PubMed Journals Articles About "Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia" RSS

19:31 EDT 18th March 2018 | BioPortfolio

Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia PubMed articles on BioPortfolio. Our PubMed references draw on over 21 million records from the medical literature. Here you can see the latest Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia articles that have been published worldwide.

More Information about "Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia" on BioPortfolio

We have published hundreds of Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia news stories on BioPortfolio along with dozens of Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia Clinical Trials and PubMed Articles about Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia Companies in our database. You can also find out about relevant Genehmigt Erweiterte Indikation Novartis Krebsmittel Zykadia Drugs and Medications on this site too.

Showing "genehmigt erweiterte Indikation Novartis Krebsmittel Zykadia" PubMed Articles, all 9

Erfahrungen am Lebensende: Eine Umfrage bei Ärzten und Pflegenden eines Spitals für anthroposophisch erweiterte Medizin.

Google, Novartis back Medicxi's ambitions.

First approval in sight for Novartis' CAR-T therapy after panel vote.

Novartis trial validates inflammasome as chronic disease driver.

Patent trend and competitive analysis of cancer immunotherapy in the United States.

Immunotherapy has brought high hopes for cancer treatment, and attracted tremendous resources from the biopharmaceutical community. Here we analyze cancer immunotherapy-related patents granted by the United States Patent and Trademark Office in the past decade (2006-2016). A total of 2,229 patents were identified in 13 subfields. The growth of patent number in this field has outpaced the background rate, with cytokine-related therapies, immune checkpoint inhibitors, and natural killer cell therapies growing...

A guide to manufacturing CAR T cell therapies.

In recent years, chimeric antigen receptor (CAR) modified T cells have been used as a treatment for haematological malignancies in several phase I and II trials and with Kymriah of Novartis and Yescarta of KITE Pharma, the first CAR T cell therapy products have been approved. Promising clinical outcomes have yet been tempered by the fact that many therapies may be prohibitively expensive to manufacture. The process is not yet defined, far from being standardised and often requires extensive manual handling ...

Continuous manufacturing of co-crystals: challenges and prospects.

The last decade has witnessed extensive growth in the field of co-crystallization for mitigating the solubility and dissolution-related issues of poorly soluble drugs. This is largely because co-crystals can modify the physicochemical properties of drugs without any covalent modification in the drug molecules. The US Food and Drug Administration (FDA) now considers drug products that are designed to contain a new co-crystal, analogous to new polymorph of the active pharmaceutical ingredient (API). This posi...

Perspectives from the Patient and the Healthcare Professional in Multiple Sclerosis: Social Media and Participatory Medicine.

When faced with a diagnosis of multiple sclerosis (MS), patients often turn to the Internet and social media to find support groups, read about the experiences of other people affected by MS and seek their advice, and research their condition and treatment options to discuss with their healthcare professionals (HCPs). Here, we examine the use of social media and the Internet among patients with MS, considering its impact on patient empowerment and patient participation in treatment decision-making and MS re...

Ethics approval in applications for open-access clinical trial data: An analysis of researcher statements to

Although there are a number of online platforms for patient-level clinical trial data sharing from industry sponsors, they are not very harmonized regarding the role of local ethics approval in the research proposal review process. The first and largest of these platforms is (CSDR), which includes over three thousand trials from thirteen sponsors including GlaxoSmithKline, Novartis, Roche, Sanofi, and Bayer. CSDR asks applicants to state whether they have received ethics approva...

Quick Search