- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07559929
A Study of DXC006 With Immune Checkpoint Inhibitors or Platinum for Small Cell Lung Cancer.
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).
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Li Zhang, Doctoral degree
- Numéro de téléphone: +86-020-87343565
- E-mail: zhangli@sysucc.org.cn
Lieux d'étude
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Guangdong
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Guangzhou, Guangdong, Chine, 510060
- Recrutement
- Sun Yat-sen University Cancer Center
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Contact:
- Li Zhang, Doctoral degree
- Numéro de téléphone: +86-020-87343565
- E-mail: zhangli@sysucc.org.cn
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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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Expérimental: 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). |
|
Expérimental: 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). |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Progression Free Survival (PFS)
Délai: 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
Délai: 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.
|
|
Recommended Phase 2 Dose (RP2D)
Délai: 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).
|
|
Measurement of objective response rate (ORR) per RECIST 1.1
Délai: 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)
Délai: 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)
Délai: After first infusion of study drug, through study completion an average of 2 year.
|
After first infusion of study drug, through study completion an average of 2 year.
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Maximum observed serum or plasma concentration (Cmax)
Délai: 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)
Délai: Through study completion an average of 1 year.
|
Through study completion an average of 1 year.
|
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Apparent volume of distribution(Vd)
Délai: Through study completion an average of 1 year.
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Through study completion an average of 1 year.
|
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Volume of distribution at steady state (Vss)
Délai: Through study completion an average of 1 year.
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Through study completion an average of 1 year.
|
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Terminal phase elimination half life (t½)
Délai: 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).
Délai: 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)
Délai: Through study completion an average of 1 year.
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Through study completion an average of 1 year.
|
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Clearance (CL)
Délai: Through study completion an average of 1 year.
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Through study completion an average of 1 year.
|
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Ctrough
Délai: Through study completion an average of 1 year.
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Through study completion an average of 1 year.
|
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Anti-drug antibodies (ADA)
Délai: Through study completion an average of 1 year.
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Through study completion an average of 1 year.
|
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Overall Survival (OS)
Délai: 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)
Délai: 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.
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs par site
- Tumeurs
- Maladies des voies respiratoires
- Maladies pulmonaires
- Tumeurs des voies respiratoires
- Tumeurs thoraciques
- Tumeurs pulmonaires
- Carcinome bronchique
- Tumeurs bronchiques
- Carcinome pulmonaire à petites cellules
- Produits chimiques organiques
- Produits chimiques inorganiques
- Composés de chlore
- Composés d'azote
- Complexes de coordination
- Composés en platine
- Carboplatine
- Cisplatine
- toripalimab
Autres numéros d'identification d'étude
- DXC006-002
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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