Codiak BioSciences Reports Fourth Quarter and Full Year 2021 Financial Results and Recent Operational Progress
Codiak BioSciences reported significant financial growth in its Q4 and full year 2021 results. Total revenues surged to $7.7 million for Q4 and $22.9 million for the year, primarily due to collaborations with Jazz and Sarepta. The company achieved a net income of $16.7 million for Q4, a turnaround from a net loss in 2020. R&D expenses rose to $17.4 million in Q4, reflecting ongoing development, while general and administrative costs increased to $6.9 million. Codiak anticipates further clinical data releases and IND application progress in 2022, positioning itself for future growth.
- Total revenues increased to $7.7 million in Q4 2021, up from $1.6 million in 2020.
- Annual revenues rose to $22.9 million from $2.9 million in 2020, marking significant growth.
- Achieved a net income of $16.7 million in Q4 2021, a significant turnaround from a net loss of $18.0 million in 2020.
- Projected promising data from exoSTING clinical trials and initiation of exoASO-STAT6 in 1H 2022.
- Net loss for the year was $37.2 million, despite a decrease from $91.7 million in 2020.
- R&D expenses increased to $17.4 million for Q4, indicating rising operational costs amid ongoing development challenges.
- General and administrative expenses rose to $6.9 million in Q4, reflecting the transition to a public company.
– Reported positive initial data from exoSTING™ clinical trial; on track to provide data from all dose escalation cohorts in late 1H 2022 –
– Investigational New Drug (IND) application cleared for exoASO™-STAT6, with clinical trial initiation expected 1H 2022 –
– Initial safety, PK/PD and efficacy data for exoIL-12™ in CTCL patients anticipated late 1H 2022 –
– Progressed preclinical pan-beta coronavirus vaccine program –
CAMBRIDGE, Mass., March 10, 2022 (GLOBE NEWSWIRE) -- Codiak BioSciences, Inc. (NASDAQ: CDAK), a clinical-stage biopharmaceutical company pioneering the development of exosome-based therapeutics as a new class of medicines, today reported fourth quarter and full year 2021 financial results and recent operational progress.
“We are making a strong start in 2022 thanks to progress with our development programs in 2021 and into this year, and plan to report clinical data for two of our engineered exosome therapeutic candidates and initiate clinical development for a third candidate all in the first half of the year,” said Douglas E. Williams, Ph.D., President and CEO of Codiak. “The platform we’ve developed at Codiak allows us to deliver multiple classes of therapeutics with a high degree of precision to specific cells and our clinical data from two programs has already shown promising safety and predictable PK/PD relationships. The emergence of programs in vaccines and gene delivery highlight the breadth of opportunity across multiple therapeutic areas with the engEx™ platform.”
Fourth Quarter 2021 and Recent Highlights
- Reported positive initial data from dose cohorts 1-3 in the Phase 1/2 clinical trial of exoSTING (CDK-002) for the treatment of advanced/metastatic, recurrent and injectable solid tumors; progressed subject dosing to cohorts 4 and 5 and follow-up in all dose cohorts
- Advanced cutaneous T cell lymphoma (CTCL) portion of Phase 1 trial of exoIL-12 (CDK-003)
- Filed and received U.S. FDA clearance of Investigational New Drug (IND) application for exoASO-STAT6 (CDK-004) for the intravenous treatment of hepatocellular carcinoma
- Presented three abstracts at the 36th Annual Meeting of the Society for Immunotherapy of Cancer (SITC 2021), including new preclinical data on exoASO-STAT6 in hepatocellular carcinoma, exoSTING in leptomeningeal disease and the combination of exoSTING and exoIL-12 in solid tumors
- Announced new preclinical data from the exoVACC™ exosome-based vaccine platform at the World Vaccine & Immunotherapy Congress (WVIC) 2021
- Published a manuscript describing the full exoASO-STAT6 preclinical program in the American Association for the Advancement of Science’s journal, Science Advances
Anticipated Milestones and Events
- Safety, PK, PD, and objective response rate (ORR) data from dose escalation cohorts 1-5 in the Phase 1/2 trial of exoSTING and recommended Phase 2 dose expected in late 1H 2022
- First-in-human dosing for exoASO-STAT6 in a Phase 1 clinical trial in hepatocellular carcinomas anticipated in 1H 2022
- Initial safety, PK/PD and efficacy data in CTCL patients in the Phase 1 clinical trial of exoIL-12 anticipated in late 1H 2022. While COVID-related restrictions in the UK that impacted clinical trial sites last year are abating, Codiak continues to work with those sites to explore options to facilitate enrollment.
- Poster presentation of preclinical data for exoASO-C/EBPb, a proprietary engineered exosome loaded with antisense oligonucleotides targeting C/EBPβ, at the American Association for Cancer Research (AACR) Annual Meeting, to be held April 8-13, 2022
- Presentation of new preclinical data from the exoVACC pan-beta coronavirus vaccine program, as part of Codiak’s collaboration with the Ragon Institute, at the World Vaccine Congress, to be held April 18-21, 2022
Fourth Quarter and Full Year 2021 Financial Results
Total revenues for the quarter ended December 31, 2021 were
Net income for the quarter ended December 31, 2021 was
Research and development expenses were
Research and development expenses were
General and administrative expenses were
As of December 31, 2021, Codiak had cash and cash equivalents of approximately
About Codiak BioSciences
Codiak is a clinical-stage biopharmaceutical company pioneering the development of exosome-based therapeutics, a new class of medicines with the potential to transform the treatment of a wide spectrum of diseases with high unmet medical need. By leveraging the biology of exosomes as natural intercellular transfer mechanisms, Codiak has developed its proprietary engEx Platform to expand upon the innate properties of exosomes to design, engineer and manufacture novel exosome therapeutic candidates. Codiak has utilized its engEx Platform to generate a deep pipeline of engineered exosomes aimed at treating a broad range of disease areas, spanning oncology, neuro-oncology, neurology, and infectious disease.
Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including, among other things, statements concerning the development and therapeutic potential of exoSTING and exoIL-12, including timing of release of data from clinical trials and the results of those trials, statements concerning the development of exoASO-STAT6, including the timing of IND filing and initiation of clinical trials, and statements regarding the capabilities and potential of Codiak’s engEx Platform and engineered exosomes generally. Any forward-looking statements in this press release are based on management’s current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. For a discussion of these risks and uncertainties, and other important factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in Codiak’s Annual Report on Form 10-K for the year ended December 31, 2021, and in subsequent filings with the Securities and Exchange Commission (SEC), as well as discussions of potential risks, uncertainties and other important factors in Codiak’s subsequent filings with the SEC. All information in this press release is current as of the date of this report, and Codiak undertakes no duty to update this information unless required by law.
- financial tables follow –
CODIAK BIOSCIENCES, INC. | ||||||||
CONSOLIDATED BALANCE SHEETS | ||||||||
(in thousands, except share and per share data) | ||||||||
YEAR ENDED DECEMBER 31, | ||||||||
2021 | 2020 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 76,938 | $ | 88,915 | ||||
Prepaid manufacturing services | 7,315 | 101 | ||||||
Prepaid expenses and other current assets | 5,918 | 4,742 | ||||||
Total current assets | 90,171 | 93,758 | ||||||
Property and equipment, net | 23,479 | 31,410 | ||||||
Restricted cash | 4,170 | 4,170 | ||||||
Operating right-of-use assets | 21,957 | 22,003 | ||||||
Prepaid manufacturing services, net of current portion | 31,893 | - | ||||||
Total assets | $ | 171,670 | $ | 151,341 | ||||
Liabilities and Stockholders’ Equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 1,838 | $ | 2,018 | ||||
Accrued expenses | 9,703 | 8,870 | ||||||
Deferred revenue | 12,963 | 5,281 | ||||||
Operating lease liabilities | 2,661 | 1,482 | ||||||
Total current liabilities | 27,165 | 17,651 | ||||||
Long-term liabilities: | ||||||||
Deferred revenue, net of current portion | 30,686 | 57,416 | ||||||
Note payable, net of discount | 25,430 | 24,960 | ||||||
Operating lease liabilities, net of current portion | 34,884 | 36,540 | ||||||
Other long-term liabilities | - | 207 | ||||||
Total liabilities | 118,165 | 136,774 | ||||||
Commitments and contingencies (Note 11) | ||||||||
Stockholders’ equity: | ||||||||
Common stock, | 2 | 2 | ||||||
Additional paid-in capital | 378,750 | 302,655 | ||||||
Accumulated deficit | (325,247 | ) | (288,090 | ) | ||||
Total stockholders’ equity | 53,505 | 14,567 | ||||||
Total liabilities and stockholders’ equity | $ | 171,670 | $ | 151,341 |
CODIAK BIOSCIENCES, INC. | ||||||||||||||||
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS | ||||||||||||||||
(in thousands, except share and per share data) | ||||||||||||||||
THREE MONTHS ENDED DECEMBER 31, | YEAR ENDED DECEMBER 31, | |||||||||||||||
2021 | 2020 | 2021 | 2020 | |||||||||||||
Revenue: | ||||||||||||||||
Collaboration revenue | $ | 7,697 | $ | 1,639 | $ | 22,935 | $ | 2,915 | ||||||||
Total revenue | 7,697 | 1,639 | 22,935 | 2,915 | ||||||||||||
Operating expenses: | ||||||||||||||||
Research and development | 17,419 | 13,328 | 64,855 | 73,981 | ||||||||||||
General and administrative | 6,919 | 5,919 | 27,629 | 19,852 | ||||||||||||
Total operating expenses | 24,338 | 19,247 | 92,484 | 93,833 | ||||||||||||
Loss from operations | (16,641 | ) | (17,608 | ) | (69,549 | ) | (90,918 | ) | ||||||||
Other income (expense): | ||||||||||||||||
Gain on disposition | 33,286 | - | 33,286 | - | ||||||||||||
Other income | 618 | 353 | 1,780 | 906 | ||||||||||||
Interest income | 4 | 7 | 22 | 253 | ||||||||||||
Interest expense | (605 | ) | (710 | ) | (2,696 | ) | (1,906 | ) | ||||||||
Total other income (expense), net | 33,303 | (350 | ) | 32,392 | (747 | ) | ||||||||||
Net income (loss) | $ | 16,662 | $ | (17,958 | ) | $ | (37,157 | ) | $ | (91,665 | ) | |||||
Cumulative dividends on redeemable convertible preferred stock | — | (534 | ) | — | (10,831 | ) | ||||||||||
Net income (loss) attributable to common stockholders | $ | 16,662 | $ | (18,492 | ) | $ | (37,157 | ) | $ | (102,496 | ) | |||||
Net income (loss) per share attributable to common stockholders, basic and diluted | $ | 0.74 | $ | (1.14 | ) | $ | (1.70 | ) | $ | (16.18 | ) | |||||
Weighted average common shares outstanding, basic and diluted | 22,373,607 | 16,233,377 | 21,794,546 | 6,332,841 | ||||||||||||
Comprehensive income (loss): | ||||||||||||||||
Net income (loss) | $ | 16,662 | $ | (17,958 | ) | $ | (37,157 | ) | $ | (91,665 | ) | |||||
Other comprehensive loss: | ||||||||||||||||
Unrealized loss on investments, net of tax of | — | — | — | (43 | ) | |||||||||||
Total other comprehensive loss | — | — | — | (43 | ) | |||||||||||
Comprehensive income (loss) | $ | 16,662 | $ | (17,958 | ) | $ | (37,157 | ) | $ | (91,708 | ) |
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