Bruno Strigini

Novartis confirms benefits of first-line Tasigna treatment seen in earlier trials in newly-diagnosed patients with chronic myeloid leukemia (CML)

Patients on Tasigna achieved rapid and high rates of molecular response with a very low rate of progression to advanced…

9 years ago

20th EHA Congress in Vienna: Novartis data shows increased PFS benefit of Farydak® in new subgroup of patients with previously treated multiple myeloma

Panobinostat combination more than doubled median PFS benefit by 7.8 months in patients who received >=2 prior lines of therapy,…

9 years ago

Novartis: US FDA approved Promacta for the treatment of children six years and older with chronic immune thrombocytopenia (ITP)

Promacta® (eltrombopag) significantly increased and sustained platelet counts in two studies, including the largest Phase III clinical trial in this…

9 years ago

Novartis’s Signifor® LAR to treat patients with life-threatening hormonal disorder acromegaly receives FDA approval

Acromegaly is an endocrine disorder caused by elevated growth hormone (GH) and insulin-like growth factor-1 (IGF-1) levels[1] Signifor LAR, a…

9 years ago

Novartis’ Signifor® (pasireotide) intramuscular injection to treat adult patients with acromegaly approved by the European Commission

Acromegaly is a rare pituitary disorder, which requires normalization of hormonal levels to help prevent the serious consequences of the…

9 years ago