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 April 2018
COMMISSION
FILE Number.
000-29338
CARDIOME
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.
|
CARDIOME
PHARMA CORP. |
|
(Registrant) |
|
|
|
Date: April 12, 2018 |
By: |
/s/
Justin Renz |
|
|
Name: Justin Renz |
|
|
Title: Chief Financial Officer |
Exhibit 99.1
Cardiome Announces Fifteen Xydalba™ and Zevtera®
Abstracts at ECCMID 2018
NASDAQ: CRME TSX: COM
Company Will Also Host Xydalba Expert
Educational Session Featuring Key Opinion Leaders in the Field of Hospital Anti-Infectives
VANCOUVER, April 12, 2018 /CNW/ - Cardiome Pharma Corp.
(NASDAQ:CRME / TSX:COM), a revenue-generating, specialty pharmaceutical company focused on commercializing hospital drugs, today
announced 15 data presentations taking place at the 28th European Congress of Clinical Microbiology and Infectious Disease
(ECCMID), being held April 21-24, 2018 in Madrid, Spain. The presentations will include data for the Company's commercial
anti-infective assets, Xydalba™ (dalbavancin hydrochloride) and Zevtera/Mabelio (ceftobiprole), an intravenous (IV) cephalosporin
antibiotic with rapid bactericidal activity against a wide range of Gram-positive and Gram-negative bacteria, including methicillin-resistant
Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa.
In addition to the data presentations at the meeting, Cardiome
will also be hosting an educational session featuring presentations by several physician experts regarding emerging anti-infective
treatments and clinical experience with Xydalba, the first and only 30-minute, one-dose treatment option for acute bacterial skin
and skin structure infections (ABSSSI). The details for the Xydalba symposium are as follows:
| · | Session title: Paradigm Shift in the Treatment
of Gram-positive Infections
Chairpersons: Christian Chidiac, Croix-Rousse Hospital,
Lyon, and Luis Eduardo Lopez-Cortes, University Hospital Virgen Macarena, Sevilla
Speakers: David Livermore, Norwich Medical School,
Norwich, Beatrice Grabein, University of Munich Grosshadern, Klaus Freidrich Bodmann, Werner Forßmann Hospital, Eberswalde,
Aurelien Dinh, HU Raymond Poincare APHP, Paris, Neil Ritchie, Queen Elizabeth University Hospital Glasgow, Glasgow
Date and time: Saturday, 21 April 2018 from 16:30
– 18:30 CEST
Onsite location: Hall K |
Cardiome currently markets Xydalba in France, Germany, the
UK, the Republic of Ireland, Netherlands, Finland and Sweden. The Company currently markets ceftobiprole under the brand
name Mabelio in Italy and France and under the brand name Zevtera in the UK, Germany, Austria and Switzerland, and will soon be
launching Zevtera in Spain.
The details for the data presentations at ECCMID are as
follows:
Xydalba presentations
Title: Reduced hospital stays for skin infections treated
with dalbavancin
Lead author: Robert Laing, Aberdeen, United Kingdom
Date and time: Saturday, 21 April 2018; 15:30 – 16:30 CEST
Location: Paper Poster Arena
Poster number: #P0282
Session info: PS018 – Clinical trial experience – new antibacterial agents
Title: Simulated dalbavancin exposures select for dalbavancin-nonsusceptible,
vancomycin-intermediate (VISA) strains of methicillin-resistant Staphylococcus aureus (MRSA) in in vitro pharmacokinetic/pharmacodynamic
models
Lead author: Brian Werth, Seattle, WA, USA
Date and time: Saturday, 21 April 2018; 15:30 – 16:30 CEST
Location: Paper Poster Arena
Poster number: #P0264
Session info: PS017 – Preclinical PK/PD
Title: Long-term outcomes of dalbavancin for the treatment
of osteomyelitis in adult patients
Date and time: Monday, 23 April 2018; 09:00 – 10:00 CEST
Lead author: Urania Rappo, Jersey City, NJ, USA
Location: ePoster Arena 3
ePoster number: #O0697 (mini oral session)
Session info: OE133 – Osteomyelitis: Optimal treatment options
Title: Can dalbavancin be used as a catheter lock solution?
Date and time: Monday, 23 April 2018; 12:30 – 13:30 CEST
Lead author: María Guembe, Madrid, Spain
Location: Paper Poster Arena
Poster number: #P1425
Session info: PS072 – Biofilms I – Gram-positive pathogens
Title: Dalbavancin as treatment for endocarditis and/or
bloodstream infections produced by Gram-positive cocci
Lead author: Carmen Hidalgo Tenorio, Granada, Spain
Date and time: Tuesday, 24 April 2018; 12:30 – 13:30 CEST
Location: Paper Poster Arena
Poster number: #P2017
Session info: PS099 – What is new in infective endocarditis?
Title: In vitro activity of dalbavancin against daptomycin-unsusceptible
and daptomycin-high-level-resistant MRSA and MSSA
Lead author: Juan-Luis Munoz-Bellido, Salamanca, Spain
Date and time: Tuesday, 24 April 2018; 12:30 – 13:30 CEST
Location: Paper Poster Arena
Poster number: #P2060
Session info: PS102 – MRSA: epidemiology and susceptibility
Title: In vitro antibacterial and bactericidal activity
of dalbavancin against different multidrug resistant (MDR) Staphylococcus aureus strains
Lead author: Floriana Campanile, Catania, Italy
Date and time: Tuesday, 24 April 2018; 12:30 – 13:30 CEST
Location: Paper Poster Arena
Poster number: #P2061
Session info: PS102 – MRSA: epidemiology and susceptibility
Title: In vitro activity of tedizolid, dalbavancin
and ceftobiprole against Clostridium difficile
Date and time: Monday, 23 April 2018; 13:30 – 14:30 CEST
Lead author: Avi Peretz, Teberias, Israel
Location: Paper Poster Arena
Poster number: #P1844
Session info: PS091 – Resistance in various Gram-positives
Zevtera Presentations
Title: Activity of ceftobiprole and comparators against
a collection of teicoplanin- and/or linezolid-resistant coagulase-negative staphylococci from bloodstream infections
Lead author: Marco Coppi, Florence, Italy
Date and time: Saturday, 21 April to Tuesday, 24 April 2018
Location: ePoster terminals
ePoster number: #E0003
Session info: EV001 – MRSA: Antibacterial susceptibility and resistance
Title: Activity of ceftobiprole and comparators against
European respiratory-tract isolates of MSSA and MRSA from 2016
Lead author: Ian Morrissey, Monthey, Switzerland
Date and time: Saturday, 21 April to Tuesday, 24 April 2018
Location: ePoster terminals
ePoster number: #E0006
Session info: EV001 – MRSA: Antibacterial susceptibility and resistance
Title: Ceftobiprole versus vancomycin in treatment
of methicillin-resistant Staphylococcus aureus (MRSA) meningitis in an experimental rabbit model
Lead author: Oguz, Resat Sipahi, Izmir, Turkey
Date and time: Saturday, 21 April 2018; 15:30 – 16:30 CEST
Location: Paper Poster Arena
Poster number: #P0263
Session info: PS017 – Preclinical PK/PD
Title: In vitro susceptibility testing of cerufoxime,
cefixime, cefpodoxime, cefotaxime, ceftaroline, ceftobiprole, linezolid and tedizolid against isolates of Nocardia by using the
E-test method
Lead author: Veronica Rodriguez-Nava, Lyon, France
Date and time: Monday, 23 April 2018; 13:30 – 14:30 CEST
Location: Paper Poster Arena
Poster number: #P1841
Session info: PS091 – Resistance in various Gram-positives
Title: In vivo assessment of ceftobiprole versus daptomycin
in a murine model of Staphylococcus aureus bacteremia: antimicrobial activity and impact on host inflammatory response
Lead author: Cédric Jaqueline, Nantes, France
Date and time: Tuesday, 24 April 2018; 12:30 – 13:30 CEST
Location: Paper Poster Arena
Poster number: #P2025
Session info: PS100 – News on staphylococcal bloodstream infection
Title: Epidemiology and ceftobiprole susceptibility
of European Enterobacteriaceae and Gram-positive clinical isolates from different infection sources collected in 2016
Lead author: Stephen Hawser, Monthey, Switzerland
Date and time: Tuesday, 24 April 2018; 12:30 – 13:30 CEST
Location: Paper Poster Arena
Poster number: #P2441
Session info: PS122 – Other (new) beta-lactams: In vitro activity against Gram-negatives
Title: Bactericidal and synergistic activity of ceftobiprole
combined with different antibiotics against selected Gram-positive isolates
Lead author: Floriana Campanile, Catania, Italy
Date and time: Tuesday, 24 April 2018; 12:30 – 13:30 CEST
Location: Paper Poster Arena
Poster number: #P2498
Session info: PS125 – Various aspects of antimicrobial susceptibility testing
About Xydalba™ (dalbavancin hydrochloride)
Xydalba™ (dalbavancin hydrochloride) for infusion is
a second generation, semi-synthetic lipoglycopeptide, which consists of a lipophilic side-chain added to an enhanced glycopeptide
backbone. Xydalba is the first and only 30-minute, one-dose treatment option for acute bacterial skin and skin structure infections
(ABSSSI) that delivers a full course of IV therapy. Xydalba can be administered as either one 1500 mg dose or as a two-dose regimen
of 1000 mg followed one week later by 500 mg, each administered over 30 minutes. Xydalba demonstrates bactericidal activity in
vitro against a range of Gram-positive bacteria, such as Staphylococcus aureus (including methicillin-resistant, also known as
MRSA, strains) and Streptococcus pyogenes, as well as certain other streptococcal species. Dalbavancin was approved by the
U.S. Food and Drug Administration in 2014 for the treatment of adult patients with ABSSSI caused by susceptible Gram-positive bacteria,
including methicillin resistant staphylococcus aureus (MRSA) and is commercialized under the trade name DALVANCE®.
Dalbavancin was also approved by the European Medicines Agency for the treatment of ABSSSIs in adults and is commercialized under
the tradename Xydalba. Xydalba is marketed by Cardiome in six countries, including the United Kingdom, France, Germany, Sweden,
Finland and the Republic of Ireland.
About Zevtera® / Mabelio®
(ceftobiprole)
Zevtera® (ceftobiprole medocaril sodium) is
a cephalosporin antibiotic for intravenous administration with rapid bactericidal activity against a wide range of Gram-positive
and Gram-negative bacteria, including methicillin-susceptible and resistant Staphylococcus aureus (MSSA, MRSA) and susceptible
Pseudomonas spp. Ceftobiprole is currently approved for sale in 13 European countries and several non-European countries
for the treatment of adult patients with community-acquired pneumonia (CAP) and hospital-acquired pneumonia (HAP), excluding ventilator-associated
pneumonia (VAP). Ceftobiprole is currently commercialized in Italy, France, Germany, the U.K., Austria and Switzerland under the
brand name Zevtera or Mabelio®.
About Cardiome Pharma Corp.
Cardiome 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, Cardiome 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 beta-blocker
used to control rapid heart rate in a number of cardiovascular indications. Cardiome's pipeline of product candidates includes
Trevyent®, a drug device combination that is designed to deliver Remodulin® (treprostinil) the world's leading
treatment for pulmonary arterial hypertension.
Cardiome is traded on the NASDAQ Capital Market (CRME) and
the Toronto Stock Exchange (COM). For more information, please visit our web site at www.cardiome.com.
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 "believe", "may", "plan", "will", "estimate",
"continue", "anticipate", "intend", "expect" and similar expressions. 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.
A discussion of the risks and uncertainties facing Cardiome are discussed in our most recent annual and quarterly reports and detailed
from time to time in our other filings with the Securities and Exchange Commission ("SEC") available at www.sec.gov and
the Canadian securities regulatory authorities at www.sedar.com. All of the risks and certainties disclosed in these filings
are hereby incorporated by reference in their entirety. While Cardiome 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.
Cardiome® and the Cardiome Logo are the proprietary
trademarks of Cardiome Pharma Corp.
Aggrastat® and Brinavess® are trademarks owned by Cardiome and its affiliates worldwide.
Xydalba™ is a trademark of Durata Therapeutics Holding C.V., 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 and used under license.
DALVANCE® is a trademark of Allergan Pharmaceuticals International Limited.
All other trademarks are the property of their respective owners.
View
original content:http://www.prnewswire.com/news-releases/cardiome-announces-fifteen-xydalba-and-zevtera-abstracts-at-eccmid-2018-300628714.html
SOURCE Cardiome Pharma Corp.
View original content: http://www.newswire.ca/en/releases/archive/April2018/12/c5808.html
%CIK: 0001036141
For further information: Justin Renz, CFO, Cardiome Pharma
Corp., 604.677.6905 ext. 128, 800.330.9928, jrenz@cardiome.com; Argot Partners, Michelle Carroll, 212.600.1902, michelle@argotpartners.com
CO: Cardiome Pharma Corp.
CNW 07:00e 12-APR-18
This regulatory filing also includes additional resources:
ex991.pdf
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