Ambrx Biopharma Inc. Reports 1H 2022 Financial Results and Provides Corporate Update
Ambrx Biopharma Inc. (NYSE: AMAM) appointed Kate Hermans as Interim CEO, succeeding Feng Tian. The company reported a revenue decline to $2.9 million for H1 2022, down from $5.1 million in H1 2021. R&D expenses rose to $32.8 million, primarily due to increased clinical trial costs. The net loss for the period was $51.5 million, compared to $29.0 million in the previous year. Ambrx received FDA clearance for ARX305 and included ARX788 in a key clinical trial, signaling ongoing commitment to its development pipeline amidst financial challenges.
- FDA granted 'Study May Proceed' letter for ARX305.
- ARX788 included in I-SPY 2.2 Phase 2 Clinical Trial.
- Appointment of experienced Interim CEO Kate Hermans.
- Revenue decreased to $2.9 million from $5.1 million year-over-year.
- Net loss increased to $51.5 million from $29.0 million year-over-year.
- R&D expenses rose significantly to $32.8 million.
- Appointed
"I am very grateful for all that Tian accomplished during his tenure leading
1H 2022 and Subsequent Highlights
-
Appointed
Kate Hermans as Interim Chief Executive Officer. In August,Ambrx announced the appointment ofKate Hermans as Interim Chief Executive Officer (CEO), replacingFeng Tian , Ph.D.Ms. Hermans has more than two decades of commercial and operational experience in the healthcare industry, previously serving in executive leadership roles at companies includingRadius Health , Bristol Myers Squibb and Pfizer. Ambrx’s Board has commenced a search for a permanent CEO.Dr. Tian has agreed to continue withAmbrx in an advisory capacity. -
Received a “Study May Proceed” letter from the FDA related to an IND application for ARX305. In February,
Ambrx announced that the FDA accepted the company’s IND and provided a “Study May Proceed” letter for ARX305 for the treatment of solid and hematological tumors. ARX305 is the third antibody drug conjugate (ADC) developed byAmbrx on its proprietary EPB platform to receive IND clearance. In July, Ambrx’s partner inChina , NovoCodex, announced that it had received drug clinical trial approval notice for ARX305 and intends to initiate a Phase 1 trial inChina in the second half of 2022. -
Announced Inclusion of ARX788 in a Quantum Leap’s I-SPY 2.2 Phase 2 Clinical Trial. In April, the company announced the inclusion of ARX788 in Quantum Leap Healthcare Collaborative’s investigational treatment arm in the I-SPY 2.2 TRIAL for the treatment of HER2-positive breast cancer in the neoadjuvant setting. Sponsored by Quantum Leap, I-SPY 2.2 is an adaptive Phase 2 clinical trial that evaluates emerging targeted agents, allowing those agents to either be combined with less toxic chemotherapeutic regimens or to replace cytotoxic chemotherapy entirely. The first patient was dosed with ARX788 in
August 2022 . -
Appointed
Janice Lu , M.D., Ph.D., as Chief Medical Officer. In May,Janice Lu , M.D., Ph.D., joinedAmbrx as its Chief Medical Officer.Dr. Lu is a distinguished clinical professor of medicine who has more than 18 years of experience in leading clinical trials and breast cancer drug development.Dr. Lu , a board-certified medical oncologist, was on the faculty in Hematology and Oncology atUCLA , and most recently served as Clinical Professor of Medicine and Medical Director of the Breast Oncology Program at theUSC Keck School of Medicine . -
Strengthened Board of Directors. In August,
Ambrx announced the appointment of Katrin Rupalla, Ph.D. to Chair of the Board of Directors. Since the start of 2022,Ambrx has appointedPaul V. Maier ,Janet Loesberg , Pharm. D.,Edward Hu andKate Hermans to its Board.
Financial Highlights
-
Cash and
Cash Equivalents and Marketable Securities : Cash and cash equivalents and marketable securities were as of$129.7 million June 30, 2022 , of which are marketable securities, compared to$64.1 million in cash and cash equivalents as of$170.1 million December 31, 2021 . -
Revenue: Revenue was
for the six months ended$2.9 million June 30, 2022 , as compared to for the six months ended$5.1 million June 30, 2021 . The decrease was primarily driven by less revenue recognized in connection with our R&D and license agreements, partially offset by increased third party reimbursable charges. -
Research and development (R&D) expenses: R&D expenses were
for the six months ended$32.8 million June 30, 2022 , as compared to for the six months ended$22.1 million June 30, 2021 . The increase was mainly due to increased costs related to our clinical trial programs, primarily driven by our lead product candidate ARX788, and related manufacturing costs, partially offset by lower stock-based compensation expense. -
Impairment loss on intangible assets: The loss of
for the six months ended$9.7 million June 30, 2022 was driven by the impairment of intangible assets related to assets that were in development with a collaboration partner. -
General and administrative (G&A) expenses: G&A expenses were
for the six months ended$9.4 million June 30, 2022 , as compared to for the six months ended$8.4 million June 30, 2021 . The increase was mainly attributable to professional services and fees in connection with operating as a public company including directors & officer insurance. -
Other expenses, net: Other expense, net, for the six months ended
June 30, 2022 were , as compared to$0.9 million for the six month ended$3.9 million June 20, 2021 . The current period expense is mainly related to fees and interest incurred related to a promissory note settlement and capital reduction related to Ambrx Shanghai. -
Net loss: Net loss for the six months ended
June 30, 2022 was , as compared to$51.5 million for the six months ended$29.0 million June 30, 2021 .
About
Forward-Looking Statements
This press release includes certain “forward-looking statements” intended to qualify for the “safe harbor” from liability established by the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements may be identified by the words “anticipate,” believe,” “estimate,” “expect,” “intend,” “plan,” “project,” “may,” “will,” “could,” “should,” “seek,” “potential” and similar expressions, and include, without limitation, express or implied statements regarding Ambrx’s beliefs and expectations regarding the advancement and potential benefits of its product candidates, clinical development and strategic plans, the results of the strategic review of the company’s pipeline, Ms. Hermans’ anticipated contributions and the timing of program updates and milestones related to its product candidates. Forward-looking statements are based on Ambrx’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, those risks and uncertainties associated with: the continuing impact of the COVID-19 pandemic and other public health-related risks and events on Ambrx’s business, operations, strategy, goals and anticipated milestones; Ambrx’s ability to execute on its strategy including with respect to the timing of its R&D efforts, initiation of clinical trials and other anticipated milestones; risks associated with development of novel therapeutics, including potential delays in clinical trials and regulatory submissions and the fact that future clinical trial results may not be consistent with preliminary results or results from prior preclinical studies or clinical trials; Ambrx’s ability to fund operations as anticipated; and the additional risks and uncertainties set forth more fully under the caption “Risk Factors” in Ambrx’s Annual Report on Form 20-F filed with the
Condensed Consolidated Statements of Operations and Comprehensive Loss (Unaudited; In thousands, except share and per share data) |
||||||||
For the Six Months Ended |
||||||||
2022 |
2021 |
|||||||
Revenues |
$ |
2,912 |
|
$ |
5,132 |
|
||
Operating expenses: |
||||||||
Research and development |
|
32,766 |
|
|
22,079 |
|
||
Impairment of intangible assets |
|
9,660 |
|
|
- |
|
||
General and administrative |
|
9,393 |
|
|
8,355 |
|
||
Total operating expenses |
|
51,819 |
|
|
30,434 |
|
||
Loss from operations |
|
(48,907 |
) |
|
(25,302 |
) |
||
Other expense, net: |
||||||||
Investment income, net |
|
223 |
|
|
- |
|
||
Interest expense, net |
|
(965 |
) |
|
- |
|
||
Other expense, net |
|
(124 |
) |
|
(13 |
) |
||
Change in fair value of redeemable noncontrolling interests |
|
- |
|
|
(3,903 |
) |
||
Total other expense, net |
|
(866 |
) |
|
(3,916 |
) |
||
Loss before provision for income taxes |
|
(49,773 |
) |
|
(29,218 |
) |
||
Provision for income taxes |
|
(1,716 |
) |
|
(1 |
) |
||
Net loss |
|
(51,489 |
) |
|
(29,219 |
) |
||
Less: net loss attributable to the redeemable noncontrolling interests |
|
- |
|
|
209 |
|
||
Net loss attributable to |
$ |
(51,489 |
) |
$ |
(29,010 |
) |
||
Net loss per share attributable to |
$ |
(0.19 |
) |
$ |
(1.63 |
) |
||
Weighted-average ordinary shares used to compute net loss per share attributable to ordinary shareholders basic and diluted |
270,142,269 |
|
17,748,713 |
|||||
Other comprehensive loss, net of tax: |
||||||||
Net loss |
$ |
(51,489 |
) |
$ |
(29,219 |
) |
||
Foreign currency translation adjustment |
|
- |
|
|
(18 |
) |
||
Comprehensive loss |
|
(51,489 |
) |
|
(29,237 |
) |
||
Add: Unrealized loss on marketable debt securities, available-for-sale |
|
(217 |
) |
|
- |
|
||
Less: Comprehensive loss attributable to the redeemable noncontrolling interests |
|
- |
|
|
208 |
|
||
Comprehensive loss attributable to |
$ |
(51,706 |
) |
$ |
(29,029 |
) |
Condensed Consolidated Balance Sheets (Unaudited; In thousands, except share data) |
||||||||
|
|
|||||||
2022 |
2021 |
|||||||
Assets |
||||||||
Current assets: |
||||||||
Cash and cash equivalents |
$ |
65,642 |
|
$ |
170,064 |
|
||
Restricted cash |
|
831 |
|
|
842 |
|
||
Marketable debt securities, available-for-sale |
|
45,251 |
|
|
- |
|
||
Accounts receivable, net |
|
1,466 |
|
|
1,239 |
|
||
Prepaid expenses and other current assets |
|
7,816 |
|
|
4,661 |
|
||
Total current assets |
|
121,006 |
|
|
176,806 |
|
||
Marketable debt securities, available-for-sale, net of current portion |
|
18,827 |
|
|
- |
|
||
Property and equipment, net |
|
3,146 |
|
|
2,984 |
|
||
Right-of-use assets, net |
|
11,860 |
|
|
12,737 |
|
||
Intangible assets, net |
|
25,565 |
|
|
35,962 |
|
||
Other long-term assets |
|
466 |
|
|
530 |
|
||
Total assets |
$ |
180,870 |
|
$ |
229,019 |
|
||
Liabilities and Shareholders' Equity |
||||||||
Current liabilities: |
||||||||
Accounts payable |
$ |
5,696 |
|
$ |
5,272 |
|
||
Accrued liabilities |
|
15,585 |
|
|
14,125 |
|
||
Operating lease liabilities, current portion |
|
1,320 |
|
|
915 |
|
||
Deferred revenue, current portion |
|
3,137 |
|
|
4,267 |
|
||
Total current liabilities |
|
25,738 |
|
|
24,579 |
|
||
Operating lease liabilities, net of current portion |
|
11,251 |
|
|
12,212 |
|
||
Deferred tax liabilities |
|
880 |
|
|
880 |
|
||
Deferred revenue, net of current portion |
|
1,109 |
|
|
1,381 |
|
||
Total liabilities |
|
38,978 |
|
|
39,052 |
|
||
Shareholders' Equity: |
||||||||
Ordinary Shares, par value |
|
27 |
|
|
27 |
|
||
Additional paid-in capital |
|
407,993 |
|
|
404,362 |
|
||
Accumulated other comprehensive loss |
|
(1,007 |
) |
|
(790 |
) |
||
Accumulated deficit |
|
(265,121 |
) |
|
(213,632 |
) |
||
Total shareholders' equity |
|
141,892 |
|
|
189,967 |
|
||
Total liabilities and shareholders' equity |
$ |
180,870 |
|
$ |
229,019 |
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INVESTORS
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619-916-7620
ir@ambrx.com
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