A Study of JAB-21822 in Patients With KRAS p.G12C Mutated Pancreatic Cancer

Sponsor
Jacobio Pharmaceuticals Co., Ltd. (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT06008288
Collaborator
(none)
69
2
1
24
34.5
1.4

Study Details

Study Description

Brief Summary

This study is to evaluate the efficacy and safety of JAB-21822 monotherapy in adult participants with KRAS G12C mutated pancreatic cancer

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

This is a single-arm, open-label, multicenter phase 2 study to evaluate the efficacy and safety of JAB-21822 monotherapy in adult participants with advanced KRAS p.G12C mutated pancreatic cancer.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
69 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Phase 2, Multi-Center, Open-Label, Single-arm Study to Evaluate the Efficacy and Safety of JAB-21822 Monotherapy in Patients With Locally Advanced or Metastatic KRAS p.G12C Mutated Pancreatic Cancer
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
May 1, 2025
Anticipated Study Completion Date :
Nov 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: JAB-21822

Monotherapy

Drug: JAB-21822
800mg, orally QD with 21 days each cycle, treatment till disease progression or intolerable toxicity or withdraw for other reasons
Other Names:
  • Glecirasib
  • Outcome Measures

    Primary Outcome Measures

    1. Objective response rate (ORR) by independent central radiological review (IRC) according to RECIST 1.1. [Approximately 1.5 years]

      ORR is defined as the proportion of participants with confirmed complete response or partial response by IRC according to RECIST 1.1.

    Secondary Outcome Measures

    1. Duration of response (DOR) [Approximately 1.5 years]

      DOR is defined as the time from date of the first objective tumor response (CR or PR) to the first documentation of either Progression of Disease (PD) or death due to any cause, whichever occurs first.

    2. Time to response (TTR) by IRC according to RECIST 1.1 [Approximately 1.5 years]

      TTR is defined as the duration of time between the date of the first dose and the date of first documented response of either CR or PR.

    3. Progression-free survival (PFS) by IRC according to RECIST 1.1 [Approximately 1.5 years]

      PFS is defined as time from the first dose until disease progression or death from any cause, whichever occurs first.

    4. Disease control rate (DCR) by IRC according to RECIST 1.1 [Approximately 1.5 years]

      DCR is defined as the proportion of participants with BOR of CR or PR or stable disease (SD)

    5. CA19-9 response rate [Approximately 1.5 years]

      CA19-9 response rate is defined as the proportion of participants with CA19-9 response (achieving ≥50% decrease in CA19-9 serum levels).

    6. Overall survival (OS) [Approximately 2.0 years]

      OS is defined as time from date of the first dose to date of death due to any cause.

    7. Number of participants with adverse events [Approximately 1.5 years]

      Participants will be assessed for incidence and severity of AEs according to NCI-CTCAE 5.0 criteria

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Histopathologically or cytologically confirmed pancreatic cancer with KRAS p.G12C mutation identified through molecular testing.

    • Previously progressed on or after gemcitabine-based and/or FOFIRINOX/mFOFIRINOX chemotherapy, no more than 3 lines of prior systemic therapies. Participants with disease recurrence during or within 6 months after adjuvant therapy can be included.

    • Participants with MSI-H/dMMR must experience anti-PD-1 therapy.

    Exclusion Criteria:
    • Previously received a KRAS G12C inhibitor.

    • History of interstitial lung disease, non-infectious pneumonia, or uncontrolled lung disease (including pulmonary fibrosis, acute lung disease, etc.).

    • Uncontrolled pleural effusion, pericardial effusion, or ascites.

    • Mean QT interval corrected for heart rate using Fridericia's formula (QTcF) ≥470 ms calculated from 3 electrocardiograms.

    • Use of a drug with known risk of torsades de points (TdP) within 14 days prior to the first dose.

    • Cannot discontinue a proton pump inhibitor (PPI) or H2 receptor blocker within 3 days or 5 half-lives (whichever is longer) prior to the first dose.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beijing Cancer Hospital Beijing Beijing China 100142
    2 Peking Union Medical College Hospital Beijing Beijing China 100730

    Sponsors and Collaborators

    • Jacobio Pharmaceuticals Co., Ltd.

    Investigators

    • Study Director: Jacobio Pharmaceuticals, Jacobio Pharmaceuticals

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Jacobio Pharmaceuticals Co., Ltd.
    ClinicalTrials.gov Identifier:
    NCT06008288
    Other Study ID Numbers:
    • JAB-21822-2001
    First Posted:
    Aug 23, 2023
    Last Update Posted:
    Aug 23, 2023
    Last Verified:
    Aug 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 23, 2023