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Evaluating Ivonescimab in PD-1 Resistant Recurrent or Metastatic Nasopharyngeal Carcinoma (AK112)

27 april 2026 bijgewerkt door: National University Hospital, Singapore

Phase II Open-label Study Evaluating Ivonescimab in PD-1 Resistant Recurrent or Metastatic Nasopharyngeal Carcinoma

This study is designed as a single-arm, open-label, phase II trial to evaluate the efficacy and safety of ivonescimab in patients with recurrent or metastatic nasopharyngeal carcinoma (NPC) who have progressed on prior an immune checkpoint inhibitor and platinum-based chemotherapy.

Studie Overzicht

Toestand

Nog niet aan het werven

Interventie / Behandeling

Gedetailleerde beschrijving

Participants will receive intravenous ivonescimab at a dose of 20 mg/kg administered every 3 weeks until disease progression, intolerable toxicities, or withdrawal from the study. All study treatments will be administered in an outpatient setting.

Participants will undergo clinical assessments every 3 weeks during the treatment period. Imaging assessments will be conducted every 6 weeks (±7 days) for the first 24 weeks of treatment, followed by every 9 weeks (±7 days) thereafter, continuing until treatment discontinuation.

Studietype

Ingrijpend

Inschrijving (Geschat)

42

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

      • Singapore, Singapore
        • National University Cancer Institute, Singapore, National University Health System
        • Contact:

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

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Participant is eligible to be included in the study only if all the following criteria are met:

    1. The participant (or legally acceptable representative if applicable) provides written consent for the trial.
    2. Participant is at least 21 years of age on the day of signing informed consent
    3. Has a locally or centrally determined histologically or cytologically confirmed diagnosis of Epstein Barr Virus (EBV)-positive nasopharyngeal carcinoma Note: The EBV status is to be determined by the EBV-encoded small RNA in situ hybridization (EBER in situ hybridization [ISH]) assay. If EBV-positive status has been previously determined by EBER ISH assay, then no re-testing is required. If EBV status by EBER ISH assay has not been previously determined, tumour tissue from archival tissue may be submitted for EBV determination.
    4. Has recurrent or metastatic (R/M) disease not amenable to curative local therapy (surgery or radiation)
    5. Must have seen at least 1 prior line of systemic treatment and has progressed on prior platinum-based chemotherapy and anti-PD1 therapy in the R/M setting OR Progressed within 6 months of previous multimodal therapy containing platinum-based chemotherapy and anti-PD1 therapy in the locally advanced setting.
    6. Has measurable disease based on iRECIST.
    7. Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
    8. Has an adequate organ function as defined in the following table (table 1). Specimens must be collected within 10 days prior to the start of study treatment
    9. Willing to provide blood and tumour tissue samples (newly obtained biopsy if clinically feasible or archival specimen) to support exploratory biomarker analysis.

Exclusion Criteria:

  • Participant is excluded from the study if ANY of the following criteria apply:

    1. Is currently participating in or has participated in a study of an investigational agent or has used an investigational device within 4 weeks prior to first dose of study treatment.
    2. Has prior anti-angiogenic therapy in the R/M setting or within 6 months as part of multimodality therapy in the locally advanced setting. [Applies to cohort A only]
    3. Has tumour that encases major arteries which in the opinion of the investigator carries high risk of vessel wall dehiscence.
    4. Has a condition requiring systemic steroid therapy (> 10 mg daily prednisone equivalents) or any other form of immunosuppressive therapy within 14 days prior to the first dose of trial treatment.

      Note: Inhaled or topical steroids and adrenal replacement doses <10 mg daily prednisone equivalents are permitted in the absence of active autoimmune disease. Patients are permitted to use topical, ocular, intra-articular, intranasal, and inhalational corticosteroids (with minimal systemic absorption). Physiologic replacement doses of systemic corticosteroids are permitted if < or = 10 mg/day prednisone equivalents. A brief course of corticosteroids for prophylaxis (e.g., contrast dye allergy) or for treatment of non-autoimmune conditions (e.g., delayed-type hypersensitivity reaction caused by contact allergen) is permitted.

    5. Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs).

      Note: Replacement therapy (e.g. thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc) is not considered a form of systemic treatment.

    6. Has a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis.
    7. Has hypersensitivity to ivonescimab or any of its components.
    8. Has a known additional malignancy that is progressing or has required active treatment within the past 3 years.

      Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, transitional cell carcinoma of urothelial cancer, or carcinoma in situ (e.g. breast or cervical carcinoma in situ) that have undergone potentially curative therapy are not excluded.

    9. Has an active infection requiring systemic therapy, or serious non-healing wound, ulcer or bone fracture.
    10. Uncontrolled hypertension (failure of diastolic blood pressure to fall below 90 mmHg, despite the use of ≥ 3 anti-hypertensive drugs or systolic blood pressure greater than 150 mmHg).
    11. Recent cardiovascular thromboembolic event, such as the following:

      1. Cardiac chest pain, defined as moderate pain that limits instrumental activities of daily living, ≤ 4 weeks before enrolment
      2. Symptomatic pulmonary embolism ≤ 4 weeks before enrolment
      3. Any history of acute myocardial infarction ≤ 6 months before enrolment
      4. Any history of heart failure meeting New York Heart Association (NYHA) Classification III or IV (Appendix 4) ≤ 6 months before enrolment
      5. Any event of ventricular arrhythmia ≥ Grade 2 in severity ≤ 6 months before enrolment
      6. Any history of cerebrovascular accident ≤ 6 months before enrolment
    12. Persistent proteinuria of NCI-CTCAE Grade 3 or higher (> 3.5 g/24 hours, measured by urine protein/creatinine ratio on a random urine sample).
    13. Clinically significant bleeding (NCI-CTCAE Grade 3 or higher) within 30 days prior to start of study medication.
    14. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
    15. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
    16. Is pregnant, breastfeeding or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 120 days after the last dose of trial treatment.
    17. A woman of childbearing potential (WOCBP) who has a positive urine pregnancy test within 72 hours prior to randomization/allocation (see Appendix 3). If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.

      Note: If 72 hours have elapsed between the screening pregnancy test and the first dose of study treatment, another pregnancy test (urine or serum) must be performed and must be negative for subject to start receiving study medication.

    18. Has a known history of Human Immunodeficiency Virus (HIV). Note: No HIV testing is required unless mandated by local health authority.
    19. Known active Hepatitis B (defined as hepatitis B viral load detected) or Hepatitis C virus (defined as HCV RNA [qualitative] detected) infection. Patients on anti-virals but with undetectable Hepatitis B or C viral loads are not excluded.

      Note: No testing for Hepatitis B and Hepatitis C is required unless mandated by local health authority.

    20. History of having received a live virus vaccination (e.g., yellow fever, MMR, nasal flu, chicken pox or Zostavax) within 4 weeks prior to the first dose of trial treatment. Note: Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist®) are live attenuated vaccines and are not allowed.

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: Cohort A & B
We plan to enrol 32 patients with R/M NPC and who had failed prior platinum-based chemotherapy and anti-PD1 therapy in this study from (Cohort A) and we will have an additional cohort B consisting of 10 patients with R/M NPC and who had failed prior platinum-based chemotherapy, PD1-inhibitor and anti-angiogenic therapy.
Subjects will receive intravenous ivonescimab at a dose of 20 mg/kg administered every 3 weeks until disease progression, intolerable toxicities, or withdrawal from the study.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Objective Response Rate (ORR)
Tijdsspanne: Best response at 1 year
Objective Response Rate (ORR), defined as the proportion of patients with a confirmed complete response (CR) or partial response (PR) as assessed by investigator review using iRECIST
Best response at 1 year

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Progression-Free Survival (PFS)
Tijdsspanne: 3 years
defined as time from first dose of ivonescimab to documented disease progression or death from any cause, whichever occurs first, as assessed by iRECIST.
3 years
Overall Survival (OS)
Tijdsspanne: 3 years
defined as time from first dose of ivonescimab to death from any cause.
3 years
Duration of Response (DoR)
Tijdsspanne: 3 years
defined as time from the first documentation of objective response (Complete response or Partial response) to disease progression or death.
3 years
Disease Control Rate (DCR)
Tijdsspanne: 3 years
defined as the proportion of patients achieving Complete Response (CR) + Partial Response (PR) + Stable disease for at least 12 weeks.
3 years
Incidence, nature, and severity of adverse events (AEs) and serious adverse events (SAEs)
Tijdsspanne: from enrolment till 3 months after end of treatment
Incidence, nature, and severity of adverse events (AEs) and serious adverse events (SAEs) graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0.
from enrolment till 3 months after end of treatment
Frequency and proportion of treatment-related adverse events (TRAEs)
Tijdsspanne: from enrolment till 3 months after end of treatment
Treatment-related adverse events (TRAEs) graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0.
from enrolment till 3 months after end of treatment
Incidence of immune-related adverse events (irAEs)
Tijdsspanne: from enrolment till 3 months after end of treatment
Events will be identified based on clinical assessment and investigator attribution, summarized by type, frequency, and proportion of affected participants, and graded for severity according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE), version 5.0.
from enrolment till 3 months after end of treatment
Rates of dose delays, modifications, or treatment discontinuations due to adverse events.
Tijdsspanne: from enrolment till 3 months after end of treatment
Measures how many participants had their treatment delayed, adjusted, or stopped completely because of treatment side effects.
from enrolment till 3 months after end of treatment

Medewerkers en onderzoekers

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

Onderzoekers

  • Hoofdonderzoeker: Wan Qin Chong, National University Hospital, Singapore

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

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)

1 mei 2026

Primaire voltooiing (Geschat)

1 mei 2031

Studie voltooiing (Geschat)

1 mei 2031

Studieregistratiedata

Eerst ingediend

9 maart 2026

Eerst ingediend dat voldeed aan de QC-criteria

27 april 2026

Eerst geplaatst (Werkelijk)

4 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

4 mei 2026

Laatste update ingediend die voldeed aan QC-criteria

27 april 2026

Laatst geverifieerd

1 februari 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

Individual patient data will be available, including data dictionaries and all clinical data collected in the conduct of the trial, in a deidentified format. These will be available beginning 3 months after Article publication with no end date. other researchers should submit requests for access to the patient-level data to the corresponding author, including a proposal outlining their reasons for required data.

Following a signed data access agreement, the data will be made available by a link sent from the corresponding author to the requester.

IPD-tijdsbestek voor delen

They will be available beginning 3 months after Article publication with no end date.

IPD-toegangscriteria voor delen

other researchers should submit requests for access to the patient-level data to the corresponding author, including a proposal outlining their reasons for required data. Following a signed data access agreement, the data will be made available by a link sent from the corresponding author to the requester.

IPD delen Ondersteunend informatietype

  • LEERPROTOCOOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • 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

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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