
This year, despite external pressures like the Russian war on Ukraine and COVID-19 fears, major deals in the healthcare and…
The Durezol brand and generic had U.S. sales of approximately $40 million MAT for the most recent twelve months ending in…
Meanwhile, revenues during the quarter were up by 27 per cent to Rs 6,770 crore compared to Rs 5,319.7 crore…
Higher 39% YoY driven by on-going clinical trials on a respiratory asset and other developmental efforts continuing including biosimilars, it…
According to GlobalData’s Pharma Intelligence Center,13 homegrown vaccines have been approved for use against COVID-19 in China.
Studies show that heart failure claims more than 17.9 million lives every year globally whilst, medicines for critically ill heart…
According to the company’s statement, its margin on earnings before interest, taxes, depreciation, and amortisation slipped to 35 percent from…
The announcement comes after Sandoz successfully completed the acquisition of GSK’s global cephalosporins portfolio in October 2021.
Since these are not isolated incidents WHO calls on various key stakeholders engaged in the medical supply chain to take…
The drug is already being marketed in the EU, the US, and Australia.
Lilly said the FDA had sent it a complete response letter for donanemab, an antibody designed to remove amyloid protein…
Earlier this week, Novartis’ heart failure drug which is a combination of sacubitril and valsartan lost its patent.
The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Calquence Capsules, 100 mg, of AstraZeneca.
The company also informed that its rituximab biosimilar has already been approved for marketing in India and over 25 emerging…
Studies show that in India, Heart Failure remains one of the most prevalent causes of death in patients suffering from…
Reportedly, the programme is aimed at increasing access to innovative treatments in some of the world’s poorest countries.
According to the analyst consensus forecast on the GlobalData Pharma Intelligence Center, the drug is expected to reach $438 million…
Leqembi is the second anti-Aβ mAb approved by the FDA for the treatment of Alzheimer’s Disease, following the FDA’s controversial…