A Dose Finding and Safety Study of CC-220, Alone and in Combination With an Anti-CD20 Monoclonal Antibody (mAb) in Subjects With Relapsed or Refractory Lymphomas

PHASE1TerminatedINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

November 11, 2020

Primary Completion Date

January 31, 2023

Study Completion Date

January 9, 2025

Conditions
Lymphoma
Interventions
DRUG

CC-220

Oral

DRUG

Rituximab

SC and IV infusion

DRUG

Obinutuzumab

IV Infusion

Trial Locations (26)

4103

Local Institution - 402, Leipzig

5505

Local Institution - 500, Seoul

10065

Local Institution - 100, New York

12203

Local Institution - 401, Berlin

14642

University of Rochester Cancer Center, Rochester

20133

Local Institution - 303, Milan

25123

Local Institution - 300, Brescia

27100

Local Institution - 301, Pavia

32746

Local Institution - 105, Lake Mary

33305

Local Institution - 601, Taoyuan

33604

Local Institution - 205, Pessac

34295

Local Institution - 201, Montpellier

37134

Local Institution - 302, Verona

37203

Local Institution - 103, Nashville

40447

Local Institution - 602, Taoyuan

44093

Local Institution - 202, Nantes

48149

Local Institution - 403, Münster

55905

Local Institution - 102, Rochester

59037

Local Institution - 200, Lillie Cedex

75010

Local Institution - 204, Paris

83301

Local Institution - 600, Niaosong District Kaohsiung City

85054

Local Institution - 106, Phoenix

94010

Local Institution - 203, Créteil

97080

Local Institution - 404, Würzburg

03722

Local Institution - 502, Seoul

06351

Local Institution - 501, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celgene

INDUSTRY

NCT04464798 - A Dose Finding and Safety Study of CC-220, Alone and in Combination With an Anti-CD20 Monoclonal Antibody (mAb) in Subjects With Relapsed or Refractory Lymphomas | Biotech Hunter | Biotech Hunter