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 of
The
Securities Exchange Act of 1934
For
the month of January 2019
COMMISSION
FILE Number.
000-29338
CORREVIO
PHARMA CORP.
(Translation
of registrant’s name into English)
1441
Creekside Drive, 6th floor
Vancouver,
British Columbia, V6J 4S7, CANADA
(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
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): ☐
DOCUMENTS INCLUDED AS PART OF THIS REPORT
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.
| |
CORREVIO
PHARMA CORP. |
| |
(Registrant) |
| |
|
|
| Date: January 17, 2019 |
By: |
/s/
Justin Renz |
| |
|
Name: Justin Renz |
| |
|
Title: President and Chief Financial
Officer |
Exhibit 99.1
Correvio Provides Update On At The Market
Offering
NASDAQ: CORV TSX: CORV
VANCOUVER, Jan. 17, 2019 /CNW/ - Correvio
Pharma Corp. (NASDAQ: CORV) (TSX: CORV), a revenue-generating, specialty pharmaceutical company focused on commercializing hospital
drugs, today announced the completion of sales of all common shares qualified under its ATM Prospectus Supplement (defined below).
The Company's at-the-market sales issuance agreement, dated July 10, 2018, between the Company and B.Riley FBR, Inc., as agent,
continues in force. However, the Company has no present intention to file a new prospectus supplement to qualify the sale of additional
common shares pursuant to the sales agreement.
The common shares were sold by way of a prospectus
supplement (the "ATM Prospectus Supplement") to the Company's Canadian final base shelf prospectus and U.S. final base
shelf prospectus, filed under a registration statement on Form F-10, each dated July 5, 2018 (together, the "Base Shelf Prospectuses").
The approximately 4.3 million common shares were sold at an average price of US$2.71 per share, resulting in net proceeds to the
Company of approximately US$11.5 million. Based on its current operating plan, the Company expects that the net proceeds, combined
with its existing cash, provides it with sufficient capital to operate its business through the submission and U.S. Food and Drug
Administration review of the Brinavess® new drug application filing. Copies of the ATM prospectus supplements (together
with the related Base Shelf Prospectuses) may be obtained from Correvio by submitting a request to Correvio Investor Relations
at 1441 Creekside Drive, 6th Floor, Vancouver, BC Canada, V6J 4S7 or under the Company's profile on SEDAR at www.SEDAR.com or
on EDGAR at www.sec.gov.
This press release shall not constitute an
offer to sell or a solicitation of an offer to buy, nor shall there be any sale, of the Company's common shares in any jurisdiction
in which an offer solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any
such jurisdiction.
About Correvio Pharma Corp.
Correvio Pharma Corp. is a revenue-generating,
specialty pharmaceutical company focused on providing innovative, high-quality brands that meet the needs of acute care physicians
and patients. With a commercial presence and distribution network covering over 60 countries worldwide, Correvio develops, acquires
and commercializes brands for the in-hospital, acute care market segment. The Company's portfolio of approved and marketed brands
includes: Xydalba™ (dalbavancin hydrochloride), for the treatment of acute bacterial skin and skin structure infections
(ABSSSI); Zevtera®/Mabelio® (ceftobiprole medocaril sodium), a cephalosporin antibiotic for the treatment
of community- and hospital-acquired pneumonia (CAP, HAP); Brinavess® (vernakalant IV) for the rapid conversion of
recent onset atrial fibrillation to sinus rhythm; Aggrastat® (tirofiban hydrochloride) for the reduction of thrombotic
cardiovascular events in patients with acute coronary syndrome, and Esmocard® and Esmocard Lyo® (esmolol
hydrochloride), a short-acting betablocker used to control rapid heart rate in a number of cardiovascular indications. Correvio's
pipeline of product candidates includes Trevyent®, a drug device combination that is designed to deliver treprostinil,
the world's leading treatment for pulmonary arterial hypertension. Correvio is traded on the Nasdaq Capital Market (CORV) and the
Toronto Stock Exchange (CORV).
Forward-Looking Statement Disclaimer
Certain statements in this news release contain
forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995 or forward-looking information
under applicable Canadian securities legislation ("forward-looking statements") that may not be based on historical fact,
including without limitation statements containing the words "may", "continue", "expect" and similar
expressions. Forward-looking statements may involve, but are not limited to, statements regarding at-the-market offerings, including
the Company's intentions with respect to the filing of further prospectus supplements, the intended use of proceeds from the sales
of common shares under the ATM Prospectus Supplement, the sufficiency of capital under the Company's operating plan and the timing
of the U.S. Food and Drug Administration's determination with respect to the new drug application filing for Brinavess®
(vernakalant IV). Such forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause
the actual results, events or developments to be materially different from any future results, events or developments expressed
or implied by such forward-looking statements. All of the risks and certainties disclosed in these filings are hereby incorporated
by reference in their entirety. While Correvio makes these forward-looking statements in good faith, given these risks, uncertainties
and factors, you are cautioned not to place undue reliance on any forward-looking statements made in this press release. All forward-looking
statements made herein are based on our current expectations and we undertake no obligation to revise or update such forward-looking
statements to reflect subsequent events or circumstances, except as required by law.
Correvio® and the Correvio Logo
are the proprietary trademarks of Correvio Pharma Corp.
Aggrastat® and Brinavess® are trademarks owned by Correvio and its affiliates worldwide.
Xydalba™ is a trademark of Allergan Pharmaceuticals International Limited, and used under license.
Zevtera® and Mabelio® are trademarks owned by Basilea Pharmaceutica International Ltd., and used
under license.
Esmocard® and Esmocard Lyo® are trademarks owned by Orpha-Devel Handels und Vertriebs GmbH, and used
under license.
Trevyent® is a trademark of SteadyMed Ltd. and used under license.
All other trademarks are the property of their respective owners.
View
original content:http://www.prnewswire.com/news-releases/correvio-provides-update-on-at-the-market-offering-300780137.html
SOURCE Correvio Pharma Corp
View original content: http://www.newswire.ca/en/releases/archive/January2019/17/c1937.html
%CIK: 0001036141
For further information: Justin Renz, President and CFO, Correvio
Pharma Corp., 604.677.6905 ext. 128, 800.330.9928, jrenz@correvio.com; Argot Partners, Michelle Carroll/Claudia Styslinger, 212.600.1902,
michelle@argotpartners.com/claudia@argotpartners.com
CO: Correvio Pharma Corp
CNW 08:00e 17-JAN-19
This regulatory filing also includes additional resources:
ex991.pdf
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