This is a Phase 1 open label study to evaluate the tolerability, safety, immunogenicity, and efficacy of SW1115C3, a neoantigen mRNA personalised cancer vaccine, in patients with advanced malignant solid tumours.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Subcutaneous Injection
Pindara Private Hospital
Benowa, Queensland, Australia
RECRUITINGPeninsula & South Eastern Haematology and Oncology Group
Frankston, Victoria, Australia
RECRUITINGOne Clinical Research
Nedlands, Western Australia, Austria
RECRUITING,Dose-limiting toxicity incidence (participants who experience DLT)
Time frame: 21 day
Objective response rate(ORR) assessment per RECIST Version 1.1
Time frame: 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.