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
Přehled studie
Postavení
Postavení
Podmínky
Podmínky
Intervence / Léčba
Intervence / Léčba
Detailní popis
Typ studie
Typ studie
Zápis (Odhadovaný)
Zápis
Fáze
Fáze
- Fáze 2
- Fáze 1
Kontakty a umístění
Studijní kontakt
Studijní kontakt
- Jméno: Shuchang Jiang
- Telefonní číslo: +86 13552250017
- E-mail: shuchang.jiang@hotgen.com.cn
Studijní místa
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Beijing Municipality
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Beijing, Beijing Municipality, Čína, 100142
- Nábor
- Beijing Cancer Hospital
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Kritéria účasti
Kritéria způsobilosti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
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.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Počet zbraní
Zbraně a zásahy
Skupina účastníků / ArmSkupina účastníků / Arm |
Intervence / LéčbaIntervence / Léčba |
|---|---|
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Experimentální: 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. |
Co je měření studie?
Primární výstupní opatření
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Adverse Events (AEs), immune-related Adverse Events (irAEs)
Časové okno: 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.
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Phase I: Dose Limit Toxicity (DLTs)
Časové okno: Within the first dose cycle (Day1-Day21) of SGT003
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Evaluated at each dose level of SGT003 graded by NCI CTCAE v6.0.
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Within the first dose cycle (Day1-Day21) of SGT003
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Phase I: Maximum Toxicity Dose(MTD)
Časové okno: Within the first dose cycle (Day1-Day21) of SGT003
|
The MTD is based on the incidence of DLTs
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Within the first dose cycle (Day1-Day21) of SGT003
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Phase I: Recommended Phase II dose (RP2D)
Časové okno: Within the first dose cycle (Day1-Day21) of SGT003
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The RP2D is based on the results of safety、PK/PD and preliminary efficacy of SGT003 in the stage of dose escalation
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Within the first dose cycle (Day1-Day21) of SGT003
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Phase IIa: Objective Response Rate (ORR)
Časové okno: 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
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The ratio of CR and PR Evaluated by RECIST1.1 and iRECIST,
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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
|
Sekundární výstupní opatření
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Area under the plasma concentration-time curve (AUC)
Časové okno: From first study treatment to EOT, average of 24 months
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area under the plasma concentration-time curve
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From first study treatment to EOT, average of 24 months
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Peak concentration (Cmax)
Časové okno: From first study treatment to EOT, average of 24 months
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peak concentration
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From first study treatment to EOT, average of 24 months
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Time to peak concentration(Tmax)
Časové okno: From first study treatment to EOT, average of 24 months
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time to peak concentration
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From first study treatment to EOT, average of 24 months
|
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Immunogenicity
Časové okno: Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
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ADA detection rate, ADA incidence rate, Nab detection rate (if applicable), Nab incidence rate (if applicable)
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Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
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Další výstupní opatření
Další výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Phase I. Objective Response Rate (ORR)
Časové okno: average Up to 24 months
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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.
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average Up to 24 months
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Phase I and phase IIa. Duration of Response (DOR)
Časové okno: average Up to 24 months
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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.
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average Up to 24 months
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Phase I and phase IIa. Disease Control Rate (DCR)
Časové okno: average Up to 24 months
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The ratio of CR、PR and SD Evaluated by RECIST1.1 and iRECIST, whichever occurs first.
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average Up to 24 months
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Phase I and phase IIa. Time to Response (TTR)
Časové okno: average up to 24 months
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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.
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average up to 24 months
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Phase I and phase IIa. Progression-Free Survival (PFS)
Časové okno: average Up to 24 months
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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,
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average Up to 24 months
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Phase IIa. Overall Survival (OS)
Časové okno: average up to 24 months
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the period from date of randomization to death
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average up to 24 months
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Spolupracovníci a vyšetřovatelé
Sponzor
Sponzor
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Začátek studia
Primární dokončení (Odhadovaný)
Primární dokončení
Dokončení studie (Odhadovaný)
Dokončení studie
Termíny zápisu do studia
První předloženo
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
První zveřejněno
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Poslední zveřejněná aktualizace
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další identifikační čísla studie
Další identifikační čísla studie
- SG-SGT003-101
- CTR20262751 (Identifikátor registru: China Center for Drug Evaluation (CDE), NMPA)
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
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