Efficacy of Thalidomide in the Treatment of Hereditary Hemorrhagic Telangiectasia

PHASE2CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

November 30, 2011

Primary Completion Date

October 31, 2014

Study Completion Date

October 11, 2016

Conditions
Hereditary Hemorrhagic TelangiectasiaEpistaxis
Interventions
DRUG

Thalidomide

"Eligible patients will receive thalidomide at a starting dose of 50 mg/day by mouth at bedtime for 4 weeks. In the event of unsatisfactory/no response, thalidomide dosage will be progressively increased by 50 mg/day every 4 weeks until complete or partial response, to a maximum dose of 200 mg/day.~Treatment will be continued until one of the following criteria is met:~* 8 additional weeks of treatment after the achievement of complete response~* 16 additional weeks of treatment after the achievement of partial response~* 24 weeks of treatment completed without response~* unacceptable toxicity. Then, patients will be followed off of thalidomide for 24 weeks."

Trial Locations (1)

27100

Clinica Medica 3, Fondazione IRCCS Policlinico S. Matteo, Pavia

All Listed Sponsors
lead

Fondazione IRCCS Policlinico San Matteo di Pavia

OTHER

NCT01485224 - Efficacy of Thalidomide in the Treatment of Hereditary Hemorrhagic Telangiectasia | Biotech Hunter | Biotech Hunter