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PBSS1113 in Combination With Azacitidine to Treat Patients With AML/MDS

12 de agosto de 2026 atualizado por: Chaser Therapeutics, Inc.

A Phase Ib/II, Open-Label, Dose-Escalation and Cohort Expansion Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PBSS1113 in Combination With Azacitidine in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome

Acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) are highly heterogeneous myeloid malignancies where few effective targeted therapies are available. While venetoclax has significantly advanced the treatment landscape, therapeutic resistance remains a critical challenge. Consequently, patients with relapsed or refractory (R/R) AML/MDS face a profound unmet medical need for novel therapeutic options. PBSS1113 has demonstrated robust anti-leukemic activity in both in vitro and in vivo models, alongside an acceptable safety profile in a Phase I study. This Phase Ib/II trial will evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of PBSS1113 in combination with azacitidine for treatment-naive unfit AML, R/R AML, and higher-risk MDS populations.

Visão geral do estudo

Status

Recrutamento

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Estimado)

29

Estágio

  • Fase 2
  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Zhejiang
      • Hangzhou, Zhejiang, China, 310003
        • Recrutamento
        • The First Affiliated Hospital of Zhejiang University school of medicine
        • Investigador principal:
          • Jie Jin, MD
        • Contato:
        • Investigador principal:
          • Hongyan Tong, MD

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Age and Gender: Age ≥ 18 years at the time of signing the informed consent form, male or female.
  • Disease Status: Must meet one of the following diagnostic criteria:
  • Relapsed or refractory (R/R) acute myeloid leukemia (AML).
  • Newly diagnosed AML in patients who are ineligible for intensive induction chemotherapy (including primary AML or secondary AML arising from myelodysplastic syndromes [MDS]).
  • Higher-risk MDS, defined per the Revised International Prognostic Scoring System (IPSS-R) as Intermediate risk (score > 3.5 points), High risk, or Very High risk. Prior therapy with hypomethylating agents (HMAs, e.g., decitabine or azacitidine) is permitted.
  • Performance Status: Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1, or 2.
  • Life Expectancy: Expected survival period ≥ 3 months.
  • Organ Function: Baseline organ function meeting the following laboratory criteria:
  • Hepatic: Total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN); aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 × ULN.
  • Renal: Serum creatinine ≤ 1.5 × ULN.
  • Coagulation: Activated partial thromboplastin time (APTT) ≤ 1.5 × ULN; prothrombin time (PT) ≤ 1.5 × ULN; International Normalized Ratio (INR) ≤ 1.5 × ULN.
  • Cardiac: Fridericia-corrected QT interval (QTcF) < 450 ms for males and < 470 ms for females.
  • Compliance: Able and willing to adhere to the study procedures, scheduling, and follow-up examinations outlined in the protocol.
  • Informed Consent: Capable of understanding and voluntarily providing written informed consent prior to the initiation of any trial-specific screening procedures.

Exclusion Criteria:

  • Leukemia Subtypes: Diagnosis of acute promyelocytic leukemia (APL), classified as AML-M3 per the French-American-British (FAB) criteria or APL with PML-RARA fusion gene per standard diagnostic classifications.
  • Concomitant Malignancies: Diagnosis of another active malignant tumor within the screening period, except for the target AML or MDS indications (as evaluated by the investigator).
  • Hyperleukocytosis: White blood cell (WBC) count > 25 × 10⁹/L during screening. Note: Hydroxyurea use is permitted to stabilize the WBC count below this threshold prior to first dose.
  • Contraception: Female patients of childbearing potential, male patients, and their partners who are unwilling to practice a medically accepted, highly effective method of contraception during the treatment period and for at least 6 months following the final dose of the investigational drug. Note: Women are considered postmenopausal if they have experienced at least 12 consecutive months of amenorrhea with no alternative pathological cause.
  • Prior/Concomitant Therapies:
  • Received radiotherapy, immunotherapy, hormonal therapy, targeted therapy, biologic therapy, traditional Chinese medicine indicated for oncology, chemotherapy, or any other investigational agent within 14 days prior to the first dose of the study drug.
  • Prior allogeneic hematopoietic stem cell transplantation (HSCT) with evidence of active graft-versus-host disease (GVHD), or requiring systemic immunosuppressive therapy for GVHD.
  • Use of strong CYP3A inhibitors or inducers within 14 days prior to the first dose of the study drug (unless on a stable, clinically justified regimen approved by the investigator).
  • Residual Toxicity: Unresolved toxicities from prior anti-cancer therapies that have not recovered to ≤ Grade 1 per CTCAE v5.0 (excluding alopecia and stable Grade 2 peripheral neuropathy, if applicable).
  • Surgery: Major surgical procedures or significant traumatic injuries within 28 days prior to the first dose of the study drug, or an anticipated requirement for major surgery during the trial.
  • Gastrointestinal Disorders: Difficulty swallowing or any clinically significant gastrointestinal disease or malabsorption syndrome that would significantly impair the oral absorption of the investigational drug.
  • Infections and Comorbidities:
  • Active, clinically significant, or poorly controlled fungal, bacterial, or viral infections at baseline.
  • Known human immunodeficiency virus (HIV) infection (anti-HIV positive).
  • Active hepatitis B virus (HBV; HBsAg positive and HBV DNA ≥ 2000 copies/mL or ≥ 500 IU/mL) or active hepatitis C virus (HCV; HCV antibody positive and HCV RNA positive).
  • Active syphilis infection.
  • Any severe, poorly controlled systemic comorbidities (e.g., unstable psychiatric, neurological, cardiovascular, respiratory, hepatic, or renal diseases).
  • Hypersensitivity: Known hypersensitivity or allergy to the investigational drug (PBSS1113), azacitidine, or any of their excipients.
  • Investigator Discretion: Any other clinical condition or social circumstance that, in the opinion of the investigator, would compromise patient safety or interfere with the scientific integrity of the study data.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição sequencial
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: PBSS1113
PBSS1113 in combination with azacitidine
PBSS1113 enteric tablet, 10/50 mg

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Composite Complete Remission (cCR) Rate in Patients with Acute Myeloid Leukemia (AML)
Prazo: Through study completion, an average of 1 year
The composite complete remission (cCR) rate is defined as the proportion of AML subjects who achieve a best overall response of complete remission (CR), complete remission with partial hematologic recovery (CRh), complete remission with incomplete hematologic recovery (CRi), or a morphological leukemia-free state (MLFS). The analysis will further evaluate the subset of patients achieving measurable residual disease (MRD) negativity within these categories (CRMRD-, CRhMRD-, or CRiMRD-).
Through study completion, an average of 1 year

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Overall Response Rate (ORR) in Patients with Myelodysplastic Syndrome (MDS)
Prazo: Through study completion, an average of 1 year
The overall response rate (ORR) is defined as the proportion of MDS subjects who achieve a best overall response according to the revised International Working Group (IWG) 2023 response criteria. This includes complete remission (CR), CR-equivalent (CRequiv), partial remission (PR), CR with limited count recovery (CRL), CR with partial hematologic recovery (CRh), or hematologic improvement (HI).
Through study completion, an average of 1 year

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

8 de setembro de 2025

Conclusão Primária (Estimado)

1 de setembro de 2027

Conclusão do estudo (Estimado)

1 de setembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

5 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

7 de agosto de 2026

Primeira postagem (Real)

12 de agosto de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

14 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

12 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Outros números de identificação do estudo

  • CT-102
  • CTR20253847 (Outro identificador: National Medical Products Administration, China)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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