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Clinical Study of Ivonescimab Combined With Concurrent Chemoradiotherapy in the Treatment of Advanced Non-small Cell Lung Cancer

10 november 2026 bijgewerkt door: Guizhou Medical University

A Prospective Exploratory Phase II Clinical Study of Ivonescimab Combined With Concurrent Chemoradiotherapy in the Treatment of Patients With Advanced Non-Small Cell Lung Cancer

This prospective, exploratory study will evaluate the objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and toxicity of ivonescimab plus chemotherapy for 2-4 cycles after concurrent chemoradiotherapy, followed by 2 years of ivonescimab maintenance therapy, in patients with stage IV non-small cell lung cancer (NSCLC). The findings will be compared with those of previous studies and with our institutional data on patients with stage IV NSCLC who received concurrent chemoradiotherapy followed by PD-1 inhibitor plus chemotherapy for 2-4 cycles and then 2 years of PD-1 inhibitor maintenance therapy. This comparison may demonstrate that, after concurrent chemoradiotherapy for stage IV NSCLC, ivonescimab plus chemotherapy for 2-4 cycles followed by 2 years of ivonescimab maintenance therapy achieves superior efficacy compared with PD-1 inhibitor plus chemotherapy for 2-4 cycles followed by 2 years of PD-1 inhibitor maintenance therapy, with a comparable toxicity profile.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Geschat)

40

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

    • Guizhou
      • Guiyang, Guizhou, China, 550008
        • the Affiliated Cancer Hospital of Guizhou Medical University
        • Contact:
        • Contact:
        • Hoofdonderzoeker:
          • Dongdong Cao, MSc
        • Hoofdonderzoeker:
          • Wengang Yang, MSc
        • Hoofdonderzoeker:
          • Mei Liu, BSc
        • Hoofdonderzoeker:
          • Zu Ma, BSc
        • Hoofdonderzoeker:
          • Qingsong Li, MD

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 75 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Have fully understood this study and voluntarily signed the Informed Consent Form (ICF)

  • Aged 18 to 75 years, regardless of gender

  • Previously untreated, histopathologically or cytologically confirmed unresectable PD-L1 TPS ≥ 1% Stage IV non-small cell lung cancer

  • Have measurable lesions according to Response Evaluation Criteria in Solid Tumors version 1.1

  • Have adequate pulmonary function tests (PFTs)

  • Subjects must be able to provide a prior driver gene report based on tissue or blood testing, and the test results must show that targetable driver genes such as EGFR sensitive mutations, ALK rearrangement or fusion, and ROS1 fusion are all negative; or if a certain type of driver gene is positive but the targeted drug is not available, the subject may be enrolled. If the subject does not have a driver gene test report, tumor samples (archived or fresh, primary or metastatic) or blood samples must be collected before enrollment for driver gene testing to confirm negativity (at a local laboratory or central laboratory)

  • ECOG performance status score of 0-1

  • Adequate organ and bone marrow function

    ① Hematology: Absolute neutrophil count (ANC) ≥ 1500/μL; Platelets ≥ 100,000/μL; Hemoglobin ≥ 9.0 g/dL or ≥ 5.6 mmol/L.

    ② Renal: Serum creatinine ≤ 1.5 × ULN or calculated creatinine clearance (CrCl) ≥ 60 mL/min (using the Cockcroft-Gault formula).

    ③ Hepar: Total bilirubin ≤ 1.5 × ULN, or for subjects with total bilirubin levels > 1.5 × ULN, direct bilirubin within normal limits; AST (SGOT) and ALT (SGPT) ≤ 2.5 × ULN.

    ④ Adequate coagulation function: International Normalized Ratio (INR) and Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN; Known left ventricular ejection fraction (LVEF) ≥ 50%; Urine protein < 1+ or if urine protein is 1+, further 24-hour urine protein quantification < 1.0 g.

  • Endocrine System: Thyroid-stimulating hormone (TSH) within normal limits. Note: If TSH is not within the normal range at baseline, the subject may still meet the inclusion criteria if T3 and free T4 are within the normal range;Coagulation function: International Normalized Ratio (INR) or Prothrombin Time (PT), Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN, except for subjects receiving anticoagulant therapy, as long as PT or aPTT is within the intended therapeutic range of the anticoagulant drug.

  • Willing and able to comply with the study plan's visits, treatment plans, laboratory tests, and other study procedures.

  • Childbearing age women must have a serum pregnancy test within 3 days before the first dose, and the result must be negative. Female subjects of childbearing age and male subjects with partners of childbearing age must agree to use highly effective methods of contraception during the study and for 180 days after the last dose of the study drug.

Exclusion Criteria:

  • Presence of resectable or metastatic disease
  • History of interstitial lung disease, drug-induced interstitial lung disease, or radiation pneumonitis requiring steroid therapy, or currently receiving drug treatment or other clinical interventions, or presence of active pulmonary interstitial lesions or imaging findings of interstitial lung disease.
  • Known history of active tuberculosis
  • Known active infection requiring systemic therapy
  • Any known or suspected autoimmune disease or immunodeficiency, except for: patients with a history of hypothyroidism who do not require hormone therapy or are receiving physiological doses of hormone replacement therapy; patients with stable blood glucose-controlled type 1 diabetes.
  • Uncontrolled active hepatitis B (defined as positive hepatitis B surface antigen [HBsAg] test at screening with HBV-DNA levels above the upper limit of normal of the study center's laboratory; patients with HBV-DNA <500 IU/mL within 28 days before enrollment who have received at least 14 days of standard local antiviral therapy and are willing to continue antiviral therapy during the study may be enrolled); active hepatitis C (defined as positive hepatitis C virus surface antibody [HCsAb] test at screening with positive HCV-RNA).
  • Known human immunodeficiency virus (HIV) infection (known HIV antibody positive)
  • Vaccination with live vaccines within 30 days before the first dose, including but not limited to: mumps, rubella, measles, varicella/zoster (chickenpox), yellow fever, rabies, BCG, and typhoid vaccine (inactivated virus vaccines are allowed).
  • History of severe allergic reactions to other monoclonal antibodies;
  • Known severe or uncontrolled underlying diseases
  • Patients with a history of another malignancy within 5 years before the first dose, other than non-small cell lung cancer, are excluded. This exclusion does not apply to malignancies with a negligible risk of metastasis or death (e.g., expected disease-free survival >5 years) that are expected to achieve a curative outcome after treatment (e.g., adequately treated cervical carcinoma in situ, basal cell or squamous cell skin cancer, or ductal carcinoma in situ treated with curative-intent surgery).
  • Class III-IV congestive heart failure (New York Heart Association classification), poorly controlled and clinically significant arrhythmias.
  • Any arterial thrombosis, embolism, or ischemia within 6 months before enrollment, such as myocardial infarction, unstable angina, cerebrovascular accident, or transient ischemic attack.
  • Female subjects who are pregnant, breastfeeding, or planning to become pregnant during the study.
  • Investigators consider other conditions that may make the patient unsuitable for participation in this clinical trial.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: ivonescimab combined with chemotherapy for 2-4 cycles followed by ivonescimab maintenance therapy

After concurrent chemoradiotherapy, patients received 2-4 cycles of ivonescimab combined with chemotherapy, with each 3-week period defined as one dosing cycle. On Day 1 of each treatment cycle, ivonescimab was administered first by intravenous infusion; after an interval of at least 30 minutes, pemetrexed or paclitaxel/albumin-bound paclitaxel was administered intravenously. On Day 2, carboplatin or cisplatin was administered intravenously. Patients without disease progression received ivonescimab maintenance therapy for up to 2 years or until discontinuation due to toxicity-related intolerance.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Objective response rate
Tijdsspanne: From the first dose to week 24 (±7 days)

Confirmed ORR assessed by investigators per RECIST 1.1, i.e., the proportion of subjects with CR+PR

From the first dose to week 24 (±7 days)
Median progression-free survival
Tijdsspanne: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Weiwei Ouyang, the affiliated cancer hospital of guizhou medical university

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

30 oktober 2026

Primaire voltooiing (Geschat)

30 oktober 2028

Studie voltooiing (Geschat)

30 oktober 2029

Studieregistratiedata

Eerst ingediend

26 oktober 2026

Eerst ingediend dat voldeed aan de QC-criteria

10 november 2026

Eerst geplaatst (Werkelijk)

13 november 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

13 november 2026

Laatste update ingediend die voldeed aan QC-criteria

10 november 2026

Laatst geverifieerd

1 november 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

JA

Beschrijving IPD-plan

We will share the de-identified IPD that underlie the results reported in the publication, including baseline variables, randomization assignment, primary and secondary outcomes, and adverse events, together with a data dictionary. Data not required to reproduce the published results, such as [imaging data/genomic data/free-text fields], will not be shared.

IPD delen Ondersteunend informatietype

  • LEERPROTOCOOL
  • SAP
  • MVO

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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