Delaware
|
001-36112
|
06-1591613
|
(State or Other Jurisdiction
of Incorporation)
|
(Commission
File Number) |
(IRS Employer
Identification No.) |
9640 Medical Center Drive,
Rockville, Maryland
|
20850
|
(Address of Principal Executive Offices)
|
(Zip Code)
|
Date: March 3, 2015
|
MACROGENICS, INC.
|
|
|
By:
|
/s/James Karrels
James Karrels
Chief Financial Officer
|
·
|
Phase 3 Metastatic Breast Cancer Study: The Company expects to commence SOPHIA, a Phase 3 pivotal study in approximately 530 subjects, in the third quarter of 2015. This study is planned to evaluate margetuximab plus chemotherapy against trastuzumab plus chemotherapy in third-line metastatic breast cancer patients with HER2 expression at the 3+ level by immunohistochemistry (IHC) or 2+ level by IHC with gene amplification, subject to completion of further regulatory review. MacroGenics projects that it will take approximately three years to complete this study, which will include an interim futility analysis.
|
·
|
Presentation of Phase 1 Data: In mid-2015, MacroGenics plans to present margetuximab Phase 1 clinical data for patients with breast cancer in expansion cohorts testing once-every-three-week dosing regimens.
|
·
|
Recruiting Additional Monotherapy Expansion Cohorts: During the fourth quarter of 2014, the Company initiated recruitment of patients in multiple additional monotherapy expansion cohorts across various tumor types, including triple-negative breast cancer, head and neck cancer, renal cell cancer, melanoma (in patients who have failed a checkpoint inhibitor), and a cohort consisting of non-small cell lung cancer and bladder cancer patients with the highest level of B7-H3 expression.
|
·
|
Presentation of Phase 1 MGA271 Data: In the second half of 2015, MacroGenics plans to present Phase 1 clinical data for MGA271.
|
·
|
Combination Studies: MacroGenics plans to initiate studies of MGA271 in combination with other immuno-oncology agents in 2015, including a combination study with ipilimumab in B7-H3 positive melanoma, lung, and head and neck cancers.
|
·
|
MGD010 Nearing Phase 1 Clinical Initiation: MGD010 is a DART molecule for the treatment of autoimmune disorders that simultaneously targets CD32B and CD79B, which are two B-cell surface proteins. MGD010 is designed to inhibit B-cell activation by exploiting the inhibitory function of CD32B, a checkpoint molecule expressed by B cells. MacroGenics expects to initiate a Phase 1a study in normal healthy volunteers in the first half of 2015. This product candidate is subject to a global collaboration with Takeda.
|
·
|
Introducing MGD009: In late 2015, MacroGenics anticipates initiating a Phase 1 clinical study of MGD009, a humanized DART molecule that recognizes both CD3 and an undisclosed antigen expressed on many solid tumor types. MacroGenics retains worldwide development and commercialization rights to this molecule.
|
·
|
Janssen Biotech, Inc.: In December 2014, MacroGenics entered into a global collaboration and license agreement with Janssen Biotech, Inc. for MGD011. Johnson & Johnson Innovation – JJDC, Inc. concurrently agreed to make an equity investment in MacroGenics. Upon closing of these agreements in 2015, MacroGenics received a total of $125 million. MGD011 is a humanized CD19 x CD3 bi-specific DART protein being developed for the treatment of B-cell hematological malignancies. Janssen will be fully responsible for developing MGD011 following submission of the IND, which is planned for 2015. MacroGenics may elect to fund a portion of late-stage clinical development in exchange for a profit share in the U.S. and Canada.
|
·
|
Takeda: In May 2014, MacroGenics announced that it had entered into an option agreement with Takeda Pharmaceutical Company Limited for the development and commercialization of MGD010. In September 2014, MacroGenics announced that it had entered into a second strategic alliance with Takeda. The second collaboration was for the development and commercialization of additional DART molecules.
|
·
|
Servier: In February 2014, MacroGenics announced that Servier had exercised its exclusive option to develop and commercialize MGD006. MacroGenics has retained exclusive development and commercial rights in the U.S., Canada, Mexico, Japan, South Korea and India. Servier has rights in all other countries.
|
·
|
Cash Position: Cash and cash equivalents as of December 31, 2014 were $157.6 million, compared to $116.5 million as of December 31, 2013. In the first quarter of 2015, MacroGenics closed a global collaboration and license agreement for MGD011 with Janssen Biotech, Inc. and received a $50 million upfront license fee, and Johnson & Johnson Innovation - JJDC, Inc. invested $75 million with the purchase of new shares of MacroGenics common stock at a price of $39.00 per share.
|
·
|
Revenue: Total revenues, consisting primarily of revenue from collaborative research, were $47.8 million for the year ended December 31, 2014, compared to $58.0 million for the year ended December 31, 2013. Collaborative research revenue includes the recognition of deferred revenue from payments received in previous periods as well as payments received during the year.
|
|
R&D Expenses: Research and development expenses were $70.2 million for the year ended December 31, 2014, compared to $46.6 million for the year ended December 31, 2013. This increase was primarily due to the initiation of clinical manufacturing activities for two product candidates and the advancement of the Company's clinical and pre-clinical programs.
|
|
G&A Expenses: General and administrative expenses were $15.9 million for the year ended December 31, 2014, compared to $11.1 million for the year ended December 31, 2013. This increase was primarily due to higher stock-based compensation expense as well as an increase in professional fees and other costs associated with public company operations.
|
·
|
Net Loss: Net loss was $38.3 million for the year ended December 31, 2014, compared to net loss of $0.3 million for the year ended December 31, 2013.
|
·
|
Shares Outstanding: Shares outstanding as of December 31, 2014 were 27,995,638 million. This excludes the 1,923,077 shares issued to Johnson & Johnson Innovation - JJDC, Inc., in January 2015.
|
·
|
Financial Guidance: MacroGenics expects that its current cash and cash equivalents, combined with anticipated funding under its strategic collaborations, should fund the Company's operations into 2018.
|
As of December 31,
|
||||||||
2014
|
2013
|
|||||||
Cash and cash equivalents
|
$
|
157,591
|
$
|
116,481
|
||||
Total assets
|
173,886
|
125,782
|
||||||
Deferred revenue
|
30,720
|
27,403
|
||||||
Total stockholders' equity
|
121,286
|
78,914
|
Year Ended December 31,
|
||||||||||||
2014
|
2013
|
2012
|
||||||||||
Revenues:
|
||||||||||||
Revenue from collaborative research
|
$
|
47,264
|
$
|
56,753
|
$
|
59,646
|
||||||
Grant revenue
|
533
|
1,282
|
4,180
|
|||||||||
Total revenues
|
47,797
|
58,035
|
63,826
|
|||||||||
Costs and expenses:
|
||||||||||||
Research and development
|
70,186
|
46,582
|
45,433
|
|||||||||
General and administrative
|
15,926
|
11,087
|
10,188
|
|||||||||
Total costs and expenses
|
86,112
|
57,669
|
55,621
|
|||||||||
Income (loss) from operations
|
(38,315
|
)
|
366
|
8,205
|
||||||||
Other income (expense)
|
2
|
(627
|
)
|
157
|
||||||||
Net comprehensive income (loss)
|
$
|
(38,313
|
)
|
$
|
(261
|
)
|
$
|
8,362
|
||||
Basic and diluted net income (loss) per common share
|
$
|
(1.40
|
)
|
$
|
(0.04
|
)
|
$
|
0.00
|
||||
Basic and diluted weighted average number of common shares
|
27,384,990
|
6,847,697
|
1,083,276
|