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As Of Filer Filing For·On·As Docs:Size Issuer Agent 11/18/16 Sanofi 6-K 11/18/16 5:131K Donnelley … Solutions/FA |
Document/Exhibit Description Pages Size 1: 6-K Report by a Foreign Private Issuer HTML 13K 2: EX-99.1 Miscellaneous Exhibit HTML 17K 3: EX-99.2 Miscellaneous Exhibit HTML 12K 4: EX-99.3 Miscellaneous Exhibit HTML 20K 5: EX-99.4 Miscellaneous Exhibit HTML 18K
| 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 November 2016
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 October and November 2016, Sanofi issued the press releases attached hereto as Exhibit 99.1 to 99.4 which is incorporated herein by reference.
Exhibit List
| Exhibit No. |
Description | |
| Exhibit 99.1 | Press release dated October 28, 2016: Sanofi and Regeneron Receive Complete Response Letter from FDA for Sarilumab, an Investigational Treatment for Rheumatoid Arthritis | |
| Exhibit 99.2 | Press release dated November 11, 2016: Sanofi Receives CHMP Recommendation for Approval of SuliquaTM in the EU | |
| Exhibit 99.3 | Press release dated November 16, 2016: Sanofi and Regeneron Present Results from Phase 3 MONARCH Study of Investigational Sarilumab at American College of Rheumatology Annual Meeting | |
| Exhibit 99.4 | Press release dated November 17, 2016: Sanofi and Regeneron Announce Praluent® (alirocumab) Cardiovascular Outcomes Trial will Continue as Planned Following Interim Analysis | |
2
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: November 18, 2016 | SANOFI | |||||
| By | /s/ Alexandra Roger | |||||
| Name: | Alexandra Roger | |||||
| Title: | Head of Securities Law and Capital Markets | |||||
3
| Exhibit No. |
Description | |
| Exhibit 99.1 | Press release dated October 28, 2016: Sanofi and Regeneron Receive Complete Response Letter from FDA for Sarilumab, an Investigational Treatment for Rheumatoid Arthritis | |
| Exhibit 99.2 | Press release dated November 11, 2016: Sanofi Receives CHMP Recommendation for Approval of SuliquaTM in the EU | |
| Exhibit 99.3 | Press release dated November 16, 2016: Sanofi and Regeneron Present Results from Phase 3 MONARCH Study of Investigational Sarilumab at American College of Rheumatology Annual Meeting | |
| Exhibit 99.4 | Press release dated November 17, 2016: Sanofi and Regeneron Announce Praluent® (alirocumab) Cardiovascular Outcomes Trial will Continue as Planned Following Interim Analysis | |
4
| This ‘6-K’ Filing | Date | Other Filings | ||
|---|---|---|---|---|
 | ||||
| Filed on / For Period End: | 11/18/16 | |||
| 11/17/16 | ||||
| 11/16/16 | ||||
| 11/11/16 | ||||
| 10/28/16 | 6-K | |||
| List all Filings | ||||