Investigating Safety, Tolerability and Efficacy of AZD5363 When Combined With Paclitaxel in Breast Cancer Patients

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

148

Participants

Timeline

Start Date

October 3, 2012

Primary Completion Date

January 28, 2017

Study Completion Date

October 3, 2022

Conditions
Advanced or Metastatic Breast CancerER+ve Advanced or Metastatic Breast Cancer
Interventions
DRUG

AZD5363 when combined with weekly paclitaxel.

AZD5363: oral capsule, twice daily in a weekly 2 days on-treatment, 5 days-off, schedule. Treatment to begin the day following the first dose of paclitaxel and to continue until treatment withdrawal. Paclitaxel: intravenously once a week. AZD5363 and paclitaxel will be received for 3 consecutive weeks, followed by one week off-therapy in 4-week cycles.

DRUG

AZD5363 when combined with weekly paclitaxel.

AZD5363: oral capsule, twice daily in a weekly 4 days on-treatment, 3 days-off, schedule. Treatment to begin the day following the first dose of paclitaxel and to continue until treatment withdrawal. Paclitaxel: intravenously once a week. AZD5363 and paclitaxel will be received for 3 consecutive weeks, followed by one week off-therapy in 4-week cycles.

DRUG

AZD5363when combined with weekly paclitaxel.

Either a 2/5 or 3/4 intermittent dosing schedule of AZD5363 based on the outcome of Part A. Dosage: oral formulation, twice daily. Treatment to begin the day following the first dose of paclitaxel and to continue until treatment withdrawal. Paclitaxel: intravenously once a week. AZD5363 and paclitaxel will be received for 3 consecutive weeks, followed by one week off-therapy in 4-week cycles.

DRUG

A placebo in combination with weekly paclitaxel.

Either a 2/5 or 3/4 intermittent dosing schedule of placebo matched to AZD5363 based on the outcome of Part A. Dosage: oral formulation, twice daily. Treatment to begin the day following the first dose of paclitaxel and to continue until treatment withdrawal. Paclitaxel: intravenously once a week. placebo and paclitaxel will be received for 3 consecutive weeks, followed by one week off-therapy in 4-week cycles.

Trial Locations (41)

1330

Research Site, Sofia

4004

Research Site, Plovdiv

7000

Research Site, Juchitán

13620

Research Site, Seongnam-si

15036

Research Site, Lima

15046

Research Site, Miraflores

28040

Research Site, Madrid

28041

Research Site, Madrid

29010

Research Site, Málaga

46010

Research Site, Valencia

50080

Research Site, Estado de México

64460

Research Site, Monterrey

68000

Research Site, Oaxaca City

69310

Research Site, Pierre-Bénite

75248

Research Site, Paris

94805

Research Site, Villejuif

119228

Research Site, Singapore

T2N 4N2

Research Site, Calgary

K1H 8L6

Research Site, Ottawa

H4A 3T2

Research Site, Montreal

G1S 4L8

Research Site, Québec

656 53

Research Site, Brno

260-8717

Research Site, Chiba

104-0045

Research Site, Chūōku

811-1395

Research Site, Fukuoka

181-8611

Research Site, Mitaka-shi

540-0006

Research Site, Osaka

870-0854

Research Site, Ōita

L 41

Research Site, Lima

LIMA 27

Research Site, Lima

03080

Research Site, Seoul

03722

Research Site, Seoul

135-710

Research Site, Seoul

08025

Research Site, Barcelona

08035

Research Site, Madrid

G12 0YN

Research Site, Glasgow

LE1 5WW

Research Site, Leicester

SW3 6JJ

Research Site, London

M20 4BX

Research Site, Manchester

PL6 8DH.

Research Site, Plymouth

SM2 5PT

Research Site, Sutton

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY