Follow-up Study for Patients Who Completed Study ALX0681-C301 (Post-HERCULES)

PHASE3CompletedINTERVENTIONAL
Enrollment

104

Participants

Timeline

Start Date

October 6, 2016

Primary Completion Date

October 23, 2020

Study Completion Date

October 23, 2020

Conditions
Acquired Thrombotic Thrombocytopenic Purpura
Interventions
BIOLOGICAL

Caplacizumab

OTHER

Standard of Care

• PE with plasma (e.g., fresh frozen plasma, solvent detergent/viral-inactivated plasma, cryosupernatant), • Corticosteroid treatment and • Use of other immunosuppressive agents (e.g., rituximab).

Trial Locations (45)

10595

Investigator site, Valhalla

15232

Investigator site, Pittsburgh

27710

Investigator Site, Durham

27834

Investigator site, Greenville

29425

Investigator Site, Charleston

43210

Investigator Site, Columbus

63110

Investigator site, St Louis

73104

Investigator Site, Oklahoma City

Unknown

Investigator site, Vienna

Investigator site, Antwerp

Investigator site, Brussels

Investigator site, La Louvière

Investigator site, Leuven

Investigator Site, Halifax

Investigator Site, Québec

Investigator Site, Toronto

Investigator Site, Brno

Investigator Site, Olomouc

Investigator site, Caen

Investigator site, Lille

Investigator site, Marseille

Investigator site 1, Paris

Investigator site 2, Paris

Investigator Site, Budapest

Investigator Site, Debrecen

Investigator Site, Haifa

Investigator Site, Jerusalem Region

Investigator Site, Nahariya

Investigator Site, Catania

Investigator Site, Milan

Investigator site, Pesaro

Investigator Site, Rome

Investigator Site, Vicenza

Investigator Site 1, Barcelona

Investigator Site 2, Barcelona

Investigator site, Seville

Investigator Site 2, Valencia

Investyigator Site 1, Valencia

Investigator site, Bern

Investigator site, Ankara

Investigator site, Istanbul

Investigator site, Kayseri

Investigator Site, Bristol

Investigator site, Liverpool

Investigator Site, London

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY

NCT02878603 - Follow-up Study for Patients Who Completed Study ALX0681-C301 (Post-HERCULES) | Biotech Hunter | Biotech Hunter