Phase II Study of the Optimal Scheme of Administration of Pazopanib in Thyroid Carcinoma

PHASE2CompletedINTERVENTIONAL
Enrollment

168

Participants

Timeline

Start Date

March 31, 2013

Primary Completion Date

January 31, 2019

Study Completion Date

January 31, 2019

Conditions
Thyroid Carcinoma
Interventions
DRUG

Continuous pazopanib (Arm A)

Daily oral administration of pazopanib 800mg (28 days cycles) from randomization until progression (according to RECIST 1.1) under treatment, after an initial period of 6 cycles (28 days) of daily administration of pazopanib 800mg from inclusion until randomization

DRUG

Intermittent pazopanib (Arm B)

"Temporary discontinuation of pazopanib at randomization, after an initial period of 6 cycles (28 days) of daily administration of pazopanib 800mg from inclusion until randomization. Pazopanib will be reintroduced for 6 cycles of 28 days, with daily administration of pazopanib 800mg, as soon as the patient relapses (progressive disease according to RECIST 1.1). At the end of this additional 6 cycles, study drug will be stopped a second time.~This sequential scheme will be maintained until the patient experiences on-treatment progression"

Trial Locations (13)

13385

Hôpital de la Timone APHM, Marseille

14076

Centre François Baclesse, Caen

31052

Institut Claudius Régaud, Toulouse

33075

CHU Bordeaux, Bordeaux

33076

Institut Bergonié, Bordeaux

49933

CHU Angers, Angers

51726

Institut Jean Godinot, Reims

59037

CHRU Lille Hôpital Claude Huriez, Lille

69373

Centre Leon Berard, Lyon

75010

Hôpital Saint-Louis APHP, Paris

75651

Hôpital de la Pitié Salpêtrière APHP, Paris

94805

Institut Gustave Roussy, Villejuif

06189

Centre Antoine Lacassagne, Nice

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Centre Leon Berard

OTHER

NCT01813136 - Phase II Study of the Optimal Scheme of Administration of Pazopanib in Thyroid Carcinoma | Biotech Hunter | Biotech Hunter