Sanofi (SNY)
(Delayed Data from NSDQ)
$53.10 USD
+1.90 (3.71%)
Updated Jul 25, 2024 04:00 PM ET
After-Market: $53.09 -0.01 (-0.02%) 7:58 PM ET
3-Hold of 5 3
B Value D Growth C Momentum C VGM
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$53.10 USD
+1.90 (3.71%)
Updated Jul 25, 2024 04:00 PM ET
After-Market: $53.09 -0.01 (-0.02%) 7:58 PM ET
3-Hold of 5 3
B Value D Growth C Momentum C VGM
Zacks News
Sanofi to Acquire Haemophilia Focused Bioverativ, Stock Dips
by Zacks Equity Research
Sanofi (SNY) is set to acquire blood disorder focused biopharmaceutical company, Bioverativ, for $11.6 billion.
Will These 4 Large-Cap Drug Stocks Be Big Winners This Earnings Season?
by Arpita Dutt
Here is a look at four large-cap pharma and biotech stocks including Merck (MRK) that could surpass earnings expectations in the fourth quarter.
CES 2018 Promises a Thrilling Year for Gaming Enthusiasts
by Zacks Equity Research
During CES 2018, a number of companies displayed some extravagant products which are set to change the gaming experience entirely this year.
Pharma Stock Roundup: Novo Nordisk Reveals Bid to Acquire Ablynx, Pfizer & Others at Healthcare Conference
by Arpita Dutt
Focus this week was on pipeline updates provided by several companies including Pfizer (PFE) at a healthcare conference while Novo Nordisk's bid to acquire Ablynx also made news.
Novo Nordisk's Ozempic Gets Canadian Approval for Diabetes
by Zacks Equity Research
Novo Nordisk (NVO) announced that Health Canada has approved Ozempic to improve glycemic control in adults with type II diabetes mellitus.
Emergent Down on '18 View, Posts Preliminary '17 Results
by Zacks Equity Research
Emergent (EBS) provides preliminary results for 2017 and its guidance for 2018. The results exceed management's outlook issued in November last year.
AbbVie's Upadacitinib Gains Breakthrough Therapy Designation
by Zacks Equity Research
AbbVie's (ABBV) atopic dermatitis (eczema) candidate, upadacitinib, gets breakthrough therapy status from the FDA.
Regeneron, Sanofi Expand Investment in Cemiplimab & Dupilumab
by Zacks Equity Research
Regeneron (REGN) and partner Sanofi announced that they will expand their investment for the development cemiplimab in oncology, and label expansion of dupilumab in Type II allergic diseases.
Alnylam, Sanofi Announce Restructuring Deal for RNAi Products
by Zacks Equity Research
Alnylam (ALNY) and Sanofi entered into a strategic restructuring of their RNAi therapeutics rare genetic diseases alliance.
5 Reasons to Pick Emergent as an Investment-Worthy Stock
by Zacks Equity Research
Other than a bullish rank, there are several factors that make Emergent (EBS) a solid investment in 2018.
3 Biotech and Pharma Stocks with FDA Catalysts this January
by Arpita Dutt
2017 saw the FDA approving 46 novel drugs as well as path-breaking treatments like Novartis's (NVS) Kymriah and Gilead's Yescarta. Here is a look at three companies expecting a decision this January.
Protalix (PLX) Fabry Disease Candidate Gets Orphan Status
by Zacks Equity Research
Protalix BioTherapeutics's (PLX) pipeline candidate, PRX-102, gets orphan drug status in Europe which is being developed as a treatment for Fabry disease.
BioMarin's (BMRN) Gene Therapy Enters First Phase III Study
by Zacks Equity Research
BioMarin (BMRN) commences the first phase III study to evaluate the 6e13 vg/kg dose of its investigational gene therapy, valoctocogene roxaparvovec, for severe hemophilia A.
Why is Alnylam's (ALNY) Stock Up More Than 200% This Year?
by Zacks Equity Research
Alnylam's (ALNY) share price has increased year to date based on impressive progress of its pipeline candidates.
Regeneron in Strategic Immuno-Oncology Collaboration With ISA
by Zacks Equity Research
Regeneron Pharmaceuticals (REGN) and ISA Pharmaceuticals inked an agreement to advance ISA101 in combination with cemiplimab.
Alnylam/Sanofi Submit MAA in Europe for RNAi Candidate
by Zacks Equity Research
Alnylam (ALNY) and partner Sanofi have submitted a Marketing Authorization Application to the European Medicines Agency for patisiran for the treatment adults with hereditary ATTR amyloidosis with polyneuropathy.
Novo Nordisk's (NVO) Semaglutide Gets Positive CHMP Opinion
by Zacks Equity Research
Novo Nordisk (NVO) announced that the Committee for Medicinal Products for Human Use has adopted a positive opinion recommending marketing authorisation of semaglutide for the treatment of adults with type II diabetes mellitus.
Sanofi/Alnylam Say FDA Lifts Clinical Hold on Fitusiran
by Zacks Equity Research
Sanofi (SNY) and Alnylam announced that the FDA has lifted the clinical hold placed on all ongoing studies of its hemophilia candidate, fitusiran.
Mylan Announces IPR Proceedings for Sanofi's Lantus Patents
by Zacks Equity Research
Mylan (MYL) announced that interpartes review (IPR) proceedings has been initiated by PTAB regarding two Orange Book-listed patents, U.S. Patent Nos. 7,476,652 and 7,713,930 owned by Sanofi.
Cancer Space Update: Roche, Pfizer & Regeneron Make Data Presentations
by Zacks Equity Research
Several presentations at the annual meeting of the American Society of Hematology grab headlines in the cancer space.
Pharma Stock Roundup: Teva Announces Major Job Cuts, Lilly Provides 2018 Outlook
by Arpita Dutt
This week's pharma sector highlights include ASH data, Teva's restructuring announcement and Lilly's (LLY) 2018 outlook.
Lilly Issues Guidance for 2018, New Drugs to Drive Top Line
by Zacks Equity Research
Eli Lilly (LLY) issues financial guidance for 2018 and also reaffirms the previously issued 2017 projection as well as its long-term expectations.
Regeneron, Sanofi Report Positive Top Line Skin Cancer Data
by Zacks Equity Research
Regeneron (REGN) and partner Sanofi announced positive top-line results from a pivotal phase II study of skin cancer candidate cemiplimab.
Intersect ENT (XENT) SINUVA Implant Receives FDA Approval
by Zacks Equity Research
Intersect ENT's (XENT) consistent focus on the chronic sinusitis market is likely to lend the company a competitive edge in the niche space.
Sanofi Wins FDA Approval for Biosimilar of Lilly's Humalog
by Zacks Equity Research
Sanofi's (SNY) Admelog, a follow-on biologic version of Lilly's Humalog, received FDA approval.