- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07874282
Phase II Study to Evaluate Telisotuzumab Adizutecan in Combination With RC148(ABBV-1480) as First-Line Treatment for Patients With Non-Squamous Non-Small-Cell Lung Cancer
3. November 2026 aktualisiert von: RemeGen Co., Ltd.
Phase II Clinical Study to Evaluate the Efficacy and Safety of Telisotuzumab Adizutecan in Combination With RC148 as First-Line Therapy for Non-Squamous Non-Small-Cell Lung Cancer
To Evaluate the Safety, Tolerability, and Preliminary Antitumor Efficacy of RC148 in Combination with Telisotuzumab adizutecan as First-line Treatment for Locally Advanced or Metastatic Non-Squamous Non-Small-Cell Lung Cancer
Studienübersicht
Status
Noch keine Rekrutierung
Studientyp
Interventionell
Einschreibung (Geschätzt)
200
Phase
- Phase 2
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Jiang Guo
- Telefonnummer: 010-65384976
- E-Mail: jiang.guo@remegen.com
Studienorte
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, China
- Shanghai East Hospital, Tongji University School of Medicine
-
-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre bis 80 Jahre (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria:
- Voluntarily agrees to participate in the study and provides signed informed consent
- Willing and able to comply with study and follow-up procedures
- Male or female, aged 18-80 years
- Expected survival≥3 months
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Histopathologically or cytologically confirmed locally advanced or metastatic non-squamous NSCLC not amenable to curative-intent therapy
- No prior systemic anti-neoplastic therapy for advanced or metastatic non-squamous NSCLC
- At least one measurable non-cerebral lesion per RECIST v1.1
- Availability of c-Met expression, PD-L1 expression and driver gene test results including at minimum EGFR and ALK for enrollment
- Adequate cardiac, bone-marrow, hepatic, renal and coagulation function meeting relevant criteria
- Female study participants must be post-menopausal, surgically sterilized, or, if of child-bearing potential, have a negative serum pregnancy test within 7 days prior to the first dose, agree to use at least one medically-accepted contraceptive method during study treatment and for 12 months after the end of study treatment, and refrain from oocyte donation and breastfeeding during this period; male study participants must agree to use at least one medically-accepted contraceptive method during study treatment and for 12 months after the end of study treatment and refrain from sperm donation during this period
Exclusion Criteria:
- Histologically confirmed presence of any squamous NSCLC, small-cell carcinoma, neuroendocrine carcinoma, or sarcoma component
- Known positive driver gene or gene mutations with approved first-line treatment options
- Presence of active brain metastases
- Screening-period imaging shows obvious tumor necrosis or cavitation, with bleeding risk upon study entry as judged by the investigator
- Received thoracic radiotherapy >30 Gy within 6 months prior to randomization; palliative local therapy for non-target lesions within 2 weeks prior to randomization; non-specific immunomodulatory therapy within 2 weeks prior to the first dose of study drug; or traditional Chinese herbal/proprietary medicine with anti-neoplastic indications within 1 week prior to randomization
- Prior immunotherapy, including immune checkpoint inhibitors, immune checkpoint agonists, immune-cell therapy, or any other therapies targeting tumor immune mechanisms
- Prior systemic anti-neoplastic therapies other than chemotherapy and PD-1/PD-L1 antibodies
- Systemic treatment with corticosteroids or other immunosuppressive medications within 2 weeks prior to randomization
- Administration of any live or live-attenuated vaccine within 4 weeks prior to randomization, or planned administration of any live or live-attenuated vaccine during the study
- Participation in another clinical trial within 4 weeks prior to randomization
- Major surgery, interventional therapy, or severe trauma within 4 weeks prior to randomization, or planned major surgery during the study period; core-needle biopsy or other minor surgery within 7 days prior to the first dose
- History of severe coagulation disorders; or subjects receiving anticoagulant therapy, excluding prophylactic-dose anticoagulants such as low-molecular-weight heparin
- Toxicities from prior anti-neoplastic therapy not recovered to Grade 0-1 as defined by CTCAE v6.0; except for alopecia, pigmentation, expected irrecoverable endocrinopathies from prior immunotherapy that are stably controlled with medication, and other conditions assessed by the investigator not interfering with study drug treatment
- For subjects previously exposed to PD-1/PD-L1 inhibitors: prior occurrence of immune-related adverse events (irAEs) Grade 3 or higher due to immunotherapy, irAEs leading to permanent treatment discontinuation, Grade 2 immune-related cardiac toxicity, or any-grade neurological or ocular irAEs; prior adverse events requiring immunosuppressive agents other than corticosteroids, or recurrent adverse events during prior immunotherapy requiring re-initiation of systemic corticosteroid therapy
- Presence of severe acute or chronic infection
- Hemoptysis, active gastrointestinal bleeding, peptic ulcer, epistaxis, or other bleeding events requiring intervention within 4 weeks prior to randomization; or severe esophagogastric varices, vasculitis, vascular ulcer, aneurysm, or vascular dissection judged by the investigator to carry a high bleeding risk
- Severe arterial/venous thromboembolic events or cerebrovascular accident within 6 months prior to the first dose
- Active or clinically significant cardiac disease
- History of interstitial lung disease or pulmonary inflammation requiring systemic steroid therapy; or chest-CT at screening showing any evidence of active ILD/pulmonary inflammation, idiopathic pulmonary fibrosis, organizing pneumonia, treatment-induced pneumonitis, idiopathic pneumonia, radiation pneumonitis, severe impaired pulmonary function, or acute exacerbation of chronic obstructive pulmonary disease within 1 month prior to randomization
- History of gastrointestinal perforation and/or fistula, or gastrointestinal obstruction within 6 months prior to randomization
- Presence of systemic diseases that are not stably controlled as judged by the investigator
- Active autoimmune disease, or prior history of autoimmune disease with potential for recurrence
- Subjects with a history of other acquired or congenital immunodeficiency diseases, or history of organ transplantation
- Known hypersensitivity or delayed-type allergic reaction to any components of the study drug or analogous medicinal products
- Clinically symptomatic third-space effusion or third-space effusion requiring intervention
- Other malignancy diagnosed within 3 years prior to initiation of study drug administration
- Poor compliance; subjects expected to be unable to cooperate with completion of trial procedures
- Any other past or present disease, abnormal physical finding, or laboratory abnormality, in the investigator's opinion, rendering the subject unsuitable for study drug administration, likely to confound interpretation of study results, or placing the subject at high-risk
- Local or systemic disease not caused by malignancy, or diseases/symptoms secondary to the tumor, that may result in substantial medical risk and/or uncertainty in survival-time assessment, such as manifestations of cachexia
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Dose1:Telisotuzumab adizutecan plus RC148(ABBV-1480)
|
Dose1 Dose2 |
|
Experimental: Dose2:Telisotuzumab adizutecan plus RC148(ABBV-1480)
|
Dose1 Dose2 |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Objective Response Rate assessed by the investigators according to RECIST v1.1
Zeitfenster: 24 months
|
24 months
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
1. November 2026
Primärer Abschluss (Geschätzt)
1. Dezember 2027
Studienabschluss (Geschätzt)
1. Februar 2029
Studienanmeldedaten
Zuerst eingereicht
30. September 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
9. Oktober 2026
Zuerst gepostet (Tatsächlich)
14. Oktober 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
6. November 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
3. November 2026
Zuletzt verifiziert
1. November 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- RC148-A201
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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