48
Participants
Start Date
June 24, 2024
Primary Completion Date
August 31, 2027
Study Completion Date
August 31, 2027
KVD900 150 mg
KVD900 Tablet 150 mg (2 x 75 mg)
KVD900 300 mg
KVD900 Tablet 300 mg (1 x 300 mg)
KVD900 600 mg
KVD900 Tablet 600 mg (2 x 300 mg)
COMPLETED
KalVista Investigative Site, Marseille
COMPLETED
KalVista Investigative Site, Hershey
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Milan
RECRUITING
KalVista Investigative Site, Wheaton
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Haifa
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Padua
RECRUITING
KalVista Investigative Site, Birmingham
COMPLETED
KalVista Investigative Site, Toledo
RECRUITING
KalVista Investigative Site, Evansville
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Lille
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Frankfurt am Main
COMPLETED
KalVista Investigative Site, Frankfurt am Main
RECRUITING
KalVista Investigative Site, St Louis
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Paris
COMPLETED
KalVista Investigative Site, Dallas
RECRUITING
KalVista Investigative Site, Scottsdale
RECRUITING
KalVista Investigative Site, Santa Monica
RECRUITING
KalVista Investigative Site, San Diego
COMPLETED
KalVista Investigative Site, Petah Tikva
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Tel Aviv
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Edmonton
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Rome
COMPLETED
KalVista Investigative Site, Kawagoe
ACTIVE_NOT_RECRUITING
KalVista Investigative Site, Tokyo
Lead Sponsor
KalVista Pharmaceuticals, Ltd.
INDUSTRY