Gamida Cell Reports Second Quarter 2019 Financial Results and Provides Company Update
– Successfully completed follow-on public offering raising approximately
– Patient enrollment in Phase 3 study of omidubicelexpected to be completed by year-end 2019; Topline data expected in first half of 2020 –
– Phase 1 clinical study of GDA-201 continues to progress, with additional data expected in the second half of 2019 –
“During the past quarter,
“Our second cell therapy program, GDA-201, is also moving forward. We anticipate additional data from the ongoing Phase 1/2 clinical study in the second half of the year. We are also on track with our plans to develop a cryopreserved formulation of GDA-201 to enable a multi-center clinical study in patients with non-Hodgkin lymphoma,” Dr. Adams continued. “Both omidubicel and GDA-201 are based on our proprietary cell expansion platform, which has the potential to further expand our pipeline. In June, we appointed Dr.
Program Highlights
- Continued to advance the Phase 3 clinical study of omidubicel: Patient enrollment continued to progress in the Gamida Cell’s Phase 3 study of omidubicel in patients with high-risk hematologic malignancies. The international, randomized, multi-center study is designed to evaluate the safety and efficacy of omidubicel compared to standard umbilical cord blood for allogeneic bone marrow transplant in approximately 120 patients with no available matched donor. The company anticipates completing patient enrollment by the end of this year with topline data anticipated in first half of 2020.
- Established agreements to support commercial manufacturing for omidubicel: In June,
Gamida Cell andLonza announced that the companies entered into a strategic manufacturing agreementfor the future commercial production after potentialFDA approval of omidubicel. This agreement follows a successful multi-year clinical manufacturing relationship and providesGamida Cell with a path to commercial supply of omidubicel. Under this multi-year agreement,Lonza will construct and dedicate production suites at itsGeleen, NL site for the anticipated commercial launch. Additionally, the agreement enablesGamida Cell to increase the number of dedicated production suites over time to ensure commercial supply.Gamida Cell also has the option of expanding further intoLonza's global cell and gene therapy manufacturing network. In August,Gamida Cell signed an agreement with Biopharmax for the construction of suites for the commercial manufacture of omidubicel after potentialFDA approval of omidubicel at aGamida Cell -operated facility inIsrael .
- Initiated enrollment for Cohort 2 in the Phase 1/2 study of omidubicel in patients with severe aplastic anemia: In June, patient enrollment began in Cohort 2 of the investigator-sponsored, Phase 1/2 clinical study of omidubicel in patients with severe aplastic anemia, a rare and life-threatening blood disorder. Earlier this year, encouraging data from Cohort 1 were reported at the 2019 Transplantation & Cellular Therapy (TCT) Meeting. All three patients enrolled in Cohort 1 successfully underwent a bone marrow transplant consisting of omidubicel plus a haploidentical stem cell graft. The rapid engraftment, sustained hematopoiesis and accelerated immune recovery observed in these patients enabled the initiation of Cohort 2, where patients will be treated with omidubicel as a stand-alone graft.
- Demonstrated continued progress with GDA-201 clinical development program:
Gamida Cell continued to make progress with the GDA-201 clinical development program. The investigator-sponsored, Phase 1/2 clinical study of GDA-201 in patient with non-Hodgkin lymphoma and multiple myeloma is ongoing, with additional data expected in the second half of 2019. The company is developing a cryopreserved formulation of GDA-201 to enable a multi-center, multi-dose Phase 1/2 clinical study in patients with non-Hodgkin lymphoma, which is expected to begin next year.
Corporate Highlights
- Completed public follow-on offering of approximately
$40 million in gross proceeds: In July,Gamida Cell announced that the company closed an underwritten public offering of 7,000,000 ordinary shares and that the underwriters exercised in full their option to purchase an additional 1,050,000 ordinary shares at the public offering price of$5.00 per share. The aggregate gross proceeds toGamida Cell from the offering, including the shares sold pursuant to the underwriters’ option, before deducting underwriting discounts and commission and offering expenses, were$40.3 million .
- Bolstered management team with appointment of
Tracey Lodie , Ph.D., as chief scientific officer: In June, the company announced the appointment ofTracey Lodie , Ph.D., as chief scientific officer. Prior to joiningGamida Cell , Dr. Lodie served as senior vice president, translational immunology at BlueRock Therapeutics, where she helped to advance their universal pluripotent stem cell platform into central nervous system, cardiovascular, and autoimmune therapeutic areas. She also served as vice president of immunology atSyros Pharmaceuticals , where she developed new autoimmunity and immuno-oncology research programs. Prior toSyros Pharmaceuticals , Dr. Lodie spent over 14 years at Sanofi-Genzyme, where she held roles of increasing responsibility. She obtained a PhD. in immunology and pathology atBoston University School of Medicine before completing a post-doctoral fellowship atBeth Israel Deaconess Medical Center in theDepartment of Hematology/Oncology .
Shawn Cline Tomasello andStephen Wills elected to Board of Directors, reflecting company’s progress toward commercialization: In June,Shawn Cline Tomasello andStephen T. Wills were elected to Gamida Cell’s board of directors. Ms. Tomasello has extensive experience in commercializing first-in-class medicines for the treatment of cancer, including Yescarta® (at Kite Pharma, now part ofGilead Sciences ) and Imbruvica® (at Pharmacyclics, now part ofAbbVie ). Mr. Wills has extensive operational, financial and transactional experience over nearly three decades in the life sciences and accounting industries. He has served as chief financial officer ofPalatin Technologies , a publicly-traded biotechnology company developing peptide therapeutics, since 1997 and also serves as Palatin’s chief operating officer and executive vice president.
Anticipated 2019-2020 Milestones
Gamida Cell’s anticipated program milestones in 2019-2020 are as follows:
Omidubicel
- Complete enrollment in Phase 3 study of omidubicel in patients with hematologic malignancies by the end of 2019
- Report topline data from the Phase 3 study of omidubicel in patients with hematologic malignancies in the first half of 2020
- Complete BLA submission for omidubicel in hematologic malignancies in the second half of 2020, should Phase 3 data be positive
GDA-201
- Complete patient enrollment in the ongoing Phase 1 study in the second half of 2019
- Present additional data at a medical meeting in the second half of 2019
-
Initiate multi-center, Phase 1/2 clinical study in patients with
NHL in 2020
Second Quarter 2019 Financial Results
-
Research and development (R&D) expenses in the second quarter of 2019 were
$7.0 million and were also$7.0 million in the same period in 2018. R&D expenses were higher in the second quarter of 2019 compared to the same period in 2018 due to the advancement of omidubicel and GDA-201 but were offset by a$2.0 million increase in grants related to theIsraeli Innovation Authority (IIA).
-
General and administrative expenses were
$3.8 million for the second quarter of 2019, compared to$2.9 million in the same period in 2018. The difference was attributable mainly to a$0.4 million increase in cash and non-cash expenses related to hiring and establishing the U.S. headquarters as well as a$0.5 million increase in professional services, including an increase in expenses associated with being a publicly-traded company.
-
Finance income, net, was
$16.8 million for the second quarter of 2019, compared to finance expenses, net, of$3.2 million in the same period in 2018. The net increase was primarily due to non-cash income resulting from the re-valuation of warrants, offset by non-cash expenses from the re-valuation of the IIA royalty-bearing grant liability.
-
Net income for the second quarter of 2019 was
$6.0 million , compared to a net loss of$13.1 million in the same period in 2018.
As of
2019 Financial Guidance
Conference Call Information
About Omidubicel
Omidubicel (formerly known as NiCord®), the company’s lead clinical program, is an advanced cell therapy under development as a potential life-saving allogeneic hematopoietic stem cell (bone marrow) transplant solution for patients with hematologic malignancies (blood cancers). Omidubicel is the first bone marrow transplant product to receive Breakthrough Therapy Designation from the
About GDA-201
Omidubicel and GDA-201 are investigational therapies, and their safety and efficacy have not been evaluated by the
About
Cautionary Note Regarding Forward Looking Statements
This press release contains forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995, including with respect to the patient enrollment in and timing of initiation and progress of and data reported from the clinical trials of Gamida Cell’s product candidates, and Gamida Cell’s expectations regarding its projected operating expenses and cash runway, which statements are subject to a number of risks, uncertainties and assumptions, including, but not limited to the scope, progress and expansion of Gamida Cell’s clinical trials and variability, and ramifications for the cost thereof; and clinical, scientific, regulatory and technical developments. In light of these risks and uncertainties, and other risks and uncertainties that are described in the Risk Factors section of Gamida Cell’s public filing on Form 20-F, filed with the
1Horwitz M.E., Wease S., Blackwell B., Valcarcel D. et al. Phase I/II study of stem-cell transplantation using a single cord blood unit expanded ex vivo with nicotinamide. J Clin Oncol. 2019 Feb 10;37(5):367-374.
2ClinicalTrials.gov identifier NCT02730299.
3ClinicalTrials.gov identifier NCT03173937.
4ClinicalTrials.gov identifier NCT03019666.
INTERIM CONSOLIDATED STATEMENTS OF FINANCIAL POSITION |
|||||||||
U.S. dollars in thousands |
|||||||||
|
|
June 30, |
|
December 31, |
|||||
|
|
2019 |
|
2018 |
|
2018 |
|||
|
|
Unaudited |
|
Audited |
|||||
ASSETS |
|
|
|
|
|
|
|||
|
|
|
|
|
|
|
|||
CURRENT ASSETS: |
|
|
|
|
|
|
|||
Cash and cash equivalents |
|
$ |
37,078 |
|
$ |
19,004 |
|
$ |
40,272 |
Available-for-sale financial assets |
|
|
4,618 |
|
|
9,632 |
|
|
20,417 |
Prepaid expenses and other current assets |
|
|
886 |
|
|
1,525 |
|
|
1,502 |
|
|
|
|
|
|
|
|||
Total current assets |
|
|
42,582 |
|
|
30,161 |
|
|
62,191 |
|
|
|
|
|
|
|
|||
NON-CURRENT ASSETS: |
|
|
|
|
|
|
|||
Property and equipment, net |
|
|
3,437 |
|
|
1,546 |
|
|
2,311 |
Right-of-use assets |
|
|
6,157 |
|
|
- |
|
|
- |
Other assets |
|
|
1,355 |
|
|
1,141 |
|
|
662 |
|
|
|
|
|
|
|
|||
Total non-current assets |
|
|
10,949 |
|
|
2,687 |
|
|
2,973 |
|
|
|
|
|
|
|
|||
Total assets |
|
$ |
53,531 |
|
$ |
32,848 |
|
$ |
65,164 |
LIABILITIES AND EQUITY |
|
|
|
|
|
|
|||
|
|
|
|
|
|
|
|||
CURRENT LIABILITIES: |
|
|
|
|
|
|
|||
Trade payables |
|
$ |
2,121 |
|
$ |
1,158 |
|
$ |
1,985 |
Employees and payroll accruals |
|
|
2,753 |
|
|
- |
|
|
2,888 |
Current maturities of lease liabilities |
|
|
1,945 |
|
|
- |
|
|
- |
Accrued expenses and other payables |
|
|
2,699 |
|
|
4,057 |
|
|
1,832 |
|
|
|
|
|
|
|
|||
Total current liabilities |
|
|
9,518 |
|
|
5,215 |
|
|
6,705 |
|
|
|
|
|
|
|
|||
NON-CURRENT LIABILITIES: |
|
|
|
|
|
|
|||
Liabilities presented at fair value |
|
|
7,654 |
|
|
13,700 |
|
|
24,049 |
Employee benefit liabilities, net |
|
|
274 |
|
|
217 |
|
|
183 |
Lease liability |
|
|
4,627 |
|
|
- |
|
|
- |
Liability to Israel Innovation Authority (IIA) |
|
|
10,906 |
|
|
9,753 |
|
|
9,540 |
|
|
|
|
|
|
|
|||
Total non-current liabilities |
|
|
23,461 |
|
|
23,670 |
|
|
33,772 |
|
|
|
|
|
|
|
|||
SHAREHOLDERS' EQUITY: |
|
|
|
|
|
|
|||
|
|
|
|
|
|
|
|||
Total shareholders' equity |
|
|
20,552 |
|
|
3,963 |
|
|
24,687 |
|
|
|
|
|
|
|
|||
Total liabilities and shareholders' equity |
|
$ |
53,531 |
|
$ |
32,848 |
|
$ |
65,164 |
INTERIMCONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME |
||||||||||||||||||||||
U.S. dollars in thousands(except share and per share data) |
||||||||||||||||||||||
|
|
Six months ended
|
|
Three months ended
|
Year ended
|
|||||||||||||||||
|
|
2019 |
|
2018 |
|
2019 |
|
2018 |
2018 |
|||||||||||||
|
|
Unaudited |
Audited |
|||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
||||||||||||
Research and development, net |
|
$ |
14,319 |
|
|
$ |
12,037 |
|
|
$ |
7,036 |
|
|
$ |
6,977 |
|
|
$ |
22,045 |
|
||
General and administrative |
|
|
7,574 |
|
|
|
4,570 |
|
|
|
3,761 |
|
|
|
2,917 |
|
|
|
11,599 |
|
||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Operating loss |
|
|
21,893 |
|
|
|
16,607 |
|
|
|
10,797 |
|
|
|
9,894 |
|
|
|
33,644 |
|
||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Finance expenses |
|
|
1,604 |
|
|
|
4,204 |
|
|
|
1,336 |
|
|
|
3,230 |
|
|
|
20,259 |
|
||
Finance income |
|
|
(14,052 |
) |
|
|
(330 |
) |
|
|
(18,169 |
) |
|
|
(34 |
) |
|
|
(1,042 |
) |
||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Loss (income) before taxes on income |
|
|
9,445 |
|
|
|
20,481 |
|
|
|
(6,036 |
) |
|
|
13,090 |
|
|
|
52,861 |
|
||
Taxes on income |
|
|
100 |
|
|
|
- |
|
|
|
74 |
|
|
|
- |
|
|
|
70 |
|
||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Net loss (income) |
|
|
9,545 |
|
|
|
20,481 |
|
|
|
(5,962 |
) |
|
|
13,090 |
|
|
|
52,931 |
|
||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Net loss (income) per share: |
|
|
|
|
||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Basic net loss (income) per share |
|
$ |
0.38 |
|
|
$ |
29.69 |
|
|
$ |
(0.23 |
) |
|
$ |
18.97 |
|
|
$ |
10.53 |
|
||
|
|
|
|
|
|
|
|
|
|
|
||||||||||||
Diluted net loss (income) per share |
|
$ |
0.87 |
|
|
$ |
29.69 |
|
|
$ |
0.44 |
|
|
$ |
18.97 |
|
|
$ |
10.53 |
|
||
INTERIMCONSOLIDATED STATEMENTS OF CASH FLOWS |
||||||||||||||||||||
U.S. dollars in thousands |
||||||||||||||||||||
|
|
Six months ended
|
|
Three months ended
|
|
Year ended
|
||||||||||||||
|
|
2019 |
|
2018 |
|
2019 |
|
2018 |
|
2018 |
||||||||||
|
|
Unaudited |
|
Audited |
||||||||||||||||
Cash flows from operating activities: |
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Net (loss) income |
|
$ |
(9,545 |
) |
|
$ |
(20,481 |
) |
|
$ |
5,962 |
|
|
$ |
(13,090 |
) |
|
$ |
(52,931 |
) |
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Adjustments to reconcile net loss to net cash used in operating activities: |
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Adjustments to the profit or loss items: |
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Depreciation of property, plant and equipment and right-of-use assets |
|
|
1,245 |
|
|
|
97 |
|
|
|
703 |
|
|
|
48 |
|
|
|
269 |
|
Financial income, net |
|
|
(569 |
) |
|
|
(375 |
) |
|
|
(378 |
) |
|
|
(362 |
) |
|
|
(858 |
) |
Cost of share-based compensation |
|
|
2,410 |
|
|
|
1,623 |
|
|
|
1,319 |
|
|
|
779 |
|
|
|
3,575 |
|
Change in employee benefit liabilities, net |
|
|
8 |
|
|
|
17 |
|
|
|
(3 |
) |
|
|
33 |
|
|
|
(15 |
) |
Amortization of premium on available-for-sale financial assets |
|
|
101 |
|
|
|
(9 |
) |
|
|
51 |
|
|
|
(90 |
) |
|
|
272 |
|
Revaluation of financial derivatives |
|
|
(13,471 |
) |
|
|
3,400 |
|
|
|
(17,378 |
) |
|
|
3,000 |
|
|
|
17,600 |
|
Revaluation of liability to IIA |
|
|
1,199 |
|
|
|
2,600 |
|
|
|
631 |
|
|
|
2,188 |
|
|
|
2,037 |
|
|
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
(9,077 |
) |
|
|
7,353 |
|
|
|
(15,055 |
) |
|
|
5,596 |
|
|
|
22,880 |
|
Changes in asset and liability items: |
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Decrease (Increase) in prepaid expenses and other current assets and other assets |
|
|
117 |
|
|
|
(1,156 |
) |
|
|
(292 |
) |
|
|
(1,256 |
) |
|
|
942 |
|
Increase (decrease) in trade payables |
|
|
244 |
|
|
|
(1,232 |
) |
|
|
1,088 |
|
|
|
306 |
|
|
|
(405 |
) |
Increase in accrued expenses and other payables and employee and payroll accrual |
|
|
162 |
|
|
|
1,871 |
|
|
|
141 |
|
|
|
1,611 |
|
|
|
2,296 |
|
|
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
523 |
|
|
|
(517 |
) |
|
|
937 |
|
|
|
661 |
|
|
|
2,833 |
|
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Cash received during the period for: |
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Interest received |
|
|
830 |
|
|
|
391 |
|
|
|
309 |
|
|
|
378 |
|
|
|
792 |
|
Interest paid |
|
|
(51 |
) |
|
|
- |
|
|
|
(23 |
) |
|
|
- |
|
|
|
- |
|
|
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
779 |
|
|
|
391 |
|
|
|
286 |
|
|
|
378 |
|
|
|
792 |
|
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Net cash used in operating activities |
|
|
(17,320 |
) |
|
|
(13,254 |
) |
|
|
(7,870 |
) |
|
|
(6,455 |
) |
|
|
(26,426 |
) |
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Cash flows from investing activities: |
|
|
|
|
|
|
|
|
|
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Purchase of property and equipment |
|
|
(878 |
) |
|
|
(703 |
) |
|
|
(528 |
) |
|
|
(472 |
) |
|
|
(1,645 |
) |
Purchase of available-for-sale financial assets |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
(10,905 |
) |
Proceed from sale of available-for-sale financial assets |
|
|
- |
|
|
|
4,984 |
|
|
|
- |
|
|
|
- |
|
|
|
4,949 |
|
Proceed from maturity of available-for-sale financial assets |
|
|
15,740 |
|
|
|
- |
|
|
|
1,847 |
|
|
|
- |
|
|
|
- |
|
Proceeds from bank deposits |
|
|
- |
|
|
|
5,000 |
|
|
|
- |
|
|
|
- |
|
|
|
5,000 |
|
Investment in restricted bank deposits |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
(150 |
) |
|
|
|
|
|
|
|
|
|
|
|
||||||||||
Net cash provided by (used in) investing activities |
|
|
14,862 |
|
|
|
9,281 |
|
|
|
1,319 |
|
|
|
(472 |
) |
|
|
(2,751 |
) |
INTERIMCONSOLIDATED STATEMENTS OF CASH FLOWS |
|||||||||||||||||||
U.S. dollars in thousands |
|||||||||||||||||||
|
|
Six months ended
|
|
Three months ended
|
|
Year ended
|
|||||||||||||
|
|
2019 |
|
2018 |
|
2019 |
|
2018 |
|
2018 |
|||||||||
|
|
Unaudited |
|
Audited |
|||||||||||||||
Cash flows from financing activities: |
|
|
|
|
|
|
|
|
|
|
|||||||||
|
|
|
|
|
|
|
|
|
|
|
|||||||||
Receipt of grants from the IIA |
|
|
167 |
|
|
|
1,653 |
|
|
|
167 |
|
|
|
- |
|
|
|
612 |
Proceeds from issuance of shares, net |
|
|
(346 |
) |
|
|
- |
|
|
|
(108 |
) |
|
|
- |
|
|
|
47,479 |
Payment of lease liabilities |
|
|
(764 |
) |
|
|
- |
|
|
|
(324 |
) |
|
|
- |
|
|
|
- |
Exercise of options |
|
|
117 |
|
|
|
- |
|
|
|
117 |
|
|
|
- |
|
|
|
2 |
|
|
|
|
|
|
|
|
|
|
|
|||||||||
Net cash provided by (used in) financing activities |
|
|
(826 |
) |
|
|
1,653 |
|
|
|
(148 |
) |
|
|
- |
|
|
|
48,093 |
|
|
|
|
|
|
|
|
|
|
|
|||||||||
Exchange differences on balances of cash and cash equivalents |
|
|
90 |
|
|
|
- |
|
|
|
28 |
|
|
|
- |
|
|
|
31 |
|
|
|
|
|
|
|
|
|
|
|
|||||||||
Increase (decrease) in cash and cash equivalents |
|
|
(3,194 |
) |
|
|
(2,321 |
) |
|
|
(6,671 |
) |
|
|
(6,927 |
) |
|
|
18,947 |
Cash and cash equivalents at beginning of period |
|
|
40,272 |
|
|
|
21,325 |
|
|
|
43,749 |
|
|
|
25,931 |
|
|
|
21,325 |
|
|
|
|
|
|
|
|
|
|
|
|||||||||
Cash and cash equivalents at end of period |
|
$ |
37,078 |
|
|
$ |
19,004 |
|
|
$ |
37,078 |
|
|
$ |
19,004 |
|
|
$ |
40,272 |
|
|
|
|
|
|
|
|
|
|
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20190806005111/en/
Source:
Jaren Irene Madden
jaren@gamida-cell.com
617-892-9084
Krystle Gibbs (media)
krystle@tenbridgecommunications.com
508-479-6358