A Study of Adavosertib as Treatment for Uterine Serous Carcinoma

PHASE2CompletedINTERVENTIONAL
Enrollment

109

Participants

Timeline

Start Date

November 30, 2020

Primary Completion Date

May 23, 2022

Study Completion Date

February 7, 2023

Conditions
Uterine Serous Carcinoma
Interventions
DRUG

Adavosertib

The subjects will receive oral adavosertib 300 mg, once daily on Days 1 to 5 and Days 8 to 12 of a 21-day treatment cycle.

Trial Locations (27)

6189

Research Site, Nice

10065

Research Site, New York

10467

Research Site, The Bronx

13273

Research Site, Marseille

15009

Research Site, A Coruña

20141

Research Site, Milan

21079

Research Site, Dijon

28223

Research Site, Pozuelo de Alarcón

44805

Research Site, Saint-Herblain

52242

Research Site, Iowa City

55905

Research Site, Rochester

69495

Research Site, Pierre-Bénite

70433

Research Site, Covington

80045

Research Site, Aurora

80131

Research Site, Napoli

90048

Research Site, West Hollywood

91010

Research Site, Duarte

91505

Research Site, Burbank

92093

Research Site, La Jolla

98684

Research Site, Vancouver

99202

Research Site, Spokane

02215

Research Site, Boston

08903

Research Site, New Brunswick

M5G 2M9

Research Site, Toronto

00168

Research Site, Roma

08035

Research Site, Barcelona

08036

Research Site, Barcelona

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY