- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07559929
A Study of DXC006 With Immune Checkpoint Inhibitors or Platinum for Small Cell Lung Cancer.
27 de maio de 2026 atualizado por: Hangzhou DAC Biotechnology Co., Ltd.
A Phase Ib/II Study to Evaluate the Safety and Efficacy of DXC006 for Injection Combined With Immune Checkpoint Inhibitors or Platinum-Based Agents in Patients With Small Cell Lung Cancer.
This is a Phase Ib/II, open-label clinical study designed to evaluate the safety, tolerability, preliminary anti-tumor activity, recommended Phase 2 dose (RP2D), pharmacokinetic (PK) characteristics, and immunogenicity of DXC006 in combination with an immune checkpoint inhibitor (ICI) or platinum-based chemotherapy in patients with small cell lung cancer (SCLC).
Visão geral do estudo
Status
Ainda não está recrutando
Condições
Intervenção / Tratamento
Tipo de estudo
Intervencional
Inscrição (Estimado)
200
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
- Nome: Li Zhang, Doctoral degree
- Número de telefone: +86-020-87343565
- E-mail: zhangli@sysucc.org.cn
Locais de estudo
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Guangdong
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Guangzhou, Guangdong, China, 510060
- Sun Yat-sen University Cancer Center
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Contato:
- Li Zhang, Doctoral degree
- Número de telefone: +86-020-87343565
- E-mail: zhangli@sysucc.org.cn
-
-
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:
- Voluntarily signed informed consent and willingness to comply with the protocol requirements.
- Male or female.
- Age ≥18 years and ≤75 years.
- Life expectancy ≥3 months.
- Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2.
- Histologically or cytologically confirmed small cell lung cancer (SCLC).
- Toxicity from prior anti-tumor therapy has resolved to ≤ Grade 1 as defined by NCI-CTCAE version 6.0 (except alopecia); peripheral neuropathy must have completely resolved.
- Adequate hepatic, renal, coagulation, and cardiac function.
- The participant and their spouse agree to use effective barrier or pharmacologic contraception (excluding rhythm method) from the time of signing the informed consent until 6 months after the last dose of study treatment.
Exclusion Criteria:
- Histologically or cytologically confirmed combined SCLC, NSCLC, sarcomatoid carcinoma, or large cell neuroendocrine carcinoma.
- Within 14 days prior to the first dose: underwent plasmapheresis; received systemic corticosteroid therapy at a daily dose >10 mg prednisone or equivalent (or equivalent anti-inflammatory activity) for more than 3 consecutive days (short-term use for prevention of contrast media allergy is permitted).
- Prior allogeneic hematopoietic stem cell transplantation (HSCT) or history of solid organ transplantation.
- Prior treatment with CD56-targeted therapy.
- Symptomatic brain metastases or leptomeningeal metastases.
- History of severe or life-threatening immune-related adverse events or infusion-related reactions (including permanent discontinuation of immuno-oncology therapy due to intolerance).
- Active autoimmune disease or immunodeficiency, or a history of such conditions.
- Evidence of significant cardiovascular risk.
- Dyspnea or current requirement for continuous supplemental oxygen therapy, or current active pneumonitis or interstitial lung disease (except mild cases as determined by the investigator).
- History of other primary malignancies, with the exception of malignancies that have been cured and have a very low risk of recurrence within 5 years, such as basal cell carcinoma or squamous cell carcinoma of the skin, or carcinoma in situ of the cervix or breast.
- Severe non-healing wound, ulcer, or bone fracture; or major surgery within 28 days prior to dosing, or anticipated major surgery during the study period.
- History of hypersensitivity to any component or excipient of DXC006, immune checkpoint inhibitors, or platinum-based chemotherapy.
- Active hepatitis B (HBV-DNA above the upper limit of normal at the central laboratory or >1000 copies/mL); hepatitis C infection (positive hepatitis C antibody or positive HCV RNA PCR result).
- Known positive serology for human immunodeficiency virus (HIV); active syphilis (patients with positive syphilis antibody only are eligible); potential active pulmonary tuberculosis (chest imaging within 3 months prior to the first dose suggestive of active tuberculosis infection).
- Active bleeding within 30 days prior to screening, or risk of major gastrointestinal bleeding or hemoptysis as determined by the investigator; or hereditary bleeding tendency, coagulopathy, or bleeding symptoms requiring other medical intervention.
- Severe arterial or venous thromboembolic events within 6 months prior to study drug administration, such as cerebrovascular accident (including transient ischemic attack), deep vein thrombosis, or pulmonary embolism.
- Positive serum pregnancy test or currently breastfeeding female participants.
- Active infection requiring medical therapy (CTCAE Grade ≥2); uncontrollable pleural effusion, ascites, or pericardial effusion requiring repeated drainage.
- Administration of live attenuated vaccines within 28 days prior to the first dose.
- Other conditions that, in the judgment of the investigator, may affect the patient's participation in the study.
- Poor general condition, such as requirement for mechanical ventilation and/or intravenous catecholamine infusion, and/or severe neurological impairment, coma, and/or quadriplegia with complete loss of communication ability (deafness, blindness, aphasia); uncontrolled seizures; other psychiatric disorders that may affect study participation.
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: Não randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: DXC006 + ICI
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Participants receive DXC006 intravenously on Day 1 every 3 weeks.
Participants receive Toripalimab intravenously on Day 1 every 3 weeks.
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Experimental: DXC006 + Platinum(Carboplatin )
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Participants receive DXC006 intravenously on Day 1 every 3 weeks.
Participants receive Carboplatin intravenously on Day 1 every 3 weeks (up to 6 cycles).
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Experimental: DXC006 + Platinum(Cisplatin )
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Participants receive DXC006 intravenously on Day 1 every 3 weeks.
Participants receive Cisplatin intravenously on Day 1 every 3 weeks (up to 6 cycles).
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Progression Free Survival (PFS)
Prazo: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
|
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
|
|
6-month progression-free survival rate
Prazo: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months.
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From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months.
|
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Recommended Phase 2 Dose (RP2D)
Prazo: Final RP2D confirmation upon completion of the Phase Ib (up to 12 months).
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Final RP2D confirmation upon completion of the Phase Ib (up to 12 months).
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Measurement of objective response rate (ORR) per RECIST 1.1
Prazo: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
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From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
|
|
Measurement of disease control rate (DCR)
Prazo: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
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From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
|
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Incidence of Adverse Events (AEs)
Prazo: After first infusion of study drug, through study completion an average of 2 year.
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After first infusion of study drug, through study completion an average of 2 year.
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Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Maximum observed serum or plasma concentration (Cmax)
Prazo: Through study completion an average of 1 year.
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Through study completion an average of 1 year.
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Maximum serum drug time(Tmax)
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
|
Apparent volume of distribution(Vd)
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Volume of distribution at steady state (Vss)
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Terminal phase elimination half life (t½)
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Area under the serum or plasma concentration time curve from 0 to the last measurable point (AUC0-t).
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Area under the serum or plasma concentration time curve from 0 to infinity (AUC0-inf)
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Clearance (CL)
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Ctrough
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Anti-drug antibodies (ADA)
Prazo: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
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Overall Survival (OS)
Prazo: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
|
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
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Duration of response (DOR)
Prazo: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
|
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
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 (Estimado)
1 de junho de 2026
Conclusão Primária (Estimado)
1 de junho de 2028
Conclusão do estudo (Estimado)
30 de dezembro de 2030
Datas de inscrição no estudo
Enviado pela primeira vez
24 de abril de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
24 de abril de 2026
Primeira postagem (Real)
30 de abril de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
29 de maio de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
27 de maio de 2026
Última verificação
1 de março de 2026
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Neoplasias por local
- Neoplasias
- Doenças Respiratórias
- Doenças pulmonares
- Neoplasias do Trato Respiratório
- Neoplasias Torácicas
- Neoplasias Pulmonares
- Carcinoma Broncogênico
- Neoplasias Brônquicas
- Carcinoma pulmonar de pequenas células
- Produtos químicos orgânicos
- Produtos químicos inorgânicos
- Compostos de cloro
- Compostos de nitrogênio
- Complexos de coordenação
- Compostos de platina
- Carboplatina
- Cisplatina
- Toripalimab
Outros números de identificação do estudo
- DXC006-002
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 .