- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07649200
Study of SNH-118110 in Advanced Solid Tumors (SNH-118110)
A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of SNH-118110 in Patients With Advanced Solid Tumors
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Caicun Zhou, MD
- Numéro de téléphone: 86 021-58822171
- E-mail: CAICUNZHOUDR@TONGJI.EDU.CN
Lieux d'étude
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Chine, 200120
- The East Hospital Affiliated to Tongji University, Shanghai
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Safety evaluation
Délai: Up to approximately 2 years
|
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs).
|
Up to approximately 2 years
|
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Maximum tolerated dose (MTD) or maximum administered dose (MAD)
Délai: 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)
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
The maximum concentration (Cmax)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: Up to approximately 2 years
|
ORR of SNH-118110 evaluated by investigators per RECIST v1.1
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Up to approximately 2 years
|
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Disease control rate (DCR)
Délai: Up to approximately 2 years
|
DCR of SNH-118110 evaluated by investigators per RECIST v1.1
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Up to approximately 2 years
|
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Duration of response (DoR)
Délai: Up to approximately 2 years
|
DoR of SNH-118110 evaluated by investigators per RECIST v1.1
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Up to approximately 2 years
|
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Progression-free survival (PFS)
Délai: Up to approximately 2 years
|
PFS of SNH-118110 evaluated by investigators per RECIST v1.1
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Up to approximately 2 years
|
|
Overall survival (OS)
Délai: Up to approximately 2 years
|
Overall survival (OS)
|
Up to approximately 2 years
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Tumeurs par site
- Tumeurs
- Maladies des voies respiratoires
- Tumeurs par type histologique
- Maladies pulmonaires
- Tumeurs, glandulaires et épithéliales
- Adénocarcinome
- Tumeurs des voies respiratoires
- Tumeurs thoraciques
- Tumeurs pulmonaires
- Carcinome
- Tumeurs neuroectodermiques
- Tumeurs, cellules germinales et embryonnaires
- Tumeurs, tissu nerveux
- Carcinome bronchique
- Tumeurs bronchiques
- Tumeurs neuroendocrines
- Tumeurs canalaires, lobulaires et médullaires
- Carcinome neuroendocrinien
- Carcinome pulmonaire non à petites cellules
- Carcinome médullaire
Autres numéros d'identification d'étude
- SNH-118110-101
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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