Safety and Efficacy Study of PDR001 in Patients With Recurrent or Metastatic Nasopharyngeal Carcinoma

PHASE2CompletedINTERVENTIONAL
Enrollment

122

Participants

Timeline

Start Date

April 20, 2016

Primary Completion Date

November 5, 2019

Study Completion Date

February 19, 2021

Conditions
Nasopharyngeal Carcinoma
Interventions
DRUG

Spartalizumab

Spartalizumab was administered via intravenous infusion at a dose of 400 mg every 4 weeks (Q4W). Spartalizumab is a humanized anti-PD-1 IgG4 antibody which blocks the binding of PD1 to its ligands PD-L1 and PD-L2.

DRUG

Investigator choice of chemotherapy

Commonly used chemotherapy as per investigator's choice. The dose and route of administration was the one described in each drug's label.

Trial Locations (18)

10002

Novartis Investigative Site, Taipei

10016

NYU Laura and Isaac Perlmutter Cancer Center Laura & Isaac Perlmutter Ctr, New York

10330

Novartis Investigative Site, Bangkok

22031

Virginia Cancer Specialists, Fairfax

30060

Northwest Georgia Oncology Center NWGA Onc - Carrollton, Marietta

33305

Novartis Investigative Site, Taoyuan District

48201

Karmanos Cancer Institute, Detroit

50200

Novartis Investigative Site, Chiang Mai

70403

Novartis Investigative Site, Tainan City

83301

Novartis Investigative Site, Kaohsiung City

90110

Novartis Investigative Site, Songkhla

94800

Novartis Investigative Site, Villejuif

169610

Novartis Investigative Site, Singapore

510060

Novartis Investigative Site, Guangzhou

06189

Novartis Investigative Site, Nice

Unknown

Novartis Investigative Site, Hong Kong

Novartis Investigative Site, Kowloon

Novartis Investigative Site, Tuenmen

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY