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Genentech

US ophthalmic drugs market set to pass $34bn by 2025

25 July 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

Major market players across the US are upping investments in research to innovate on treatment methods and improve ophthalmic drugs action...

article

Application of LCMS in small-molecule drug development

24 August 2016 | By Chunang (Christine) Gu (Genentech), David Russell (Genentech), Peter Yehl (Genentech)

As a technology, mass spectrometry (MS) has evolved to the point where it is used throughout the drug development process. In particular, when MS is coupled with high-performance liquid chromatography (HPLC) it adds an orthogonal detection function for sample analysis and provides unique capabilities for pharmaceutical analysis, such as sensitivity,…

news

FDA approves Xolair to treat allergic asthma in children

11 July 2016 | By Victoria White, Digital Content Producer

The FDA has approved Genentech’s Xolair (omalizumab) to treat moderate to severe persistent asthma in children six to 11 years of age...

article

Mass Spectrometry: In-Depth Focus 2016

4 May 2016 | By European Pharmaceutical Review

In this Mass Spectrometry In-Depth Focus: Novel trends in glycosylation analysis of biotherapeutics by mass spectrometry; The use of mass spectrometry for the characterisation of proteins in small molecule drug discovery; Mass Spectrometry Q&A...

news

Daratumumab and atezolizumab to be evaluated in two studies

22 March 2016 | By Victoria White

The studies will assess the combination of daratumumab and atezolizumab in multiple myeloma and in solid tumour cancer...

news

FDA approves Gazyva to treat follicular lymphoma

1 March 2016 | By Victoria White

The FDA has approved Gazyva (obinutuzumab) plus bendamustine chemotherapy followed by Gazyva alone as a new treatment for people with follicular lymphoma...

news

FDA grants third venetoclax Breakthrough Therapy Designation

28 January 2016 | By Victoria White

The designation is for venetoclax in combination with HMAs for the treatment of patients with untreated AML who are ineligible to receive standard induction therapy...

news

FDA approves Tarceva (Erlotinib) tablets for specific type of lung cancer

15 May 2013 | By Astellas Pharma Inc.

The FDA also approved the cobas® EGFR Mutation Test, which was developed by Roche and validated in the pivotal EURTAC study...

news

Gilead Sciences to purchase biologics process research and clinical manufacturing facility from Genentech

8 August 2011 | By Gilead Sciences Inc

Gilead Sciences, Inc. has signed a definitive agreement...

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