Trial Review

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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT05993455




Registration number
NCT05993455
Ethics application status
Date submitted
3/08/2023
Date registered
15/08/2023
Date last updated
15/08/2023

Titles & IDs
Public title
A Phase 2 Basket Trial in Which Patients With Advanced Solid Tumors Carrying the KRAS G12C mUtation Receive Treatment With a Combination of Sotorasib and Panitumumab
Scientific title
A Phase 2 Basket Trial in Which Patients With Advanced Solid Tumors Carrying the KRAS G12C mUtation Receive Treatment With a Combination of Sotorasib and Panitumumab (KRAUS)
Secondary ID [1] 0 0
KRAUS
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Efficacy 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Experimental: Oral sotorasib + IV Panitumumab - Oral sotorasib at a dose of 960 mg once daily with Panitumumab is administered intravenously (IV) at a dose of 6 mg/kg every 14 days, infused over 60 minutes (= 1,000 mg) or 90 minutes (\> 1,000 mg).
Comparator / control treatment
Control group

Outcomes

Eligibility
Key inclusion criteria
* Patients who have consented to participate in the KOSMOS-II observational master study.
* Age of 19 years or older.
* Histologically confirmed locally advanced or metastatic solid tumors (excluding non-small cell lung cancer and colorectal cancer) with KRAS G12C mutation detected through local next-generation sequencing analysis.
* Local advanced or metastatic disease with disease progression or unavailability of standard treatment options for the first-line anti-cancer therapy.
* Measurable lesions according to RECIST v1.1 (lesions that have not experienced disease progression after radiation therapy are excluded).
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
* Adequate bone marrow and organ function as described below:

? Bone Marrow: - Absolute neutrophil count (ANC) = 1,500/mm3 - Platelet count (PLT) = 100,000/mm3 - Hemoglobin (Hb) = 9 g/dL

? Liver Function:
* Total bilirubin = 1.5 X upper limit of normal (ULN). If liver metastasis is present, total bilirubin up to = 3 X ULN is allowed. For patients with Gilbert's syndrome, total bilirubin up to = 3 X ULN and direct bilirubin within the normal range is allowed.
* Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 3 X ULN (or = 5 X ULN if liver metastasis is present).

? Renal Function: - Creatinine clearance = 30 mL/min/1.73m2 (using the Cockcroft-Gault formula).
* Estimated life expectancy of at least 3 months according to the investigator's judgment.
* Ability to take oral medications.
* Understanding and compliance with the clinical trial protocol and ability to provide informed consent by signing the informed consent form.
Minimum age
19 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Patients who have not received previous sotorasib treatment or monoclonal antibodies against epidermal growth factor receptor (EGFR) such as cetuximab or panitumumab.
* Absence of active brain metastasis or leptomeningeal metastasis (Patients with previously treated brain metastasis or leptomeningeal metastasis with radiation therapy and/or surgery [including radiosurgery] and are neurologically stable can be eligible for enrollment).
* No significant cardiovascular events within the past 6 months, such as:

.NYHA Class 3 or higher congestive heart failure. .Unstable angina or myocardial infarction. .Uncontrolled or symptomatic atrial fibrillation. .QTc prolongation (> 480 milliseconds).

* No history of stroke within the past 6 months (including transient ischemic attack).
* No diagnosis of another malignancy within 2 years prior to enrollment (excluding superficial basal cell carcinoma or squamous cell carcinoma, cervical intraepithelial neoplasia, prostate cancer under active surveillance, and well-differentiated thyroid cancer that has undergone definitive surgery).
* Pregnant or breastfeeding women.
* Participants who do not agree to effective contraception* during the clinical trial.
* Sexually active female participants of childbearing potential and their partners must agree to use medically acceptable contraception (e.g., male condoms, female condoms, or the combined use of barrier methods and spermicidal gel) during the clinical trial period and for up to 6 months after the last administration of the investigational drug.
* Male participants who have not undergone vasectomy must agree to use barrier contraception (condoms) and are prohibited from providing sperm donations until 6 months after the last administration of the investigational drug.
* Participants with active hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) infection, except under the following conditions:
* Participants who are positive for HBsAg (Hepatitis B surface antigen) can be enrolled if ALT is within the normal range and HBV DNA is <2,000 IU/ml while receiving antiviral prophylaxis for hepatitis B reactivation.
* Participants who are negative for HBsAg but positive for Hepatitis B core antibody (IgG anti-HBc) can be enrolled if HBV DNA is quantifiable but below the limit of quantification.
* Participants who are positive for anti-HCV Ab can be enrolled if HCV RNA is quantifiable but below the limit of quantification.
* Participants with planned major surgery during the clinical trial.
* Other clinically significant disorders deemed unsuitable for the clinical trial by the investigator.

Study design
Purpose of the study
Treatment
Allocation to intervention
NA
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 2
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
3/07/2023
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
31/12/2023
Actual
Sample size
Target
24
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Primary sponsor type
Other
Name
Korea University Anam Hospital
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT05993455