A Safety and Efficacy Study of CC-90011 in Participants With Relapsed and/or Refractory Solid Tumors and Non-Hodgkin's Lymphomas

PHASE1TerminatedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

August 31, 2016

Primary Completion Date

March 25, 2024

Study Completion Date

March 25, 2024

Conditions
Lymphoma, Non-HodgkinNeoplasms
Interventions
DRUG

CC-90011

Specified dose on specified days

DRUG

Rifampicin

Specified dose on specified days

DRUG

Itraconazole

Specified dose on specified days

Trial Locations (15)

13273

Local Institution - 102, Marseille

20133

Local Institution - 201, Milan

20141

Local Institution - 202, Milan

21079

Local Institution - 101, Dijon

28040

Local Institution - 402, Madrid

28041

Local Institution - 404, Madrid

39008

Local Institution - 401, Santander

40123

Local Institution - 200, Bologna

94805

Local Institution - 100, Villejuif

104-0045

Local Institution - 501, Chuo-ku

135-8550

Local Institution - 502, Koto-Ku

277-8577

Local Institution - 500, Kashiwa

08035

Local Institution - 400, Barcelona

SW3 6JJ

Local Institution - 300, London

NE7 7DN

Local Institution - 301, Newcastle upon Tyne

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celgene

INDUSTRY