout the treatment period, up to 24 months.
At predefined intervals throughout the treatment period, up to 24 months.
Objective Response Rate (ORR).
Tidsramme: Up to 24 months.
Complete Response (CR) and Partial Response (PR) based on RECIST 1.1.
Up to 24 months.
Disease control rate (DCR).
Tidsramme: Up to 24 months.
Complete Response (CR), Partial Response (PR) and Stable Disease (SD) based on RECIST 1.1.
Up to 24 months.
Duration of response (DoR).
Tidsramme: Up to 24 months.
Time from documentation of tumor response to disease progression assessed among patients who had an objective response.
Up to 24 months.
Progression Free Survival (PFS).
Tidsramme: Up to 24 months.
Time from C1D1 to first assessment of disease progression or death, whichever is earlier.
Up to 24 months.

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 (Anslået)

1. juli 2026

Primær færdiggørelse (Anslået)

1. oktober 2028

Studieafslutning (Anslået)

1. oktober 2028

Datoer for studieregistrering

Først indsendt

24. juni 2026

Først indsendt, der opfyldte QC-kriterier

24. juni 2026

Først opslået (Faktiske)

30. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

30. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

24. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • SHR-4685-101

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

UBESLUTET

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

produkt fremstillet i og eksporteret fra U.S.A.

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Solid tumor

Kliniske forsøg med SHR-4685

Abonner