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Lo studio clinico NCT06561555 per Mammary or Extramammary Paget's Disease è in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui. | ||
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Università FudanA Study on the Efficacy of Disitamab Vedotin in Advanced HER2-positive Paget's Disease. Fase II 36
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La sperimentazione clinica NCT06561555 è uno studio interventistico di Fase II volto a esaminare il trattamento per Mammary or Extramammary Paget's Disease, attualmente in arruolamento. Avviato il 15 agosto 2024, prevede di arruolare 36 partecipanti. Sotto la guida di l'Università Fudan, dovrebbe concludersi entro il 15 agosto 2027. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 17 dicembre 2024.
Sommario breve
This study is a single-center, phase II clinical trial. Patients with HER2-positive advanced breast and extramammary Paget's disease who met the eligibility criteria were enrolled after signing an informed consent form. All patients received treatment with 2mg/kg of trastuzumab deruxtecan intravenous infusion every 3 weeks until disease progression. Follow-up was conducted until disease progression, withdrawal of inf...Mostra di più
Titolo ufficiale
A Phase II Clinical Study on the Efficacy of Disitamab Vedotin in Advanced HER2-positive Paget's Disease.
Patologie
Mammary or Extramammary Paget's DiseaseAltri ID dello studio
- PAGET-SC-02
Numero NCT
Data di inizio (effettiva)
2024-08-15
Ultimo aggiornamento pubblicato
2024-12-17
Data di completamento (stimata)
2027-08-15
Arruolamento (previsto)
36
Tipo di studio
Interventistico
FASE
Fase II
Stato
In arruolamento
Scopo principale
Trattamento
Allocazione
N.D.
Modello di intervento
A gruppo singolo
Mascheramento
Nessuno (studio in aperto)
Bracci / Interventi
| Gruppo/Braccio di partecipanti | Intervento/Trattamento |
|---|---|
SperimentaleStudy group | RC48 RC48 at a dosage of 2mg/kg administered intravenously every 3 weeks (ivgtt q3w) is continued until disease progression, with the allowance for treatment discontinuation due to disease progression, death, intolerable toxicity, withdrawal of informed consent, initiation of new antineoplastic therapy, or other reasons specified in the protocol, with the earliest occurring event taking precedence. Alternatively, the stud...Mostra di più |
Esito primario
Esito secondario
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Objective Response Rate | ORR includes two categories:
Complete Response (CR): All target lesions in the patient have completely disappeared, and no new lesions have appeared for a certain time.
Partial Response (PR): The tumor in the patient has reduced in size by at least 30%, and this reduction has been maintained for a certain period. | every 6 weeks,up to 24 weeks |
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Progression free survival | Progression-Free Survival (PFS) is a clinical endpoint used primarily in oncology to measure the effectiveness of a treatment in delaying the progression of a disease. It is defined as the length of time during which a patient's disease does not get worse after starting a treatment. PFS takes into account the time from the start of treatment until the first occurrence of disease progression, or the patient's death if it occurs before progression. | through study completion, an average of 2 year |
advance events | advance events | through study completion, an average of 2 year |
Assistente alla partecipazione
Criteri di eleggibilità
Età idonea
Adulto, Adulto anziano
Età minima
18 Years
Sessi idonei
Tutti
- Voluntarily sign the informed consent form and comply with the requirements of the protocol.
- Age ≥ 18 years old.
- Confirmed diagnosis by histological examination and/or cytological examination, combined with imaging or ultrasound assessment for mammary and extramammary Paget's disease; pathologically confirmed as HER2 positive, i.e., immunohistochemical test HER2 ≥ 1+.
- ECOG score: 0 to 1.
- At least one measurable lesion (according to the RECIST criteria, non-nodal lesions with a longest diameter on CT scan ≥10 mm, and nodal lesions with a shortest diameter on CT scan ≥15 mm); or skin lesions that can be evaluated according to the WHO criteria.
- Adequate organ function: Blood routine: Absolute Neutrophil Count (ANC) ≥1.5×10^9/L, Platelet (PLT) ≥70×10^9/L, Hemoglobin (HGB) ≥80g/L; Liver function: Total Bilirubin (TBIL) ≤1.5×Upper Limit of Normal Value (ULN); Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) ≤3×ULN; Serum Albumin ≥28 g/L; Alkaline Phosphatase (ALP) ≤5×ULN; If the subject has received routine liver protection treatment and meets the above standards, and is stable for at least one week after assessment by the researcher, they may be enrolled; Renal function: Serum Creatinine (Cr) ≤1.5×ULN, or Creatinine Clearance ≥50 mL/min (using the standard Cockcroft-Gault formula): Coagulation function: International Normalized Ratio (INR) ≤1.5 / Prothrombin Time (PT) ≤1.5×ULN, Activated Partial Thromboplastin Time (aPTT) ≤1.5×ULN; If the subject is receiving anticoagulant therapy, as long as PT and INR are within the range specified for the anticoagulant medication, it is acceptable.
- Estimated life expectancy ≥3 months.
- Have a history of immunodeficiency, including HIV positive or other acquired or congenital immunodeficiency diseases, or a history of organ transplantation;
- Have had active autoimmune diseases within 2 years prior to the start of the study treatment that required systemic treatment (such as the use of disease-modifying drugs, corticosteroids, or immunosuppressants), except for replacement therapies (e.g., thyroid hormone, insulin, or physiological corticosteroids for adrenal or pituitary insufficiency); currently receiving systemic glucocorticoid therapy or any other form of immunosuppressive therapy. The dose is >10mg/day of prednisone or other equivalent hormones, and it is within 2 weeks of the first administration and still in use;
- Have a history of active tuberculosis;
- Have uncontrollable, recurrent drainage of ascites, pericardial effusion, or pleural effusion;
- Have undergone major organ transplantation;
- Received major surgical treatment, incisional biopsy, or significant traumatic injury within 28 days prior to the start of the study treatment; or have chronic non-healing wounds or fractures;
- Have a history of live attenuated vaccine administration within 14 days prior to the start of the study treatment or plan to receive live attenuated vaccine vaccination during the study period;
- Have had a severe hypersensitivity reaction after the use of monoclonal antibodies; known allergy to the active ingredients or excipients of this study drug;
- Within 4 weeks prior to the start of the study, are participating in or have participated in other clinical studies;
- Have a history of severe allergies;
- Have a risk of bleeding, or coagulation dysfunction, or are currently receiving -thrombolytic therapy;
- Have a history of substance abuse and are unable to quit or have mental disorders;
- According to the investigator's judgment, there are concomitant diseases that seriously endanger the safety of the subject or affect the completion of the study, or there are other reasons deemed unsuitable for enrollment by the investigator.
Università Fudan829 studi clinici attivi da esplorareParte responsabile dello studio
Hongxia Wang, Investigatore principale, Chief of Internal Medicine, Fudan University
Contatti principali dello studio
Contatto: wang hongxia, PHD, 021-64175590, [email protected]
1 Centri dello studio in 1 paesi
Shanghai Municipality
Fudan University Shanghai Cancer Center, Shanghai, Shanghai Municipality, 200032, China
wang hongxia, PHD, Contatto, 021-64175590, [email protected]
wang hongxia, PHD, Contatto
In arruolamento