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- Essai clinique NCT07811037
A Phase I/IIa Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, Immunogenicity, and Preliminary Efficacy of SGT003 in Patients With Advanced Solid Tumors
A Multicenter, Dose-Escalation and Expansion Phase I/IIa Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, Immunogenicity, and Preliminary Efficacy of SGT003 in Patients With Advanced Solid Tumors
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Shuchang Jiang
- Numéro de téléphone: +86 13552250017
- E-mail: shuchang.jiang@hotgen.com.cn
Lieux d'étude
-
-
Beijing Municipality
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Beijing, Beijing Municipality, Chine, 100142
- Recrutement
- Beijing Cancer Hospital
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Patient can fully understand the trial, participates voluntarily, and signs informed consent form (ICF) prior to any study procedures
- Patients aged 18 to 75 years at the time of ICF signature.
Study population:
- Phase I (dose-escalation study): Patients with advanced solid tumors confirmed histologically or cytologically, who have failed at least one standard therapy for advanced disease, are intolerant to standard therapy, or have no available standard treatment options.
- Phase IIa (dose-expansion study): Patients with advanced solid tumors who have received at least first-line but not up to third-line standard systemic therapy and experienced disease progression or intolerance to such therapy.
- ECOG 0 or 1.
- Radiographic evidence (CT/MRI, etc.) of disease progression documented during or after the most recent prior treatment.
- Patients must have adequate bone marrow reserve and organ function.
Exclusion Criteria:
- Subjects who have received chemotherapy, radiotherapy, biotherapy, endocrine therapy, immunosuppressive therapy or other anti-tumor therapy within 4 weeks prior to the first administration of the investigational product.
- Subjects who have received systemic immunosuppressant therapy within 14 days prior to the first administration of the investigational product.
- Subjects receiving anticoagulants such as therapeutic-dose heparin or vitamin K antagonists.
- Subjects who have received any live or attenuated live vaccine within 28 days prior to the first administration of the investigational product.
- Subjects who have undergone major surgery within 4 weeks prior to the first administration of the investigational product.
- Subjects with a history of Grade ≥3 immune-related adverse events (irAEs), hypersensitivity reactions, or Grade ≥2 immune-related myocarditis.
- Subjects with active autoimmune disease or prior autoimmune disease with a risk of recurrence. Exceptions: well-controlled type 1 diabetes, hypothyroidism controlled solely by hormone replacement therapy, and skin diseases that do not require systemic treatment.
- Subjects with current or prior active interstitial lung disease (ILD). Subjects with radiation-induced pulmonary fibrosis that does not require steroid therapy are eligible.
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: SGT003
Use SGT003 for Injection
|
Dosage Form: Injection Strength: 50 mg (5 mL) per vial Dosage and Administration: Subjects will receive SGT003 (investigational product) via intravenous (IV) infusion on Day 1 (D1) of each cycle. Dose: During the Phase I dose-escalation, subjects will be dosed according to the assigned dose cohort; during the Phase IIa dose-expansion stage, subjects will be dosed according to the selected expansion dose. Duration of Administration: For each subject, the first infusion will be completed within 90 minutes. If no infusion-related reaction (IRR) and/or hypersensitivity reaction occurs, the subsequent infusion duration may be shortened to no less than 60 minutes. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Adverse Events (AEs), immune-related Adverse Events (irAEs)
Délai: First dose up to 28 days (+3 days) after EOT, or prior to initiation of other anti-tumor therapy, whichever occurs first.
|
This includes clinically significant changes in vital signs, physical examination, electrocardiogram, echocardiogram and clinical laboratory tests, as graded by National Cancer Institute (NCI) Common Terminology for Adverse Events (CTCAE) version 6.0.
|
First dose up to 28 days (+3 days) after EOT, or prior to initiation of other anti-tumor therapy, whichever occurs first.
|
|
Phase I: Dose Limit Toxicity (DLTs)
Délai: Within the first dose cycle (Day1-Day21) of SGT003
|
Evaluated at each dose level of SGT003 graded by NCI CTCAE v6.0.
|
Within the first dose cycle (Day1-Day21) of SGT003
|
|
Phase I: Maximum Toxicity Dose(MTD)
Délai: Within the first dose cycle (Day1-Day21) of SGT003
|
The MTD is based on the incidence of DLTs
|
Within the first dose cycle (Day1-Day21) of SGT003
|
|
Phase I: Recommended Phase II dose (RP2D)
Délai: Within the first dose cycle (Day1-Day21) of SGT003
|
The RP2D is based on the results of safety、PK/PD and preliminary efficacy of SGT003 in the stage of dose escalation
|
Within the first dose cycle (Day1-Day21) of SGT003
|
|
Phase IIa: Objective Response Rate (ORR)
Délai: from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first. average Up to 24 months
|
The ratio of CR and PR Evaluated by RECIST1.1 and iRECIST,
|
from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first. average Up to 24 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Area under the plasma concentration-time curve (AUC)
Délai: From first study treatment to EOT, average of 24 months
|
area under the plasma concentration-time curve
|
From first study treatment to EOT, average of 24 months
|
|
Peak concentration (Cmax)
Délai: From first study treatment to EOT, average of 24 months
|
peak concentration
|
From first study treatment to EOT, average of 24 months
|
|
Time to peak concentration(Tmax)
Délai: From first study treatment to EOT, average of 24 months
|
time to peak concentration
|
From first study treatment to EOT, average of 24 months
|
|
Immunogenicity
Délai: Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
|
ADA detection rate, ADA incidence rate, Nab detection rate (if applicable), Nab incidence rate (if applicable)
|
Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Phase I. Objective Response Rate (ORR)
Délai: average Up to 24 months
|
Evaluated by RECIST1.1 and iRECIST, from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average Up to 24 months
|
|
Phase I and phase IIa. Duration of Response (DOR)
Délai: average Up to 24 months
|
Evaluated by RECIST1.1 and iRECIST, from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average Up to 24 months
|
|
Phase I and phase IIa. Disease Control Rate (DCR)
Délai: average Up to 24 months
|
The ratio of CR、PR and SD Evaluated by RECIST1.1 and iRECIST, whichever occurs first.
|
average Up to 24 months
|
|
Phase I and phase IIa. Time to Response (TTR)
Délai: average up to 24 months
|
The period from the date of randomization to the occurrence of CR/PR,evaluated by RECIST1.1 and iRECIST, , until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average up to 24 months
|
|
Phase I and phase IIa. Progression-Free Survival (PFS)
Délai: average Up to 24 months
|
from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
Evaluated by RECIST1.1 and iRECIST,
|
average Up to 24 months
|
|
Phase IIa. Overall Survival (OS)
Délai: average up to 24 months
|
the period from date of randomization to death
|
average up to 24 months
|
Collaborateurs et enquêteurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
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
Autres numéros d'identification d'étude
- SG-SGT003-101
- CTR20262751 (Identificateur de registre: China Center for Drug Evaluation (CDE), NMPA)
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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