A Study of HS-10587 in Patients With Advanced Solid Tumors
An Open-Label, Multi-Center Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic/Pharmacodynamic Characteristics, and Preliminary Efficacy of HS-10587 in Patients With Methylthioadenosine Phosphorylase (MTAP)-Deleted Advanced Solid Tumors
Přehled studie
Postavení
Postavení
Podmínky
Podmínky
Intervence / Léčba
Intervence / Léčba
Typ studie
Typ studie
Zápis (Odhadovaný)
Zápis
Fáze
Fáze
- Fáze 1
Kritéria účasti
Kritéria způsobilosti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
Inclusion Criteria:
- Participants who voluntarily participate in this clinical study, understand the study procedures, and are able to sign a written ICF.
- Participants with locally advanced or recurrent metastatic malignant solid tumors confirmed by histopathology or cytopathology who have failed or are intolerant to at least one line of prior standard treatment, or for whom no standard treatment exists.
- Evidence of MTAP deletion in the tumor tissue.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Life expectancy ≥12 weeks.
- At least one measurable lesion that would qualify as target lesion by Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1).
- Female participants of childbearing potential are willing to take appropriate contraceptive measures and should not breastfeed; male participants are willing to use barrier contraception.
Exclusion Criteria:
- History of other primary malignancies.
- Presence of pleural/abdominal effusion or pericardial effusion requiring clinical intervention.
- Presence of leptomeningeal metastasis, spinal cord compression, or brainstem metastasis; known untreated brain metastases, or symptomatic/unstable brain metastases.
- Participants who have any Grade ≥ 2 residual toxicity according to Common Terminology Criteria for Adverse Events (CTCAE, version 6.0) from prior anti-tumor therapies (except alopecia, pigmentation, and residual neurotoxicity).
- Inadequate bone marrow reserve or hepatic and renal functions.
- Severe, uncontrolled, or active cardiovascular diseases.
- Severe or poorly controlled diabetes.
- Severe or poorly controlled hypertension.
- Severe infection within 4 weeks prior to the first dose.
- Long-term corticosteroid therapy, history of other acquired/congenital immunodeficiency disorders, or organ transplantation.
- Known active infectious diseases.
- Clinically significant gastrointestinal dysfunction.
- Moderate to severe pulmonary diseases that seriously affect respiratory function.
- Prior history of severe neurological or mental disorders.
- Female participants who are pregnant or breastfeeding, or plan to become pregnant during the study.
- History of severe allergies, or history of hypersensitivity reactions to any active or inactive ingredients of HS-10587 or to drugs with similar chemical structures to HS-10587 or drugs of the same class as HS-10587.
- Participants with any conditions that may jeopardize participant safety or interfere with study assessments, as judged by the investigator.
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 |
|---|---|
|
Experimentální: HS-10587 Monotherapy
Dose escalation cohorts and dose expansion cohorts of varying doses of HS-10587
|
HS-10587 tablet
|
Co je měření studie?
Primární výstupní opatření
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Incidence of DLT
Časové okno: Up to 21 days after the first administration. (first cycle)
|
dose-limiting toxicities
|
Up to 21 days after the first administration. (first cycle)
|
|
MTD or MAD
Časové okno: Up to 21 days after the first administration. (first cycle)
|
maximum tolerated dose (MTD) or maximum applicable dose (MAD)
|
Up to 21 days after the first administration. (first cycle)
|
Sekundární výstupní opatření
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Incidence of adverse events (AEs) and serious adverse events (SAEs)
Časové okno: From time of informed consent to 28 days post last dose of HS-10587.
|
Number of participants with AEs and SAEs
|
From time of informed consent to 28 days post last dose of HS-10587.
|
|
Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors
Časové okno: Predose and postdose up to end of treatment, approximately 2 years
|
Maximum concentration (Cmax).
|
Predose and postdose up to end of treatment, approximately 2 years
|
|
Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors
Časové okno: Predose and postdose up to end of treatment, approximately 2 years.
|
Time of maximum concentration (Tmax).
|
Predose and postdose up to end of treatment, approximately 2 years.
|
|
Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors
Časové okno: Predose and postdose up to end of treatment, approximately 2 years.
|
area under the plasma concentration-time curve from time 0 to time t of the last measurable concentration (AUC0-t)
|
Predose and postdose up to end of treatment, approximately 2 years.
|
|
Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors
Časové okno: Predose and postdose up to end of treatment, approximately 2 years
|
Area under the plasma concentration-time curve from time 0 extrapolated to infinity (AUC0-∞)
|
Predose and postdose up to end of treatment, approximately 2 years
|
|
Efficacy of HS-10587 in patients with advanced solid tumors
Časové okno: Predose and post dose up to end of treatment, approximately 2 years
|
Objective response rate (ORR) evaluated as per RECIST v1.1
|
Predose and post dose up to end of treatment, approximately 2 years
|
|
Efficacy of HS-10587 in patients with advanced solid tumors.
Časové okno: Predose and post dose up to end of treatment, approximately 2 years.
|
Duration of response (DOR) evaluated as per RECIST v1.1
|
Predose and post dose up to end of treatment, approximately 2 years.
|
|
Efficacy of HS-10587 in patients with advanced solid tumors.
Časové okno: Predose and post dose up to end of treatment, approximately 2 years
|
Disease control rate (DCR) evaluated as per RECIST v1.1
|
Predose and post dose up to end of treatment, approximately 2 years
|
|
Efficacy of HS-10587 in patients with advanced solid tumors.
Časové okno: Predose and post dose up to end of treatment, approximately 2 years.
|
Time to response (TTR) evaluated as per RECIST v1.1
|
Predose and post dose up to end of treatment, approximately 2 years.
|
|
Efficacy of HS-10587 in patients with advanced solid tumors.
Časové okno: Predose and post dose up to end of treatment, approximately 2 years.
|
Progression-free survival (PFS) evaluated as per RECIST v1.1
|
Predose and post dose up to end of treatment, approximately 2 years.
|
|
Efficacy of HS-10587 in patients with advanced solid tumors.
Časové okno: Predose and post dose up to end of treatment, approximately 2 years
|
Overall survival (OS) evaluated as per RECIST v1.1
|
Predose and post dose up to end of treatment, approximately 2 years
|
Spolupracovníci a vyšetřovatelé
Sponzor
Sponzor
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
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
- HS-10587-101
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .