This final guidance was issued regarding the treatment of macular oedema caused by retinal vein occlusion (RVO) where the vein to the retina or one of its branches is blocked (central or branch retinal vein occlusion).
The agency noted its recommendation is valid only if Novartis makes ranibizumab available under terms agreed with the Department of Health as part of a patient access scheme.
Perrigo to acquire United States rights for Entocort from AstraZeneca
US FDA approves Boehringer Ingelheim's Pradaxa
Phase II clinical trial for potential treatment of androgenetic alopecia completed by Samumed
Life Sciences Partners collaborates on immuno-oncology with Bristol-Myers Squibb
Arsanis initiates first cohort in Phase one clinical trial of ASN100
Impax introduces generic Avodart (Dutasteride) Capsules, 0.5 mg
Mylan unveils generic FazaClo orally disintegrating tablets for treating schizophrenia