DFE Pharma expands its inhalation portfolio with the launch of Lactohale 400
Being a leader in Dry Powder Inhalation, DFE Pharma further expands its broad excipient portfolio of inhalation grade lactose
<br />
Drug Discovery & Development | 05/07/2022 | By Sudeep Soparkar | 897
Drug Discovery & Development | 28/06/2022 | By Sudeep Soparkar | 662
Merck opens ?59 M CDMO facility to address critical cancer therapies
The 70,000 square foot facility, officially opened, brings 50 new jobs to the area
Drug Discovery & Development | 24/06/2022 | By Sudeep Soparkar | 650
Gericke ensures precise dosing operation with high-performance feeding unit
The right selection ensures recipe consistency and automated production to prevents product rejects
Drug Discovery & Development | 16/06/2022 | By Sudeep Soparkar | 361
Drug Discovery & Development | 16/06/2022 | By Sudeep Soparkar | 795
Daiichi Sankyo's quizartinib plus chemotherapy improves OS in patients with AML
Quizartinib combined with standard induction and consolidation chemotherapy and then continued as a single agent demonstrated a 22.4 per cent reduction in the risk of death
Drug Discovery & Development | 13/06/2022 | By Sudeep Soparkar | 858
Autoimmune drug by Bristol Myers shows potential in lupus
Deucravacitinib is one of nine new drugs that Bristol Myers executives believe will help offset revenue losses
Drug Discovery & Development | 08/06/2022 | By Sudeep Soparkar | 804
PerkinElmer unveils ultrarapid whole-genome sequencing
The urWGS offering provides physicians with comprehensive, meaningful results in five days to help inform clinical management and improve outcomes
Drug Discovery & Development | 08/06/2022 | By Sudeep Soparkar | 541
BioNTech 2nd phase of Covid 19 trials completed
The vaccine, based on messenger RNA (mRNA) technology, is one of the most widely used worldwide against COVID, but has yet to receive an approval in China, which has relied only on domestically-developed vaccine
Drug Discovery & Development | 12/05/2022 | By Sudeep Soparkar | 694
US FDA approval for Incyte's Olumiant
Eli Lilly and Company and Incyte announced the US Food and Drug Administration (FDA) has approved Olumiant (baricitinib) for the treatment of Covid-19 in hospitalized adults requiring supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO) with a recommended dose of 4-mg once daily for 14 days.
Drug Discovery & Development | 12/05/2022 | By Sudeep Soparkar | 819
We use our own and third party cookies to produce statistical information and show you personalized advertising by analyzing your browsing, according to our COOKIES POLICY. If you continue visiting our Site, you accept its use.
More information: Privacy Policy