Glecirasib
DrugFor 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
NCT Number: NCT07339839
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.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 1 / Phase 2
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
Administered intravenously at 20 mg/kg, every 3 weeks (Q3W).
Other names: AK112
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
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.
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.
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.
Time frame: Up to 24 months
Proportion of patients with CR, PR, or SD.
Time frame: Up to 24 months
Time from the first dose to the first documented disease progression or death from any cause.
Time frame: Up to 24 months
Time from the first documented response (CR or PR) to progression or death.
Time frame: Up to 24 months
Time from the first dose to death from any cause
Time frame: From first dose enrollment through 28 days after the last dose.
Severity of AEs graded by CTCAE v5.0
Contact information is provided by the study sponsor or research team.
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Other
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
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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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