Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Relacorilant and Nab-Paclitaxel in Recurrent or Metastatic Cervical Cancer (STELLA)

12 de agosto de 2026 atualizado por: ARCAGY/ GINECO GROUP

Second Line Therapy and Beyond With Relacorilant and Nab-Paclitaxel for Cervical Cancer With Loss of Benefit From Immune Checkpoint and Platinum Exposure

This phase II study will evaluate the efficacy and safety of relacorilant in combination with nab-paclitaxel in participants with recurrent or metastatic cervical cancer who have previously received platinum-based chemotherapy and anti-PD-1/PD-L1 therapy, if eligible.

STELLA is a prospective, open-label, single-arm study. Approximately 63 participants will receive relacorilant orally in combination with intravenous nab-paclitaxel in 28-day treatment cycles. Treatment will continue until disease progression, unacceptable toxicity, or another protocol-defined reason for discontinuation.

The primary objective of the study is to evaluate the objective response rate, defined as the proportion of participants with a complete or partial response as their best overall response according to RECIST version 1.1. Secondary objectives include evaluating duration of response, progression-free survival, overall survival, and the safety and tolerability of the combination.

Visão geral do estudo

Status

Ainda não está recrutando

Condições

Intervenção / Tratamento

Descrição detalhada

Recurrent or metastatic cervical cancer remains associated with poor outcomes after progression following platinum-based chemotherapy and immune checkpoint inhibitor therapy. Available subsequent treatment options are limited and are generally associated with modest clinical benefit.

Glucocorticoid receptor signaling may contribute to tumor cell survival, immune evasion, and resistance to anticancer therapy. Relacorilant is a selective glucocorticoid receptor modulator that may enhance sensitivity to taxane-based chemotherapy. The combination of relacorilant and nab-paclitaxel has demonstrated antitumor activity in previous clinical studies in other tumor types.

STELLA is a prospective, multicenter, open-label, single-arm phase II study designed to evaluate relacorilant in combination with nab-paclitaxel in participants with recurrent or metastatic cervical cancer previously exposed to platinum-based chemotherapy and immune checkpoint inhibition, if eligible. Approximately 63 participants are planned to be enrolled at approximately 22 sites.

Nab-paclitaxel will be administered intravenously at 80 mg/m² on Days 1, 8, and 15 of each 28-day cycle. Relacorilant will be administered orally at 150 mg once daily on the day before, the day of, and the day after each nab-paclitaxel administration, except that relacorilant will not be administered on the day before the first nab-paclitaxel dose at Cycle 1 Day 1.

The primary endpoint is objective response rate according to RECIST version 1.1, defined as the proportion of participants achieving a complete response or partial response as their best overall response during the study. The study will also assess duration of response, progression-free survival, overall survival, safety, and exploratory translational objectives.

Tipo de estudo

Intervencional

Inscrição (Estimado)

63

Estágio

  • Fase 2

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: Sidonie ADAM
  • Número de telefone: +33 1 84 85 20 18
  • E-mail: sadam@arcagy.org

Locais de estudo

      • Lyon, França
        • Centre Léon Bérard
        • Contato:
          • Isabelle RAY-COQUARD, MD, PhD
        • Investigador principal:
          • Isabelle RAY-COQUARD, MD,PhD
      • Paris, França
        • Groupe Hospitalier Diaconesses Croix Saint-Simon
        • Investigador principal:
          • Antoine ANGELERGUES, MD
        • Contato:
          • Antoine Angelergues, 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:

  • Histologically confirmed diagnosis of squamous cell carcinoma, adenosquamous carcinoma, or adenocarcinoma of the cervix.
  • Recurrent or metastatic cervical cancer:
  • Has progressed on or after treatment with 1 prior line of systemic platinum doublet chemotherapy, with or without bevacizumab. Prior chemoradiotherapy in the Locally Advanced Cervical Cancer (LACC) setting is not considered a line of treatment.
  • Has received anti-PD-1/anti-PD-L1 therapy as part of a prior cervical cancer treatment regimen, if eligible.
  • Has received no more than 3 prior systemic regimens for advanced disease, with no more than one line of single-agent chemotherapy, and/or no more than one antibody-drug conjugate (ADC) therapy.
  • Has received no prior treatment with weekly paclitaxel, other than a front-line combination treatment as part of a platinum doublet regimen.
  • Has measurable disease per RECIST v1.1, as assessed by the investigator. Lesions situated in a previously irradiated area are considered measurable if radiographic progression has been demonstrated in such lesions.
  • Has provided documented informed consent.
  • Is assigned female sex at birth and is at least 18 years of age at the time of providing informed consent.
  • Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 within 7 days before inclusion.
  • Has consented to provide available formalin-fixed paraffin-embedded (FFPE) tumor tissue from a core/excisional biopsy or surgical resection specimen. If unavailable, the most representative FFPE tumor block of the disease should be provided.
  • Adverse events due to previous anticancer therapies must have recovered to Grade ≤1 or baseline, except alopecia or vitiligo. Participants with endocrine-related adverse events who are adequately treated with hormone replacement therapy are eligible.
  • Participants with HIV infection must have well-controlled HIV on antiretroviral therapy (ART), defined as:
  • CD4+ T-cell count ≥350 cells/mm³ at screening.
  • Confirmed HIV RNA below 50 copies/mL or below the lower limit of quantification for at least 12 weeks before screening.
  • No AIDS-defining opportunistic infection within the previous 12 months.
  • Stable ART regimen without changes in drugs or dose modification for at least 4 weeks before inclusion, with agreement to continue ART throughout the study. The ART regimen must not contain strong CYP3A4 inducers or CYP3A substrates that cannot be dose-adjusted when coadministered with strong CYP3A inhibitors.
  • Participants who are HBsAg positive are eligible if they have received HBV antiviral therapy for at least 4 weeks and have undetectable HBV viral load prior to inclusion.
  • Has adequate organ function:
  • Absolute neutrophil count ≥1,500 cells/mm³ without G-CSF support within 2 weeks before screening laboratory sample collection.
  • Platelet count ≥100,000/mm³ without transfusion within 2 weeks before screening laboratory sample collection.
  • Hemoglobin ≥9 g/dL without transfusion within 2 weeks before screening laboratory sample collection.
  • AST and ALT ≤2.5 × upper limit of normal (ULN), or ≤5 × ULN in the presence of liver metastases.
  • Total bilirubin ≤1.5 × ULN, or ≤3 × ULN for participants with Gilbert's syndrome.
  • Albumin ≥2.5 g/dL.
  • Calculated creatinine clearance ≥30 mL/min, with full recovery from any episode of acute renal failure.
  • Participants of childbearing potential must have a negative pregnancy test and agree to use highly effective contraception; hormonal contraceptives are not allowed.
  • Is affiliated with a social insurance regimen.
  • Is willing and able to comply with the protocol for the duration of the study, including treatment, scheduled visits, examinations, and follow-up.

Exclusion Criteria:

  • Grade ≥2 peripheral neuropathy.
  • Active inflammatory bowel disease requiring immunosuppressive medication or previous history of inflammatory bowel disease, including Crohn's disease, ulcerative colitis, or chronic diarrhea.
  • Clinically relevant and reversible toxicity from prior systemic anticancer therapies or radiotherapy that has not resolved to Grade ≤1 before enrollment, except alopecia, hearing loss, vitiligo, and endocrinopathy managed with replacement therapy.
  • Surgery within 4 weeks prior to enrollment or anticipated requirement for a surgical procedure during the study. Participants must have adequately recovered from toxicity and/or complications of prior major surgery.
  • Has received any of the following before enrollment:
  • Chemotherapy, immunotherapy, investigational agent, or other treatment for the disease under study within 5 half-lives of the prior therapy, or 28 days if 5 half-lives is longer than 28 days, before the first dose of study treatment.
  • Radiotherapy not completed at least 2 weeks before the first dose of study treatment.
  • Systemic, inhaled, or prescription-strength topical corticosteroids within a period equivalent to 5 half-lives of the corticosteroid before the first dose.
  • Wide-field radiation therapy to more than 25% of marrow-bearing areas.
  • Requires chronic or frequently used systemic corticosteroids for medical conditions or illnesses.
  • History of severe hypersensitivity or severe reaction to any study treatment.
  • Has received prior treatment with mifepristone or another glucocorticoid receptor modulator as part of a treatment regimen for cervical cancer.
  • Is pregnant, breastfeeding, or planning to conceive during the projected duration of the study through at least 6 months after the last dose of study treatment.
  • Has clinically significant uncontrolled condition(s) that, in the investigator's opinion, may confound study results or interfere with participant safety or participation, including but not limited to:
  • Unstable angina.
  • Myocardial infarction within 6 months before the first dose.
  • New York Heart Association Class II or greater congestive heart failure.
  • Serious cardiac arrhythmia requiring medication or prolongation of QTcF.
  • Severe or advancing cirrhosis.
  • Active infectious disease requiring intravenous therapy within 2 weeks before the first dose.
  • Gastric-outlet obstruction.
  • Acute renal failure that has not recovered to baseline renal function.
  • Known psychiatric disorder that would interfere with study compliance.
  • Current uncontrolled chronic or acute infection with HIV, hepatitis C virus, or hepatitis B virus.
  • Untreated, symptomatic, or corticosteroid-dependent central nervous system metastases.
  • History of another malignancy within 3 years before enrollment, except tumors with negligible risk of metastasis or death, such as adequately controlled basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast.
  • Is taking a prohibited concomitant medication specified in the protocol.
  • Is receiving concurrent treatment in another investigational treatment study for cervical cancer.
  • Has received a live vaccine within 30 days before study treatment. Injectable seasonal influenza vaccines are generally inactivated and are permitted; intranasal live attenuated influenza vaccines are prohibited.
  • Is deprived of liberty, under guardianship or curatorship, or otherwise meets the legal definition of a vulnerable person under Regulation (EU) No. 536/2014.

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 de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Relacorilant and Nab-Paclitaxel
Participants will receive relacorilant 150 mg orally in combination with nab-paclitaxel 80 mg/m² administered intravenously on Days 1, 8, and 15 of each 28-day cycle. Relacorilant will be administered once daily on the day before, the day of, and the day after each nab-paclitaxel infusion, except that relacorilant will not be administered on the day before the first nab-paclitaxel infusion at Cycle 1 Day 1. Treatment will continue until disease progression, unacceptable toxicity, or another protocol-defined reason for discontinuation.
Relacorilant 150 mg will be administered orally once daily on the day before, the day of, and the day after each nab-paclitaxel administration. Relacorilant will not be administered on the day before the first nab-paclitaxel dose at Cycle 1 Day 1. Treatment is administered in 28-day cycles.
Nab-paclitaxel 80 mg/m² will be administered intravenously on Days 1, 8, and 15 of each 28-day treatment cycle.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Objective Response Rate (ORR) According to RECIST v1.1
Prazo: From the date of first study treatment until documented disease progression, assessed up to 48 months.
Objective Response Rate (ORR) is defined as the proportion of participants with a Complete Response (CR) or Partial Response (PR) as their best overall response according to RECIST version 1.1, based on investigator assessment. Participants with early death, clinical progression, or treatment discontinuation due to toxicity before any tumor assessment will be considered treatment failures. Tumor assessments performed after initiation of subsequent anticancer therapy will not contribute to the ORR assessment.
From the date of first study treatment until documented disease progression, assessed up to 48 months.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Duration of Response (DoR)
Prazo: From the date of first documented CR or PR until documented disease progression or death from any cause, whichever occurs first, assessed up to 48 months.
Duration of Response (DoR) is defined as the time from the date of first documented Complete Response (CR) or Partial Response (PR) until the date of documented disease progression according to RECIST version 1.1, as assessed by the investigator, or death from any cause.
From the date of first documented CR or PR until documented disease progression or death from any cause, whichever occurs first, assessed up to 48 months.
Progression-Free Survival (PFS)
Prazo: From the date of first study treatment until documented disease progression or death from any cause, whichever occurs first, assessed up to 48 months.
Progression-Free Survival (PFS) is defined as the time from the date of first study treatment until the date of documented disease progression according to RECIST version 1.1, as assessed by the investigator, or death from any cause.
From the date of first study treatment until documented disease progression or death from any cause, whichever occurs first, assessed up to 48 months.
Overall Survival (OS)
Prazo: From the date of first study treatment until death from any cause, assessed up to 48 months.
Overall Survival (OS) is defined as the time from the date of first study treatment until death from any cause.
From the date of first study treatment until death from any cause, assessed up to 48 months.
Incidence and Severity of Adverse Events
Prazo: From the first dose of study treatment until 30 days after the last dose of study treatment or until initiation of alternative cancer therapy, whichever occurs first.
Safety will be assessed by the incidence and severity of adverse events, classified by maximum grade, System Organ Class (SOC), and Preferred Term (PT), according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 6.0.
From the first dose of study treatment until 30 days after the last dose of study treatment or until initiation of alternative cancer therapy, whichever occurs first.

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Antoine ANGELERGUES, MD, Groupe Hospitalier Diaconesses Croix Saint-Simon
  • Cadeira de estudo: Isabelle RAY-COQUARD, MD, PhD, Centre Léon Bérard

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 outubro de 2026

Conclusão Primária (Estimado)

1 de dezembro de 2030

Conclusão do estudo (Estimado)

1 de dezembro de 2030

Datas de inscrição no estudo

Enviado pela primeira vez

6 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

12 de agosto de 2026

Primeira postagem (Real)

13 de agosto de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

13 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

Outros números de identificação do estudo

  • GINECO-CE201b
  • 2026-527245-22-00 (Ctis)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

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

produto fabricado e exportado 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 .