– Reported platform-validating initial data from Phase 1 studies of exoSTING™ and exoIL-12™; plans to initiate Phase 2 studies for both programs in 1H 2023 –
– Initiated patient dosing in Phase 1 clinical trial of exoASO™-STAT6 in patients with advanced hepatocellular carcinoma, liver metastases from primary gastric cancer and colorectal cancer –
– Partnered with CEPI to advance pan Betacoronavirus candidate –
– Presented positive preclinical data on the Company’s engEx-AAV™ discovery program –
“During the second quarter we made strong progress supporting our approach and making advancements across our pipeline. We reported Phase 1 data sets from both our exoSTING™ and exoIL-12™ programs, further validating our engEx® platform, and demonstrating we were able to deliver repeat doses of exoSTING™ and exoIL-12™ to the tumor with a high level of specificity. Importantly, we did so with no observed systemic exposure or associated toxicity, and an enhanced therapeutic index – while demonstrating tumor shrinkage in both injected and uninjected lesions,” said
Second Quarter 2022 and Recent Highlights
- Announced platform-validating data from Phase 1 trials of exoSTING™ and exoIL-12™; both candidates demonstrated potential for best-in-class profile; Codiak has identified a recommended Phase 2 dose for each program and intends to finalize study plans with the FDA during the second half of this year to prepare for initiation of Phase 2 trials for both candidates early next year.
- In a Phase 1 trial, exoIL-12™ demonstrated a differentiating safety and tolerability profile, with no detectable systemic exposure of IL-12 and no treatment-related adverse events, which has not previously been reported by others with recombinant IL-12. The two patients with cutaneous T cell lymphoma (CTCL) who have been treated each received multiple (>20) injections of exoIL-12 and experienced tumor regressions in both injected and non-injected lesions, including a partial response in one patient.
- In the Phase 1/2 clinical trial evaluating exoSTING™ as a single agent in patients with late-stage refractory solid tumors, data across all five dose cohorts showed repeat doses of exoSTING™ were well-tolerated, demonstrated tumor retention with no systemic exposure of the
STING agonist, and in a subset of patients, tumor shrinkage was observed in injected and uninjected lesions.
- Initiated patient dosing in the Phase 1 clinical trial of exoASO™-STAT6 in patients with advanced hepatocellular carcinoma, liver metastases from primary gastric cancer and colorectal cancer; exoASO™-STAT6 is Codiak’s third clinical program and the first to evaluate a systemically administered exosome-based drug candidate.
- Partnered with CEPI to continue the advancement of vaccine candidates from the Company’s pan Betacoronavirus program; as part of the partnership, CEPI will provide seed funding of up to
$2.5 million , which Codiak anticipates will fund the completion of preclinical development and identification of a clinical candidate. - Presented preclinical data on the Company’s engEx-AAV™ discovery program, a novel strategy that aims to leverage exosomes to improve adeno-associated virus (AAV) vector gene therapy, at the 25th Annual Meeting of the
American Society of Gene andCell Therapy (ASGCT); data demonstrated that exosome engineering generates significant increases in AAV yield compared to unmodified exosomes, while retaining the functionality to transduce cells with AAV and resist neutralizing antibodies that impair gene therapy efficacy.
Anticipated Milestones and Events
- Initiate Phase 2 study of exoIL-12™ in an expanded group of tumor types in 1H 2023; continue to monitor patients enrolled in Phase 1 study.
- Initiate Phase 2 study of exoSTING™ in bladder cancer in 1H 2023; continue to monitor patients enrolled in ongoing Phase 1/2 study, reporting additional data at an upcoming scientific conference.
- Continue enrollment for ongoing Phase 1 trial for exoASO™-STAT6, with initial data expected in 1H 2023.
- Advance exoVACC™ pan Betacoronavirus program toward identification of a clinical candidate through new partnership with CEPI.
Second Quarter 2022 Financial Results
Total revenues for the quarter ended
Net loss for the quarter ended
Research and development expenses were
General and administrative expenses were
As of
About
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, infectious disease and rare 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 initiation of clinical trials, the release of data from clinical trials and the results of those trials, statements concerning the clinical development of exoASO™-STAT6, 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. In particular, the statements regarding the initiation and timing of clinical trials are dependent upon availability of sufficient cash resources, as to which the Company can make no assurance. 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
- financial tables follow -
CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands, except share and per share data)
(unaudited)
2022 | 2021 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 41,785 | $ | 76,938 | ||||
Prepaid manufacturing expenses | 9,063 | 7,315 | ||||||
Prepaid expenses and other current assets | 5,161 | 5,918 | ||||||
Total current assets | 56,009 | 90,171 | ||||||
Property and equipment, net | 21,557 | 23,479 | ||||||
Restricted cash | 4,170 | 4,170 | ||||||
Operating right-of-use assets | 21,304 | 21,957 | ||||||
Prepaid manufacturing expenses, net of current portion | 29,670 | 31,893 | ||||||
Total assets | $ | 132,710 | $ | 171,670 | ||||
Liabilities and Stockholders’ Equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 1,131 | $ | 1,838 | ||||
Accrued expenses | 7,699 | 9,703 | ||||||
Deferred revenue | 292 | 12,963 | ||||||
Operating lease liabilities | 2,891 | 2,661 | ||||||
Total current liabilities | 12,013 | 27,165 | ||||||
Long-term liabilities: | ||||||||
Deferred revenue, net of current portion | 17,341 | 30,686 | ||||||
Note payable, net of discount | 25,596 | 25,430 | ||||||
Operating lease liabilities, net of current portion | 33,362 | 34,884 | ||||||
Other long-term liabilities | - | - | ||||||
Total liabilities | 88,312 | 118,165 | ||||||
Commitments and contingencies | ||||||||
Stockholders’ equity: | ||||||||
Common stock, | 2 | 2 | ||||||
Additional paid-in capital | 384,446 | 378,750 | ||||||
Accumulated deficit | (340,050 | ) | (325,247 | ) | ||||
Total stockholders’ equity | 44,398 | 53,505 | ||||||
Total liabilities and stockholders’ equity | $ | 132,710 | $ | 171,670 |
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(In thousands, except share and per share data)
(unaudited)
THREE MONTHS ENDED | SIX MONTHS ENDED | |||||||||||||||
2022 | 2021 | 2022 | 2021 | |||||||||||||
Revenue: | ||||||||||||||||
Collaboration revenue | $ | 13,145 | $ | 890 | $ | 25,849 | $ | 14,081 | ||||||||
Total revenue | 13,145 | 890 | 25,849 | 14,081 | ||||||||||||
Operating expenses: | ||||||||||||||||
Research and development | 12,798 | 15,419 | 27,045 | 31,969 | ||||||||||||
General and administrative | 7,364 | 6,937 | 14,071 | 13,525 | ||||||||||||
Total operating expenses | 20,162 | 22,356 | 41,116 | 45,494 | ||||||||||||
Loss from operations | (7,017 | ) | (21,466 | ) | (15,267 | ) | (31,413 | ) | ||||||||
Other income (expense): | ||||||||||||||||
Interest expense | (649 | ) | (704 | ) | (1,250 | ) | (1,401 | ) | ||||||||
Interest income | 34 | 9 | 38 | 14 | ||||||||||||
Other income | 848 | 352 | 1,667 | 683 | ||||||||||||
Realized gain | 9 | - | 9 | - | ||||||||||||
Total other income (expense), net | 242 | (343 | ) | 464 | (704 | ) | ||||||||||
Net loss | $ | (6,775 | ) | $ | (21,809 | ) | $ | (14,803 | ) | $ | (32,117 | ) | ||||
Net loss per share attributable to common stockholders, basic and diluted | $ | (0.30 | ) | $ | (0.99 | ) | $ | (0.66 | ) | $ | (1.51 | ) | ||||
Weighted average common shares outstanding, basic and diluted | 22,493,879 | 22,117,593 | 22,444,799 | 21,230,424 |
Investor Contact:
VP, Investor Relations and Corporate Communications
T: 617-949-4220
E: investor@codiakbio.com
Media Contact:
Scient PR
E: media@codiakbio.com
Source:
2022 GlobeNewswire, Inc., source