Treat_CCM: Propranolol in Familial Cerebral Cavernous Malformation

PHASE2CompletedINTERVENTIONAL
Enrollment

71

Participants

Timeline

Start Date

April 11, 2018

Primary Completion Date

October 31, 2021

Study Completion Date

December 31, 2021

Conditions
Cerebral Cavernous Malformation
Interventions
DRUG

Propranolol

Patients randomized to the experimental arm will receive propranolol on top of standard recommended treatment for CCM. Initial oral dose of 40 mg bid will be uptitrated to 80 mg bid in the absence of excessive bradycardia or hypotension. Doses as low as 10 mg bid and up to 160 mg bid, 20 to 320mg daily, are acceptable according to tolerability.

Trial Locations (6)

20122

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan

20133

Fond. IRCCS Ist. Naz. Neurologico Carlo Besta, Milan

20162

ASST Grande Ospedale Metropolitano Niguarda, Milan

71013

IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo

98124

"IRCCS Centro Neurolesi Bonino Pulejo", Messina

00168

"Fondazione Policlinico Universitario A. Gemelli", Roma

All Listed Sponsors
collaborator

IFOM ETS - The AIRC Institute of Molecular Oncology

OTHER

lead

Mario Negri Institute for Pharmacological Research

OTHER

NCT03589014 - Treat_CCM: Propranolol in Familial Cerebral Cavernous Malformation | Biotech Hunter | Biotech Hunter