COVID-19 Prevention and Treatment in Cancer; a Sequential Multiple Assignment Randomised Trial; C-SMART study.Arm 3: Effect of selinexor in cancer patients with moderate COVID-19 infection.

Peter MacCallum Cancer Centre0 sites3 target enrollmentAugust 26, 2020

Overview

No summary available.

Registry

who.int

Start Date

August 26, 2020

End Date

March 30, 2022

Last Updated

2 years ago

Study Type

Interventional

Sex

All

Sponsor

Peter MacCallum Cancer Centre

•1\. Age equal to or greater than 18 years of age.
•2\. Any haematological or solid tumour
•3\. Current or within the last 12 months received cancer related treatment such as chemotherapy, radiotherapy or targeted small molecule, cellular therapy or immune\-modulating therapy
•4\. Signed written and verbal informed consent
•5\. Laboratory confirmation of SARS\-CoV\-2 by PCR as per local laboratory assays
•6\. Hospitalised
•7\. Symptoms of COVID\-19 such as:
•a. Fever equal to or greater than 38 degrees Celsius OR
•b. Tachypnoea respiratory rate equal to or greater than 20 breaths/min OR
•c. Pulse Oxygen saturation (SpO2\) equal to or less than 94%

•1\. Unable to take oral medication
•2\. Any known allergic reactions to selinexor or concomitant medication\-related contra\-indications to selinexor.
•3\. Severe critical COVID\-19 infection defined as:
•a) Requiring invasive or non\-invasive mechanical ventilation, ECMO
•b) Anticipated unlikely to survive within 48 hours
•4\. In the opinion of the investigator and primary oncologist, participation in the study would not be in the best interests of the participant
•5\. Severe renal impairment defined as creatinine clearance (CrCL) \< 20ml/min as calculated using the Cockcroft Gault formula
•6\. Severe hepatic impairment defined as aspartate transaminase (AST) or alanine transaminase (ALT) \> 5 x upper limit of normal (ULN)