AZD1775 Continued Access Study to Assess Safety and Tolerability for Patients Enrolled in AZD1775 Clinical Pharmacology Studies

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

October 27, 2017

Primary Completion Date

May 17, 2019

Study Completion Date

May 17, 2019

Conditions
Solid Tumors
Interventions
DRUG

Wee-1 kinase inhibitor AZD1775

Patients will receive AZD1775 300 mg orally once daily. Days 1 to 5 and 8 to 12 of a 21 day cycle (ie, 5 days on and 2 days off for Weeks 1 and 2 of a 21-day cycle). All patients must receive a serotonin receptor 3 (5-HT3) antagonist, ondansetron (Zofran) 8 mg orally/IV or granisetron (Kytril) 1 mg orally/IV prior to each dose of AZD1775. Dexamethasone 4 mg orally/IV will be given with each AZD1775 dose at a minimum on the first day of dosing of AZD1775 of every 5 day dosing period, unless contraindicated or not well-tolerated.

Trial Locations (14)

29605

Research Site, Greenville

33075

Research Site, Bordeaux

44805

Research Site, Saint-Herblain

45229

Research Site, Cincinnati

48025

Research Site, Bingham Farms

48202

Research Site, Detroit

75251

Research Site, Dallas

03756

Research Site, Lebanon

02903

Research Site, Providence

1066 CX

Research Site, Amsterdam

1081 HV

Research Site, Amsterdam

6202 AZ

Research Site, Maastricht

G12 0YN

Research Site, Glasgow

M20 4BX

Research Site, Manchester

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Quintiles, Inc.

INDUSTRY

lead

AstraZeneca

INDUSTRY