Report of Foreign Issuer (6-k)

Date : 07/16/2019 @ 2:30PM
Source : Edgar (US Regulatory)
Stock : Sanofi (PC) (SNYNF)
Quote : 89.55  0.0 (0.00%) @ 3:16PM
Sanofi (PC) share price Chart

Report of Foreign Issuer (6-k)

 

 

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 July 2019

Commission File Number: 001-31368

 

 

SANOFI

(Translation of registrant’s 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 June and July 2019, Sanofi issued the press releases attached hereto as Exhibit 99.1, 99.2, 99.3, 99.4, 99.5 and 99.6 which are incorporated herein by reference.

Exhibit List

 

Exhibit No.

  

Description

Exhibit 99.1    Press release dated July 10, 2019: Sanofi : FDA to review isatuximab as a potential treatment for relapsed/refractory multiple myeloma
Exhibit 99.2    Press release dated July 03, 2019: Sanofi : Libtayo ® (cemiplimab) approved for advanced cutaneous squamous cell carcinoma in the European Union
Exhibit 99.3    Press release dated June 28, 2019: Sanofi : CHMP recommends approval of Dupixent ® (dupilumab) for moderate-to-severe atopic dermatitis in adolescents
Exhibit 99.4    Press release dated June 27, 2019: Sanofi : FDA to review MenQuadfi, a meningococcal vaccine candidate
Exhibit 99.5    Press release dated June 26, 2019: Sanofi : FDA approves Dupixent ® (dupilumab) for chronic rhinosinusitis with nasal polyposis
Exhibit 99.6    Press release dated June 21, 2019: Sanofi and Regeneron announce positive topline Phase 2 results for IL-33 antibody in asthma

 

2


Exhibit Index

 

Exhibit No.

  

Description

Exhibit 99.1    Press release dated July 10, 2019: Sanofi : FDA to review isatuximab as a potential treatment for relapsed/refractory multiple myeloma
Exhibit 99.2    Press release dated July 03, 2019: Sanofi : Libtayo ® (cemiplimab) approved for advanced cutaneous squamous cell carcinoma in the European Union
Exhibit 99.3    Press release dated June 28, 2019: Sanofi : CHMP recommends approval of Dupixent ® (dupilumab) for moderate-to-severe atopic dermatitis in adolescents
Exhibit 99.4    Press release dated June 27, 2019: Sanofi : FDA to review MenQuadfi, a meningococcal vaccine candidate
Exhibit 99.5    Press release dated June 26, 2019: Sanofi : FDA approves Dupixent ® (dupilumab) for chronic rhinosinusitis with nasal polyposis
Exhibit 99.6    Press release dated June 21, 2019: Sanofi and Regeneron announce positive topline Phase 2 results for IL-33 antibody in asthma

 

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.

 

Dated: July 16, 2019             SANOFI
  By  

          /s/  Alexandra Roger

    Name:   Alexandra Roger
    Title:   Head of Securities Law and Capital Markets

 

4

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