Report of Foreign Issuer (6-k)
March 19 2019 - 10:17AM
Edgar (US Regulatory)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
6-K
REPORT OF
FOREIGN PRIVATE ISSUER
PURSUANT TO RULE
13a-16
OR
15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934
For the month of March 2019
Commission File Number:
001-31368
SANOFI
(Translation of
registrants name into English)
54, rue La
Boétie, 75008 Paris, FRANCE
(Address of principal executive offices)
Indicate by check mark whether the registrant files or will file annual reports under cover Form
20-F
or Form
40-F.
Form
20-F ☒ Form
40-F ☐
Indicate by check mark if the registrant is submitting the Form
6-K
in paper as permitted by
Regulation
S-T
Rule 101(b)(1): ☐
Indicate by check mark if the registrant is
submitting the Form
6-K
in paper as permitted by Regulation
S-T
Rule 101(b)(7): ☐
Indicate by check mark whether the registrant by furnishing the information contained in this Form is also thereby furnishing the information
to the Commission pursuant to Rule
12g3-2(b)
under the Securities Exchange Act of 1934.
Yes ☐ No ☒
If Yes marked, indicate below the file number assigned to the registrant in connection with Rule
12g3-2(b):
82-
In March 2019, Sanofi issued the press releases attached hereto as Exhibit 99.1, 99.2, 99.3 and 99.4 which
are incorporated herein by reference.
Exhibit List
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Exhibit
No.
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Description
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Exhibit 99.1
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Press release dated March 15, 2019: Praluent® (alirocumab) now approved in European Union to reduce the risk of cardiovascular events in patients with established cardiovascular disease
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Exhibit 99.2
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Press release dated March 13, 2019:
Sanofi successfully prices EUR 2 billion of bond issues
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Exhibit 99.3
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Press release dated March 8, 2019: Filing of the 2018 U.S. Form
20-F
and French « Document de Référence » containing the Annual Financial
Report
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Exhibit 99.4
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Press release dated March 8, 2019: FDA to undertake priority review of Dupixent® (dupilumab) for adults with inadequately controlled severe chronic rhinosinusitis with nasal polyps
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2
Exhibit Index
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Exhibit
No.
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Description
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Exhibit 99.1
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Press release dated March 15, 2019: Praluent® (alirocumab) now approved in European Union to reduce the risk of cardiovascular events in patients with established cardiovascular disease
|
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Exhibit 99.2
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Press release dated March 13, 2019:
Sanofi successfully prices EUR 2 billion of bond issues
|
|
|
Exhibit 99.3
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Press release dated March 8, 2019: Filing of the 2018 U.S. Form
20-F
and French « Document de Référence » containing the Annual Financial
Report
|
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Exhibit 99.4
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Press release dated March 8, 2019: FDA to undertake priority review of Dupixent® (dupilumab) for adults with inadequately controlled severe chronic rhinosinusitis with nasal polyps
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3
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by
the undersigned, thereunto duly authorized.
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Dated: March 19, 2019
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SANOFI
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By
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/s/ Alexandra Roger
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Name:
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Alexandra Roger
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Title:
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Head of Securities Law and Capital Markets
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4
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