ITF2357 was discovered at Italfarmaco of Milan, Italy. It was patented in 1997 and first described in the scientific literature in 2005.
Adverse effects
In clinical trials of givinostat as a salvage therapy for advanced Hodgkin's lymphoma, the most common adverse reactions were fatigue (seen in 50% of participants), mild diarrhea or abdominal pain (40% of participants), moderate thrombocytopenia (decreased platelet counts, seen in one third of patients), and mild leukopenia (a decrease in white blood cell levels, seen in 30% of patients). One-fifth of patients experienced prolongation of the QT interval, a measure of electrical conduction in the heart, severe enough to warrant temporary suspension of treatment.
Distrofia di Duchenne, i dati sulla molecola italiana givinostat
Intervista al Prof. Pier Lorenzo Puri, Professore di pediatria, Università della California a Los Angeles (UCLA)
published: 21 Feb 2016
Webinar - Risultati dello studio clinico con Givinostat nella BMD
Registrazione del webinar del 27 ottobre 2021, nel quale si è parlato dei risultati dello studio clinico di fase 2 con givinostat nella distrofia muscolare di Becker. Ad illustrare i risultati emersi dallo studio e a rispondere alle domande di pazienti e famiglie, il Prof. Giacomo Comi, responsabile del trial presso il Policlinico di Milano.
On April 22, 2020, Italfarmaco joined Parent Project Muscular Dystrophy for a webinar to update the community about Italfarmaco's development of Givinostat and the recent results of the futility analysis of the enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
published: 27 Apr 2020
[Webinar] Italfarmaco Provides Givinostat Update - January 2018
Italfarmaco joined PPMD for a webinar on January 24, 2018 to update the Duchenne community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
published: 30 Jan 2018
[Webinar] Italfarmaco Provides Givinostat Update - March 2019
Italfarmaco joined PPMD for a webinar on March 27, 2019 to update the community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Registrazione del webinar del 27 ottobre 2021, nel quale si è parlato dei risultati dello studio clinico di fase 2 con givinostat nella distrofia muscolare di B...
Registrazione del webinar del 27 ottobre 2021, nel quale si è parlato dei risultati dello studio clinico di fase 2 con givinostat nella distrofia muscolare di Becker. Ad illustrare i risultati emersi dallo studio e a rispondere alle domande di pazienti e famiglie, il Prof. Giacomo Comi, responsabile del trial presso il Policlinico di Milano.
Registrazione del webinar del 27 ottobre 2021, nel quale si è parlato dei risultati dello studio clinico di fase 2 con givinostat nella distrofia muscolare di Becker. Ad illustrare i risultati emersi dallo studio e a rispondere alle domande di pazienti e famiglie, il Prof. Giacomo Comi, responsabile del trial presso il Policlinico di Milano.
On April 22, 2020, Italfarmaco joined Parent Project Muscular Dystrophy for a webinar to update the community about Italfarmaco's development of Givinostat and ...
On April 22, 2020, Italfarmaco joined Parent Project Muscular Dystrophy for a webinar to update the community about Italfarmaco's development of Givinostat and the recent results of the futility analysis of the enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
On April 22, 2020, Italfarmaco joined Parent Project Muscular Dystrophy for a webinar to update the community about Italfarmaco's development of Givinostat and the recent results of the futility analysis of the enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Italfarmaco joined PPMD for a webinar on January 24, 2018 to update the Duchenne community about Italfarmaco's development of Givinostat and currently enrolling...
Italfarmaco joined PPMD for a webinar on January 24, 2018 to update the Duchenne community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Italfarmaco joined PPMD for a webinar on January 24, 2018 to update the Duchenne community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Italfarmaco joined PPMD for a webinar on March 27, 2019 to update the community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 co...
Italfarmaco joined PPMD for a webinar on March 27, 2019 to update the community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Italfarmaco joined PPMD for a webinar on March 27, 2019 to update the community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Registrazione del webinar del 27 ottobre 2021, nel quale si è parlato dei risultati dello studio clinico di fase 2 con givinostat nella distrofia muscolare di Becker. Ad illustrare i risultati emersi dallo studio e a rispondere alle domande di pazienti e famiglie, il Prof. Giacomo Comi, responsabile del trial presso il Policlinico di Milano.
On April 22, 2020, Italfarmaco joined Parent Project Muscular Dystrophy for a webinar to update the community about Italfarmaco's development of Givinostat and the recent results of the futility analysis of the enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Italfarmaco joined PPMD for a webinar on January 24, 2018 to update the Duchenne community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
Italfarmaco joined PPMD for a webinar on March 27, 2019 to update the community about Italfarmaco's development of Givinostat and currently enrolling Phase 3 confirmatory study in Duchenne muscular dystrophy.
ITF2357 was discovered at Italfarmaco of Milan, Italy. It was patented in 1997 and first described in the scientific literature in 2005.
Adverse effects
In clinical trials of givinostat as a salvage therapy for advanced Hodgkin's lymphoma, the most common adverse reactions were fatigue (seen in 50% of participants), mild diarrhea or abdominal pain (40% of participants), moderate thrombocytopenia (decreased platelet counts, seen in one third of patients), and mild leukopenia (a decrease in white blood cell levels, seen in 30% of patients). One-fifth of patients experienced prolongation of the QT interval, a measure of electrical conduction in the heart, severe enough to warrant temporary suspension of treatment.
commercial launch of DUVYZAT™ (givinostat), a histone deacetylase inhibitor, for the treatment of patients six years of age and older with Duchenne muscular dystrophy (DMD) ... About DUVYZAT™ (givinostat).