Compass Therapeutics Reports Fourth Quarter and Full Year 2021 Financial Results and Provides Corporate Update
Compass Therapeutics reported a strong financial position with $144.5 million in cash as of 2021, bolstered by a $136 million public offering. The company is advancing its clinical pipeline, particularly the CTX-009 study for advanced biliary tract cancers, which met response criteria for progression to Phase 2. Additionally, CTX-471 showed encouraging results in patients with solid tumors. However, the company faced a net loss of $82.2 million for 2021, with R&D expenses rising significantly to $20.3 million, marking a 36% increase from 2020. The company expects to sustain operations into late 2024.
- Strong cash position of $144.5 million at year-end 2021.
- Successful $136 million public offering to support pipeline development.
- CTX-009 met criteria to advance to Phase 2 in biliary tract cancers, showing 29% ORR.
- Encouraging results from CTX-471, with three partial responses reported.
- Net loss increased to $82.2 million in 2021, up from $29.5 million in 2020.
- R&D expenses rose 36% to $20.3 million, primarily due to a $6 million milestone payment.
- Ended 2021 with
$144.5 million in cash and cash equivalents - CTX-009 (DLL4 X VEGF-A bispecific antibody) Global Phase 2 study in patients with advanced biliary tract cancers (BTC) is progressing well; the response criteria required to advance the study to its second stage have been met (ORR =
29% for the first 17 evaluable patients) - The Company plans to update the results from the first stage of the BTC study in Q2 of 2022
- The FDA cleared the CTX-009 IND in January; US sites are expected to start opening in Q2 of 2022 and to begin dosing patients in Q3 of 2022
- CTX-471 (CD137 agonist): three partial responses were seen in the monotherapy study of patients with solid tumors who have previously progressed on PD-1 or PD-L1 therapy
BOSTON, March 21, 2022 (GLOBE NEWSWIRE) -- Compass Therapeutics, Inc. (Nasdaq: CMPX), a clinical-stage, oncology-focused biopharmaceutical company developing proprietary antibody-based therapeutics to treat multiple human diseases, today reported fourth quarter and full year 2021 financial results and provided a corporate update.
“In 2021 we strengthened our pipeline of innovative antibody-based therapeutics with the addition of CTX-009, a novel bispecific antibody targeting DLL4 and VEGF-A, two important signaling molecules in the angiogenesis pathways. We are excited to see the activity of CTX-009 across multiple solid tumors and happy to report that the criteria to advance our Global Phase 2 study to its second stage have already been met,” said Thomas J. Schuetz, MD, PhD, Co-Founder and Chief Executive Officer.
“Following our
Development Pipeline Update and Highlights:
CTX-009 a novel DLL4 x VEGF-A bispecific antibody:
- Completed a Phase 1a dose escalation and dose expansion study in 45 patients. CTX-009 demonstrated single agent activity in heavily pre-treated patients with solid tumors who progressed after prior anti-VEGF therapies. The maximum tolerated dose was not reached and CTX-009 was found to be generally well-tolerated.
- Completed a Phase 1b study of CTX-009 in combination with chemotherapy. This study demonstrated compelling activity of CTX-009 with chemotherapy in patients with biliary tract cancers and prompted the initiation of the first CTX-009 Phase 2 study.
- Enrolled and dosed 24 patients in the first stage of the CTX-009 Phase 2 study in biliary tract cancers. There were five confirmed partial responses among the first 17 evaluable patients, and all patients have reached stable disease or better, resulting in a
100% clinical benefit rate. The criteria to advance the study to its second stage have been met. - Filed an IND in the US and received clearance from the FDA to initiate a global Phase 2 study in the US and in South Korea. Importantly, all patients currently enrolled in the South Korea sites are included in this global study.
CTX-471, a monoclonal antibody agonist of CD137, a key co-stimulatory receptor on immune cells:
- Advanced a Phase 1b dose expansion study and enrolled 49 patients in the study as of February 25, 2022.
- Of the 38 evaluable patients, three patients had a partial response and 19 patients have reached stable disease.
CTX-8371 a bispecific antibody that simultaneously targets both PD-1 and PD-L1:
- Commenced GMP manufacturing campaign.
- Initiated preparation of IND submission materials with IND submission targeted for the first quarter of 2023.
Financial Highlights:
- Completed
$136 million in gross proceeds ($128 million net of expenses) follow-on public offering with top-tier life sciences focused investors. - Uplisted and initiated trading on the Nasdaq Capital Market under the symbol “CMPX”.
- Ended the year with
$144.5 million in cash and cash equivalents.
Other Business Updates:
- Acquired TRIGR Therapeutics for
$50.3 million in a stock-for-stock transaction and added CTX-009 to the pipeline. - Presented data from the Phase 1 study of CTX-009 at an oral plenary session at the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics (Abstract Number: 4749; Session title: Plenary Session 2: New Drugs on the Horizon I).
Financial Results for Fourth Quarter and Full Year Ended December 31, 2021
Net loss for the year ended December 31, 2021, was
Research and development (R&D) Expenses
R&D expenses were
General and Administrative (G&A) Expenses
G&A expenses were
Cash Position
As of December 31, 2021, cash and cash equivalents were
About Compass Therapeutics
Compass Therapeutics, Inc. is a clinical-stage oncology-focused biopharmaceutical company developing proprietary antibody-based therapeutics to treat multiple human diseases. Compass’s scientific focus is on the relationship between angiogenesis, the immune system, and tumor growth. The company pipeline of novel product candidates is designed to target multiple critical biological pathways required for an effective anti-tumor response. These include modulation of the microvasculature via angiogenesis-targeted agents, induction of a potent immune response via activators on effector cells in the tumor microenvironment, and alleviation of immunosuppressive mechanisms used by tumors to evade immune surveillance. Compass plans to advance its product candidates through clinical development as both standalone therapies and in combination with proprietary pipeline antibodies based on supportive clinical and nonclinical data. The company was founded in 2014 and is headquartered in Boston, Massachusetts. For more information, visit the Compass Therapeutics website at https://www.compasstherapeutics.com
Forward-Looking Statements
This press release contains forward-looking statements. Statements in this press release that are not purely historical are forward-looking statements. Such forward-looking statements include, among other things, references to the Company’s financial position to continue advancing its product candidates, expectations about the Company’s cash runway, business and development plans, and statements regarding the Company’s product candidates, their development, regulatory plans with respect thereto and therapeutic potential thereof, planned interactions with regulatory authorities, and planned clinical development. Actual results could differ from those projected in any forward-looking statements due to numerous factors. Such factors include, among others, the Company’s ability to raise the additional funding it will need to continue to pursue its business and product development plans, the inherent uncertainties associated with developing product candidates and operating as a development stage company, the Company’s ability to identify additional product candidates for development, the Company’s ability to develop, complete clinical trials for, obtain approvals for and commercialize any of our product candidates, competition in the industry in which the Company operates and market conditions. These forward-looking statements are made as of the date of this press release, and the Company assumes no obligation to update the forward-looking statements, or to update the reasons why actual results could differ from those projected in the forward-looking statements, except as required by law. Investors should consult all of the information set forth herein and should also refer to the risk factor disclosure set forth in the reports and other documents we file with the SEC available at www.sec.gov, including without limitation our Form 10-K for the year ended December 31, 2021, and our subsequent filings with the SEC.
Investor Contact
Vered Bisker-Leib, President & Chief Operating Officer
ir@compasstherapeutics.com
Media Contact
Anna Gifford, Communications Manager
media@compasstherapeutics.com
617-500-8099
Compass Therapeutics, Inc. and Subsidiaries | |||||||||||||||||
Consolidated Statements of Operations | |||||||||||||||||
(In thousands, except per share data) | |||||||||||||||||
Three Months Ended December 31, | Year Ended December 31, | ||||||||||||||||
2021 | 2020 | 2021 | 2020 | ||||||||||||||
Operating expenses: | |||||||||||||||||
Research and development | $ | 9,574 | $ | 4,406 | $ | 20,337 | $ | 14,904 | |||||||||
General and administrative | 3,426 | 3,544 | 10,927 | 12,908 | |||||||||||||
In-process R&D | — | — | 50,618 | — | |||||||||||||
Total operating expenses | 13,000 | 7,950 | 81,882 | 27,812 | |||||||||||||
Loss from operations | (13,000 | ) | (7,950 | ) | (81,882 | ) | (27,812 | ) | |||||||||
Other expense | 7 | (441 | ) | (299 | ) | (1,656 | ) | ||||||||||
Loss before income tax expense | (12,993 | ) | (8,391 | ) | (82,181 | ) | (29,468 | ) | |||||||||
Income tax expense | 13 | — | — | (32 | ) | ||||||||||||
Net loss | $ | (12,980 | ) | $ | (8,391 | ) | $ | (82,181 | ) | $ | (29,500 | ) | |||||
Net loss per share - basic and diluted | $ | (0.15 | ) | $ | (0.16 | ) | $ | (1.31 | ) | $ | (0.96 | ) | |||||
Basic and diluted weighted average shares outstanding | 88,255 | 51,052 | 62,870 | 30,776 | |||||||||||||
Compass Therapeutics, Inc. and Subsidiaries | |||||||||
Consolidated Balance Sheets | |||||||||
(In thousands, except per share data) | |||||||||
December 31, | |||||||||
2021 | 2020 | ||||||||
Assets | |||||||||
Current assets: | |||||||||
Cash and cash equivalents | $ | 144,514 | $ | 47,076 | |||||
Prepaid expenses and other current assets | 2,591 | 3,126 | |||||||
Total current assets | 147,105 | 50,202 | |||||||
Property and equipment, net | 2,243 | 1,126 | |||||||
Restricted cash | — | 263 | |||||||
Operating lease, right-of-use ("ROU") asset | 4,089 | — | |||||||
Other assets | 320 | 320 | |||||||
Total assets | $ | 153,757 | $ | 51,911 | |||||
Liabilities and Stockholders' Equity | |||||||||
Current liabilities: | |||||||||
Accounts payable | $ | 867 | $ | 1,061 | |||||
Accrued expenses | 8,775 | 1,571 | |||||||
Operating lease obligations, current portion | 989 | — | |||||||
Long-term debt, current portion | — | 7,467 | |||||||
Total current liabilities | 10,631 | 10,099 | |||||||
Long-term debt, net of current portion | — | 1,867 | |||||||
Operating lease obligations, net of long-term portion | 3,048 | — | |||||||
Total liabilities | 13,679 | 11,966 | |||||||
Commitments and Contingencies | |||||||||
Stockholders' equity: | |||||||||
Preferred stock, | — | — | |||||||
Common stock, | 10 | 5 | |||||||
Additional paid-in-capital | 373,657 | 191,348 | |||||||
Accumulated deficit | (233,589 | ) | (151,408 | ) | |||||
Total stockholders' equity | 140,078 | 39,945 | |||||||
Total liabilities and stockholders' equity | $ | 153,757 | $ | 51,911 | |||||
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