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1. Biologie
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1.1 Biologie - Gènes
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3.1 Tabac
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Working Together Around The World To Kick The Big Tobacco Habit [Health Affairs Blog]
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To
further support countries and public health officials in their battle
against the tobacco epidemic, WHO created the technical package called
MPOWER. The acronym stands for a group of policies proven to reduce
tobacco use: Monitor tobacco use; Protect people from second-hand smoke;
Offer help to quit; Warn about dangers of tobacco use; Enforce
advertising bans; and Raise tobacco taxes.
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4.12 Biopsies liquides
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Company Will Raise $1 Billion To Create Blood Test To Detect Cancer [Forbes]
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As
part of the announcement, Grail is also spinning out of its parent
company, San Diego's Illumina, the $2.4 billion (sales) firm that makes
most of the DNA sequencing machines that scientists and doctors use to
study human biology, diagnose rare genetic diseases, and pick treatments
for cancer patients.
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4.9 Dép., diag. & prono. - Sein
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Mammogram Record Retention: FDA Offers Guidance [RAPS]
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Following
some confusion over mammogram record retention requirements, the US
Food and Drug Administration (FDA) on Thursday told all facilities
conducting such tests that they must retain a record of each one for at
least five years, or not less than 10 years if no additional mammograms
of the patient are performed at the facility (or a longer period if
mandated by state or local law).
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5. Traitements
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Nanoparticles awaken immune cells to fight cancer [Science]
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This
time their nanoparticles didn’t contain any additional chemotherapeutic
drug. They then blasted the tumors with infrared light, and waited for
the results. And in almost every case, not only was the primary breast
cancer tumor destroyed, but metastases in the lung were wiped out as
well.
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5.12.1 Immunothérapies - partenariats
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5.2 Pharma
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What Passes For Positive Data [In the Pipeline]
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This
is cherry-picking no matter how you look at it, and Adam Feuerstein was
right to call it “shameful conduct” to press-release it the way the
company did. But hey, the stock bounced (or it has so far this morning),
and that’s what matters, right?
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5.3 Traitements - FDA, EMA, NICE...
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European Commission Clears up Questions on Orphan Drug Regulation [RAPS]
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To
qualify for orphan designation, a medicine must treat, diagnose or
prevent a serious or life threatening condition that affects fewer than 5
in 10,000 people in the European Union. Additionally, there must not be
any "satisfactory" treatment for the condition within the EU, or the
medicine must be shown to demonstrate significant benefit to patients
over existing options.
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6.1 Observation
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6.5 Médecines alternatives
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