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Study of SNH-118110 in Advanced Solid Tumors (SNH-118110)

11. juni 2026 opdateret af: ScinnoHub Pharmaceutical Co., Ltd.

A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of SNH-118110 in Patients With Advanced Solid Tumors

This is a multicenter, open-label, Phase I clinical study to evaluate the safety, tolerability, pharmacokinetics, and efficacy of SNH-118110 administered orally. The study consists of a dose-escalation phase and a dose-expansion phase.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

This first-in-human, open-label, multicenter Phase I study is designed to assess the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of SNH-118110 administered orally. The study comprises two sequential parts: a dose-escalation phase to identify the maximum tolerated dose (MTD) or maximum administered dose (MAD), followed by a dose-expansion phase to further evaluate safety and anti-tumor activity. The primary endpoints include safety, MTD, and/or MAD.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

240

Fase

  • Fase 1

Kontakter og lokationer

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

Studiekontakt

Studiesteder

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Kina, 200120
        • The East Hospital Affiliated to Tongji University, Shanghai

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:

  • Ability to understand and voluntarily sign an informed consent form (ICF) prior to any study related procedures.
  • Age ≥ 18 years at the time of signing the ICF.
  • Histologically or cytologically confirmed diagnosis of advanced solid tumors, with the following additional requirements:

Dose-escalation phase: Patients with advanced solid tumors harboring a RET gene alteration who have failed standard therapy or are intolerant to standard therapy.

Dose-expansion phase:

Cohort 1: Locally advanced or metastatic NSCLC with RET gene fusion who have progressed after at least one prior line of therapy, which must include a RET inhibitor.

Cohort 2: Treatment-naïve patients with locally advanced or metastatic NSCLC harboring a RET gene fusion.

Cohort 3: Other advanced solid tumors harboring RET gene alterations.

  • At least one measurable target lesion according to RECIST version 1.1.
  • Documentation of a RET fusion or other activating RET gene alteration (based on a local or central laboratory report).
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, with no deterioration within the 2 weeks prior to the first dose of study drug.
  • Life expectancy of at least 3 months.

Exclusion Criteria:

  • Presence of other known oncogenic driver mutations.
  • Prior anti-tumor therapy within specified washout periods prior to first dose (e.g., small molecules, biologics, radiotherapy, major surgery), or failure to recover from clinically significant toxicities.
  • Clinically significant uncontrolled or active conditions, including but not limited to:

Inadequate bone marrow, hepatic, or renal function. Significant cardiovascular disease (e.g., uncontrolled hypertension, prolonged QTc, poor ejection fraction, recent thromboembolic events).

Active or uncontrolled infections, bleeding diathesis, or significant pleural/abdominal/pericardial effusion requiring intervention.

Central nervous system metastases unless stable and asymptomatic off steroids.

  • Conditions affecting oral drug absorption or gastrointestinal function.
  • History of severe allergic reactions to similar agents.
  • Pregnant or lactating women, or patients with serious concurrent medical or psychiatric conditions that would compromise safety or study compliance.

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: SNH-118110
Dose escalation: Multiple doses of SNH-118110 Dose expansion: MTD/MAD/recommended expansion dose
Participants will continue treatment until progression of disease or the end of the study.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Safety evaluation
Tidsramme: Up to approximately 2 years
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs).
Up to approximately 2 years
Maximum tolerated dose (MTD) or maximum administered dose (MAD)
Tidsramme: Cycle 1 (up to 21 days)
Determination of the MTD or MAD of oral SNH-118110 by the number of participants who experience a dose limiting toxicity (DLT)
Cycle 1 (up to 21 days)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
The maximum concentration (Cmax)
Tidsramme: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
Cmax of SNH-118110
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
Time of the maximum concentration (Tmax)
Tidsramme: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
Tmax of SNH-118110
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
Area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC0-t)
Tidsramme: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
AUC0-t of SNH-118110
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
Elimination half-life (t1/2)
Tidsramme: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
T1/2 of SNH-118110
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
Objective response rate (ORR)
Tidsramme: Up to approximately 2 years
ORR of SNH-118110 evaluated by investigators per RECIST v1.1
Up to approximately 2 years
Disease control rate (DCR)
Tidsramme: Up to approximately 2 years
DCR of SNH-118110 evaluated by investigators per RECIST v1.1
Up to approximately 2 years
Duration of response (DoR)
Tidsramme: Up to approximately 2 years
DoR of SNH-118110 evaluated by investigators per RECIST v1.1
Up to approximately 2 years
Progression-free survival (PFS)
Tidsramme: Up to approximately 2 years
PFS of SNH-118110 evaluated by investigators per RECIST v1.1
Up to approximately 2 years
Overall survival (OS)
Tidsramme: Up to approximately 2 years
Overall survival (OS)
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 (Anslået)

26. juni 2026

Primær færdiggørelse (Anslået)

26. juni 2027

Studieafslutning (Anslået)

26. juni 2029

Datoer for studieregistrering

Først indsendt

11. juni 2026

Først indsendt, der opfyldte QC-kriterier

11. juni 2026

Først opslået (Faktiske)

16. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

16. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

11. juni 2026

Sidst verificeret

1. juni 2026

Mere information

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 .

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