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A Phase II Study of Nab-Paclitaxel Combined With Retlirafusp Alfa and Apatinib in Patients With Advanced Mucosal Melanoma

8 novembre 2026 mis à jour par: xizhi wen, Sun Yat-sen University

A Prospective, Single-Arm, Phase II Study of Nab-Paclitaxel Combined With Retlirafusp Alfa Injection and Apatinib Mesylate for Advanced Mucosal Melanoma

This is a prospective, single-arm, open-label Phase II clinical study. The main purpose of this study is to evaluate the effectiveness of nab-paclitaxel combined with retlirafusp alfa injection and apatinib mesylate in patients with advanced mucosal melanoma.

Participants will receive treatment with nab-paclitaxel combined with retlirafusp alfa injection and apatinib mesylate. Each treatment cycle lasts 3 weeks, and participants will receive a total of 6 cycles. Participants whose disease does not progress after the initial treatment will continue maintenance therapy with apatinib mesylate combined with retlirafusp alfa injection until their disease progresses or they experience intolerable side effects.

After enrollment, participants will undergo safety visits before each dose on Day 1 and Day 21 of each treatment cycle. Tumor imaging assessments will be performed before treatment and after every 2 to 4 cycles of treatment. Clinical response will be evaluated by radiologists according to the RECIST 1.1 criteria.

Researchers will monitor participants for any adverse events throughout the study and will grade the severity of these events according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. After treatment is completed, participants will be followed for 12 weeks for safety monitoring, and long-term survival follow-up will continue.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

27

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

  • Nom: Xiaoshi Zhang, phD

Lieux d'étude

    • Guangdong
      • Guangzhou, Guangdong, Chine
        • Recrutement
        • Sun yat-sen uniersity
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Age ≥ 18 years.

  2. Histopathologically confirmed unresectable or metastatic mucosal melanoma.

  3. Subjects must provide 5 paraffin-embedded tissue sections obtained prior to treatment for immune microenvironment (immune infiltration) scoring.

  4. The Eastern Cooperative Oncology Group (ECOG) scoring system in the United States has a score range of 0-1.

  5. No prior systemic therapy. Patients who developed recurrence or metastasis more than 6 months after discontinuation of adjuvant therapy are excluded from this criterion (i.e., such patients are eligible).

  6. Presence of at least one measurable lesion according to RECIST 1.1 criteria.

  7. No history of immunosuppressive drug use within 6 months prior to enrollment.

  8. Adequate hematologic and organ function, meeting the following laboratory criteria:

    i. Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L; ii. Platelet count ≥ 100 × 10⁹/L; iii. Hemoglobin > 9.0 g/dL; iv. Serum creatinine ≤ 1.5 × ULN, or creatinine clearance (CrCl) ≥ 40 mL/min; v. AST/ALT ≤ 3 × ULN; vi. Total bilirubin ≤ 1.5 × ULN.

  9. No active bleeding.

  10. Urine protein ≤ 1+ or < 1 g/24h.

  11. Women of childbearing potential must have a negative serum or urine pregnancy test and agree to use adequate contraception (barrier method or oral contraceptives) during the study.

Exclusion Criteria:

  1. Patients with active autoimmune disease. Note: Patients with vitiligo, type I diabetes mellitus, or hypothyroidism due to Hashimoto's thyroiditis requiring only hormone replacement therapy may be enrolled if there is no obvious evidence of recurrence.
  2. Patients requiring systemic corticosteroid therapy (> 10 mg prednisone [or equivalent] per day) or other immunosuppressive agents within 14 days after enrollment. Note: Inhaled or topical corticosteroids, or adrenal hormone replacement therapy (> 10 mg prednisone [or equivalent] per day) are acceptable for patients without obvious autoimmune disease.
  3. Patients with concurrent other malignancy requiring anti-tumor therapy cannot be enrolled in this study. However, if the malignancy has achieved complete remission for two years or more, and no additional anti-tumor therapy is required during the study period, enrollment may be considered.
  4. Patients who, in the investigator's judgment, are medically, psychologically, or physiologically unable to complete this study or to understand the patient information.
  5. Prior treatment with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CTLA-4, anti-TGF-β, or other agents targeting T-cell co-stimulatory or immune regulatory pathways.
  6. Prior treatment with taxanes, platinum-based agents, or anti-angiogenic agents.
  7. Presence of untreated CNS metastases, or CNS metastases requiring corticosteroids for edema control.
  8. Tumor invasion of major blood vessels (e.g., carotid artery, aorta), concurrent active ulcer, or history of gastrointestinal bleeding.
  9. History of myocardial infarction or stroke within the past 6 months.
  10. Positive HIV test or confirmed diagnosis of acquired immunodeficiency syndrome (AIDS).
  11. Uncontrolled hypertension, commonly defined as: systolic blood pressure ≥ 140 mmHg or diastolic blood pressure ≥ 90 mmHg despite optimized antihypertensive therapy, or requiring ≥ 2 antihypertensive agents without achieving target.
  12. Cardiac arrhythmias requiring pharmacological or device intervention, affecting hemodynamic stability, or posing a risk of sudden death, including but not limited to uncontrolled rapid atrial fibrillation, ventricular tachycardia, atrioventricular block, and QTc ≥ 500 ms.
  13. Uncontrolled heart failure, defined as NYHA class III-IV, or persistent significant symptoms despite optimized therapy, or recent need for hospitalization or intravenous therapy, or significantly reduced left ventricular ejection fraction (e.g., < 40-50%).
  14. Patients with a history of severe (≥ G3) immune-related adverse events (irAEs) involving major organs, such as immune-mediated hepatitis, pneumonitis, myocarditis, colitis, or central nervous system toxicity.
  15. Presence of unhealed wounds.
  16. Allergy to the study drug or its components.
  17. Pregnant or lactating women.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Assigned Interventions

Drug: Nab-paclitaxel Injection Nab-paclitaxel 200 mg/m² IV infusion Q3W

Drug: Retlirafusp Alfa Injection Retlirafusp Alfa 1 diluted in 250 mL normal saline IV, administered 30 minutes before chemotherapy, Q3W

Drug: Apatinib Mesylate Tablet Apatinib Mesylate 250 mg PO QD

Regimen: Nab-paclitaxel + Retlirafusp Alfa + Apatinib Mesylate, Q3W × 6 cycles (combination phase); maintenance: Apatinib Mesylate + Retlirafusp Alfa until disease progression or unacceptable toxicity

Drug: Nab-paclitaxel Injection Nab-paclitaxel 200 mg/m² IV infusion Q3W

Drug: Retlirafusp Alfa Injection Retlirafusp Alfa diluted in 250 mL normal saline IV, administered 30 minutes before chemotherapy, Q3W

Drug: Apatinib Mesylate Tablet Apatinib Mesylate 250 mg PO QD

Regimen: Nab-paclitaxel + Retlirafusp Alfa + Apatinib Mesylate, Q3W × 6 cycles (combination phase); maintenance: Apatinib Mesylate + SHR-1701 until disease progression or unacceptable toxicit

Autres noms:
  • Nab-paclitaxel Injection
  • Apatinib Mesylate Tablet

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Objective Response Rate (ORR: CR+PR)
Délai: up to 18 weeks

defined as the best overall response of complete remission or partial remission

up to 18 weeks

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
AEs+SAEs
Délai: from the first drug administration to within 30 days for the last SHR-1701 dose

Adverse Events and Serious Adverse Events

from the first drug administration to within 30 days for the last SHR-1701 dose
overall survival(OS)
Délai: Assessed until 12 months after the first dose of the last enrolled patient, estimated up to 5 years

defined as the time from enrollment to death due to any cause

Assessed until 12 months after the first dose of the last enrolled patient, estimated up to 5 years
progress-free survival(RFS)
Délai: Assessed until 12 months after the first dose of the last enrolled patient, estimated up to 5 years

Defined as the time from enrollment to the first documented disease progression, death from any cause, or the last date on which the patient was recorded as being free of disease progression.

Assessed until 12 months after the first dose of the last enrolled patient, estimated up to 5 years

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

29 septembre 2026

Achèvement primaire (Estimé)

31 décembre 2029

Achèvement de l'étude (Estimé)

31 décembre 2029

Dates d'inscription aux études

Première soumission

8 novembre 2026

Première soumission répondant aux critères de contrôle qualité

8 novembre 2026

Première publication (Réel)

13 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

8 novembre 2026

Dernière vérification

1 novembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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