Exchange: NASDAQ·Updated 07:30 PM EDT
EXEL logo

EXEL Exelixis Inc

$60.62
$0.84
(1.42%)
Today
Closed $59.86
$0.76
(1.27%)
After Hours
EarningsOct 27
Mkt Cap$14.62B
Vol2.67M

About EXEL

Exelixis, Inc. is an oncology company, which focuses on discovering, developing, and commercialization of new medicines for difficult-to-treat cancers. Its products include cabometyx, cometriq, and cotellic. The company was founded by Stelios Papadopoulos on November 15, 1994, and is headquartered in Alameda, CA.
50

Neutral Sentiment

How do you feel about EXEL?

Jimmy34
$EXEL this request doesn’t affect the approval of the drug it generally speaking it just extends the breath of the label for the drug It’s not a negative it’s actually a positive it’s gonna lead to an approval with extending the breath of the label based upon side effects
1
Johnnyf22
$EXEL big time rug pull underway. Big boys ran it up till noon today to unload shares. Big sell off. Not sure if news just hit or or whether it’s just algos. Hard for breakouts to work however with the changing policies minute by minute by this admin every day. Hopefully this admin will stop being so volatile so the stock market can stop being so volatile. They go hand in hand.
StocktwitsNews
EXEL Stock Slides After FDA Adds Three Months To Cancer Drug Review — William Blair Sees More Swings In Near Term $EXEL $IJH $VTI https://stocktwits.com/news/equity/markets/exel-stock-slides-after-fda-adds-three-months-to-cancer-drug-review-william-blair-sees-more-swings-in-near-term/cZtXM0eRBbg
DonCorleone77
$EXEL Exelixis says FDA extends review period for zanzalintinib NDA by three months Exelixis announced that on September 10, the U.S. Food and Drug Administration notified Exelixis that it had extended the review period for Exelixis' new drug application for zanzalintinib, in combination with atezolizumab, for the treatment of patients with metastatic colorectal cancer by three months. In response to an FDA information request, Exelixis had submitted updated safety and efficacy data, which the FDA has deemed a major amendment. The updated Prescription Drug User Fee Act action date is March 3, 2027.

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