GSK3359609 Plus Tremelimumab for the Treatment of Advanced Solid Tumors

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

November 26, 2018

Primary Completion Date

June 25, 2021

Study Completion Date

September 16, 2021

Conditions
Neoplasms
Interventions
DRUG

feladilimab

feladilimab is humanized anti-ICOS agonist immunoglobulin G (IgG) 4 monoclonal antibody (mAb), which will be administered as an intravenous (IV) infusion once every 3 weeks.

DRUG

Tremelimumab

Tremelimumab is humanized anti-CTLA-4 IgG2 mAb, which will be administered as an IV infusion once every 3 weeks for 6 doses, thereafter once every 12 weeks .

DRUG

Docetaxel

Docetaxel is a microtubule stabilizer which will be administered as an IV infusion once every 3 weeks at a dose of 75 milligrams per meter square (mg/m\^2).

DRUG

Paclitaxel

Paclitaxel is a microtubule stabilizer which will be administered as an IV infusion once weekly at a dose of 80 mg/m\^2.

DRUG

Cetuximab

Cetuximab is a recombinant, human/mouse chimeric anti-estimated glomerular filtration rate (EGFR) mAb. Cetuximab will be administered at a loading dose of 400 mg/m\^2 followed by 250 mg/m\^2 once weekly.

Trial Locations (8)

3000

GSK Investigational Site, Melbourne

10032

GSK Investigational Site, New York

15232

GSK Investigational Site, Pittsburgh

78229

GSK Investigational Site, San Antonio

02215

GSK Investigational Site, Boston

10016-4744

GSK Investigational Site, New York

K1H 8L6

GSK Investigational Site, Ottawa

M5G 2M9

GSK Investigational Site, Toronto

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

MedImmune LLC

INDUSTRY

lead

GlaxoSmithKline

INDUSTRY