- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07932873
Sonrotoclax in Combination With Azacitidine for Previously Untreated Higher-risk Myelodysplastic Syndromes
A Prospective, Single-Center, Phase Ⅱ Clinical Study on the Efficacy and Safety of Sonrotoclax Combined With Azacitidine in Previously Untreated Patients With Higher-risk Myelodysplastic Neoplasms
To evaluate the efficacy and safety profile of sotoclax combined with azacitidine in newly diagnosed higher-risk MDS patients, including ORR, CR rate, PFS, OS and treatment-related adverse events
Studieoversigt
Status
Betingelser
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 2
- Fase 3
Kontakter og lokationer
Studiekontakt
- Navn: Zhurhohan Yu
- Telefonnummer: +8617280290731
- E-mail: 1148629702@qq.com
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
-
Aged ≥ 18 years.
-
Diagnosed with myelodysplastic syndromes (MDS) based on bone marrow morphology, immunophenotyping, cytogenetics, and molecular testing, consistent with the WHO 2016 or 2022 classification criteria.
-
High-risk MDS defined by any of the following risk stratification systems:
- nbsp; a) IPSS-R score > 3.5; or
- nbsp; b) IPSS score > 1; or
- nbsp; c) IPSS-M score > 0.
-
No prior anti-tumor treatment for MDS, including hypomethylating agents or chemotherapy.
-
Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
-
Expected survival time ≥ 12 weeks.
-
Adequate major organ function as defined below:
- nbsp; a) Creatinine clearance ≥ 50 mL/min;
- nbsp; b) Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × upper limit of normal (ULN); Total bilirubin ≤ 1.5 × ULN;Left ventricular ejection fraction (LVEF) ≥ 45%.
-
Written informed consent must be obtained from the patient, legal representative, or guardian prior to any study-related procedures. The study protocol has been approved by the institutional ethics committee.
Exclusion Criteria:
- Diagnosis of acute promyelocytic leukemia (APL).
- Prior treatment with any BCL-2 inhibitor.
- History of other malignant tumors within the past 3 years (excluding cured malignancies).
- Presence of active and uncontrolled infectious diseases.
- Central nervous system (CNS) involvement.
- Severe and uncontrolled cardiac disease.
- Dry tap on bone marrow aspiration or grade 2-3 myelofibrosis.
- Pregnancy or breastfeeding status.
- Any other condition deemed inappropriate for study enrollment by the investigator.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Andet: Sonrotoclax plus Azacitidine in Newly-Diagnosed Higher-Risk Myelodysplastic Syndromes (MDS)
Patients with newly-diagnosed higher-risk MDS receive 28-day cycles of sonrotoclax (BGB-11417) plus azacitidine. Azacitidine 75 mg/m² is given subcutaneously or intravenously on Days 1-7. Sonrotoclax (RP2D 160 mg daily, Days 1-14 per cycle) undergoes 4-day dose ramp-up (20-40-80-160 mg) in Cycle 1, followed by full target dose in later cycles. |
Patients with newly-diagnosed higher-risk MDS receive 28-day cycles of sonrotoclax (BGB-11417) plus azacitidine. Azacitidine 75 mg/m² is given subcutaneously or intravenously on Days 1-7. Sonrotoclax (RP2D 160 mg daily, Days 1-14 per cycle) undergoes 4-day dose ramp-up (20-40-80-160 mg) in Cycle 1, followed by full target dose in later cycles. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Overall Response Rate (ORR)
Tidsramme: Up to 24 months
|
Description: The proportion of participants achieving objective response (CR or PR) per response criteria. Unit of Measure: Proportion |
Up to 24 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Complete Remission (CR) rate
Tidsramme: Up to 24 months
|
Description: The proportion of participants achieving complete remission per response criteria. Unit of Measure: Proportion |
Up to 24 months
|
|
Duration of Response (DOR)
Tidsramme: Up to 36 months
|
Description: Time from the first documented objective response to disease progression or death from any cause. Unit of Measure: Time (months) |
Up to 36 months
|
|
Progression-Free Survival (PFS)
Tidsramme: Up to 36 months
|
Outcome Measure: Progression-Free Survival (PFS) Description: Time from randomization to disease progression or death from any cause. Unit of Measure: Time (months) |
Up to 36 months
|
|
Overall Survival (OS)
Tidsramme: Up to 36 months
|
Outcome Measure: Overall Survival (OS) Description: Time from randomization to death from any cause. Unit of Measure: Time (months) |
Up to 36 months
|
|
Hematological/non-hematological adverse events
Tidsramme: From first study treatment dose to 30 days after last dose
|
Description: Incidence of hematological and non-hematological adverse events, graded per CTCAE. Unit of Measure: Incidence (proportion) |
From first study treatment dose to 30 days after last dose
|
Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2026-MDS-1
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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