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NCT Number: NCT07339839

Glecirasib Combined With Ivonescimab for First-line Treatment of KRAS G12C-mutated NSCLC

This study evaluates the safety, tolerability, maximum tolerated dose (MTD), dose-limiting toxicities (DLTs), and recommended phase II dose (RP2D) of Glecirasib in combination with Ivonescimab in patients with previously untreated, KRAS G12C-mutated, locally advanced or metastatic non-small cell lung cancer (NSCLC) with PD-L1 TPS ≥1%. The study includes a Phase I 3+3 dose-escalation stage followed by a Phase II Simon two-stage design to assess preliminary antitumor efficacy.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed written informed consent.
  • Age ≥18 years.
  • Newly diagnosed, unresectable, locally advanced (ineligible for curative concurrent - chemoradiotherapy) or metastatic NSCLC per AJCC 9th edition.
  • KRAS G12C mutation confirmed by validated testing.
  • PD-L1 TPS ≥1%.
  • ≥1 measurable lesion per RECIST v1.1.
  • No prior systemic therapy for advanced/metastatic NSCLC; prior adjuvant therapy allowed if completed >6 months before dosing and toxicities recovered to ≤Grade 1.
  • ECOG PS 0-2.
  • Life expectancy >3 months
  • Adequate organ function (hematologic, hepatic, renal, coagulation per protocol thresholds)
  • Negative pregnancy test for women of childbearing potential; adequate contraception for men and women through 3 months post-treatment
  • Willing and able to comply with study procedures and follow-up.

Exclusion criteria

  • History of other malignancies (exceptions: cured basal cell carcinoma, cervical carcinoma in situ)
  • Predominant squamous NSCLC, small cell carcinoma, or neuroendocrine carcinoma.
  • Other actionable drivers (EGFR, ALK, ROS1, RET, BRAF, NTRK, MET, etc.).
  • Known hypersensitivity to study drugs.
  • Prior PD-1/PD-L1 inhibitors or KRAS inhibitors.
  • Active autoimmune disease or autoimmune disease history requiring systemic therapy.
  • Systemic immunosuppressive therapy within 14 days prior to first dose.
  • Symptomatic ascites/pleural effusion needing recurrent drainage.
  • Significant cardiovascular disease (NYHA ≥2, MI within 1 year, uncontrolled arrhythmias).
  • Active infection, unexplained fever >38.5°C.
  • Interstitial lung disease or pneumonitis.
  • HIV infection or other immunodeficiency.
  • Live vaccines within 4 weeks.
  • Substance abuse, alcoholism, or psychiatric disorders impairing compliance.
  • Unable to swallow oral medication.
  • Any condition that may interfere with study participation or interpretation as judged by investigator.

Treatment and study plan

Glecirasib

Drug

For Phase I Dose Escalation, Glecirasib includes 2 dose cohorts: 600 mg QD and 800 mg QD, respectively, to determine the Glecirasib PR2D dose for the Phase II study.

Other names: JAB-21822

Ivonescimab

Drug

Administered intravenously at 20 mg/kg, every 3 weeks (Q3W).

Other names: AK112

Primary outcomes

  1. Phase I: Maximum Tolerated Dose (MTD)

    Time frame: 21 days after the first dose.

    The MTD is determined using a standard 3+3 dose-escalation design. It is defined as the dose level prior to the dose at which ≥2 out of 3-6 patients experience a Dose-Limiting Toxicity (DLT) within the first 21 days of treatment

  2. Phase I: Incidence of Dose-Limiting Toxicities (DLTs)

    Time frame: 21 days after the first dose.

    Evaluation of toxicities related to the study drugs, including hematologic and non-hematologic toxicities as defined in the protocol.

  3. Phase I: Recommended Phase 2 Dose (RP2D)

    Time frame: 21 days after the first dose.

    The RP2D of Glecirasib in combination with Ivonescimab will be selected based on the comprehensive evaluation of the MTD, DLT occurrences, and overall safety data observed during the Phase I escalation phase. This dose will then be utilized in the Phase II Simon's two-stage expansion to further evaluate efficacy and safety.

  4. Phase II: Objective Response Rate (ORR)

    Time frame: Assessed up to 24 months

    The proportion of patients who achieve a Complete Response (CR) or Partial Response (PR) based on RECIST v1.1.

Secondary outcomes

  1. Disease Control Rate (DCR)

    Time frame: Up to 24 months

    Proportion of patients with CR, PR, or SD.

  2. Progression-Free Survival (PFS)

    Time frame: Up to 24 months

    Time from the first dose to the first documented disease progression or death from any cause.

  3. Duration of Response (DOR)

    Time frame: Up to 24 months

    Time from the first documented response (CR or PR) to progression or death.

  4. Overall Survival (OS)

    Time frame: Up to 24 months

    Time from the first dose to death from any cause

  5. Incidence of Adverse Events (AEs)

    Time frame: From first dose enrollment through 28 days after the last dose.

    Severity of AEs graded by CTCAE v5.0

Study contacts

Contact information is provided by the study sponsor or research team.

Zhijie Wang, MD

CONTACT

[email protected]

010-67781331

Sponsors and collaborators

Lead sponsor

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Other

Registry information

Official study title

Glecirasib Combined With Ivonescimab for First-line Treatment of KRAS G12C-mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer: A Prospective, Multi-center, Phase I/II Clinical Study

Important dates

Study start
2026
Primary completion
2027
Study completion
2029
First posted
Jan 14, 2026
Registry last updated
Jan 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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