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DewDiligence

06/05/19 1:40 PM

#225182 RE: DewDiligence #225158

ASCO post-mortem from Vantage—MRTX was one of the biggest winners without even presenting anything!

https://www.evaluate.com/vantage/articles/events/conferences/asco-2019-event-analyser-low-key-meeting-belies-some-huge-stock
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DewDiligence

01/07/20 9:55 AM

#228018 RE: DewDiligence #225158

MRTX—(-14%)—bolsters senior management, making a buyout somewhat less likely:

https://finance.yahoo.com/news/mirati-therapeutics-announces-executive-management-213000230.html.
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DewDiligence

05/28/21 1:47 PM

#238182 RE: DewDiligence #225158

AMGN—FDA approves Lumakras—(f/k/a AMG-510)—for_second-line KRAS-mutated NSCLC:

https://finance.yahoo.com/news/fda-approves-lumakras-sotorasib-first-164700884.html

Amgen today announced that the U.S. Food and Drug Administration (FDA) has approved LUMAKRAS (sotorasib) for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC), as determined by an FDA-approved test, who have received at least one prior systemic therapy.

LUMAKRAS has received accelerated approval based on overall response rate (ORR) and duration of response (DoR). Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

The next goal for AMGN is to obtain approval in the first-line setting.