CARTESIAN THERAPEUTICS, INC. Topline data from Phase 2b study of Descartes-08, the Company’s potential first-in-class mRNA CAR-T cell therapy, in myasthenia gravis (MG) remains on track for mid-2024
On track to initiate Phase 2 study of Descartes-08 in systemic lupus erythematosus (SLE) in 1H24 as well as Phase 2 basket studies in additional autoimmune indications in 2H24
Following recent IND clearance, planning underway for first-in-human Phase 1 dose escalation study of Descartes-15, a next-generation mRNA CAR-T product candidate
Approximately
“With several potentially value-creating milestones anticipated throughout the year ahead, we are making strong progress in our mission to deliver innovative cell therapies to patients suffering from autoimmune diseases,” said
Recent Pipeline Progress and Anticipated Milestones
- Topline Data from Randomized Phase 2b Study of Descartes-08 in Patients with MG Expected for Mid-2024. Enrollment remains ongoing in the Company’s Phase 2b randomized, double-blind, placebo-controlled trial of Descartes-08 in patients with MG (NCT04146051), with topline results expected in mid-2024.
- Announced Positive Long-Term Follow-Up Data from Phase 2a Study of Descartes-08 in Patients with MG. In
January 2024 , Cartesian announced positive twelve-month follow-up data from its Phase 2a study of Descartes-08, the Company’s autologous anti-B cell maturation antigen (BCMA) mRNA CAR-T cell therapy product candidate, in patients with generalized MG, a chronic autoimmune disorder that causes disabling muscle weakness and fatigue. In this study, Descartes-08 was administered in an outpatient setting without integrating vectors or preconditioning chemotherapy, and durable depletion of autoantibodies and clinically meaningful improvements in MG severity scores during the one-year follow-up period were observed. Descartes-08 was observed to be well-tolerated, with no dose-limiting toxicities, cytokine release syndrome, or neurotoxicity.
Descartes-08 has been granted Orphan Drug Designation by theU.S. Food and Drug Administration (FDA) for the treatment of MG.
- Initiation of Phase 2 Study of Descartes-08 in Patients with SLE Expected for First Half of 2024. The Company expects to initiate a Phase 2 study of Descartes-08 in patients with SLE (NCT06038474) in the first half of 2024. The Phase 2 study, for which the Company has received investigational new drug (IND) clearance, is designed to assess the safety and tolerability of outpatient Descartes-08 administration without preconditioning chemotherapy. SLE is an incurable autoimmune disease marked by systemic inflammation that affects multiple organ systems. It is estimated to impact approximately 1.5 million people in
the United States . - IND Application Cleared for Descartes-15. In
January 2024 , Cartesian announced that the FDA cleared its IND application for Descartes-15, a next-generation, autologous anti-BCMA mRNA CAR-T product candidate. As with Descartes-08, Descartes-15 is designed not to require preconditioning chemotherapy, has been observed to have predictable and controllable pharmacokinetics and is designed to avoid the risk of genomic integration. Planning for the first-in-human Phase 1 dose escalation study is underway. The study is designed to assess the safety and tolerability of outpatient Descartes-15 administration in patients with multiple myeloma. The Company expects to subsequently assess Descartes-15 in autoimmune indications.
Corporate Update
- Upcoming Special Meeting of Stockholders Seeking to Approve Preferred Stock Conversion and Reverse Stock Split. Cartesian plans to hold a special meeting of stockholders on
March 27, 2024 to seek stockholder approval for the conversion of the Company’s Series A Non-Voting Convertible Preferred Stock into the Company’s common stock and a reverse stock split at a ratio in the range of 1-for-20 and 1-for-30. The reverse stock split would impact all holders of Cartesian common stock proportionally and would not impact any stockholder’s percentage ownership of common stock. Holders of common stock of record as ofFebruary 13, 2024 are eligible to vote at the meeting. - Announced Plans to Transition Corporate Headquarters to
Frederick, Maryland . The Company recently announced plans to transition its corporate headquarters toFrederick, Maryland . The approximately 20,000 square foot state-of-the-art current good manufacturing practice (cGMP) compliant facility has clinical and commercial manufacturing scale capabilities designed to support the Company's maturing pipeline. - Completed Merger with
Selecta Biosciences, Inc. and Concurrent$60.25 Million Private Financing. InNovember 2023 , Cartesian announced its merger withSelecta Biosciences, Inc. , creating a fully integrated, publicly traded company pioneering mRNA cell therapy for the treatment of autoimmune diseases. In connection with the merger, Cartesian announced a$60.25 million private financing led byTimothy A. Springer , Ph.D.
Full Year 2023 Financial Results
- Pro forma cash, cash equivalents, and restricted cash of approximately
$118.3 million as ofDecember 31, 2023 , which reflects net proceeds received in the first quarter of 2024 from theNovember 2023 financing. The Company’s pro forma cash and cash equivalents as ofDecember 31, 2023 , is expected to support planned operations and the development of Cartesian’s pipeline into the second half of 2026, through the Phase 3 study of lead candidate, Descartes-08. - Research and development expenses were
$71.8 million for the year endedDecember 31, 2023 , compared to$72.4 million for the year endedDecember 31, 2022 . The decrease in expense of$0.6 million for the year endedDecember 31, 2023 was primarily due to reductions in expenses incurred for preclinical and clinical programs due to the strategic reprioritization partially offset by expenses incurred for stock compensation and personnel expenses. - General and administrative expenses were
$40.6 million for the year endedDecember 31, 2023 , compared to$23.9 million for the year endedDecember 31, 2022 . The increase in expense of$16.7 million for the year endedDecember 31, 2023 was primarily due to expenses incurred for stock compensation, personnel expenses, and professional fees incurred in connection with the merger. - Net loss was
$(219.7) million , or$(1.66) net loss per share (basic/diluted), for the year endedDecember 31, 2023 , compared to net income of$35.4 million , or$0.24 net income per share (basic), for the year endedDecember 31, 2022 .
About Cartesian Therapeutics
Cartesian Therapeutics is a clinical-stage company pioneering mRNA cell therapies for the treatment of autoimmune diseases. The Company’s lead asset, Descartes-08, is a potential first-in-class mRNA CAR-T in Phase 2b clinical development for patients with generalized myasthenia gravis. Additional Phase 2 studies are planned in systemic lupus erythematosus under an allowed IND, as well as basket trials in additional autoimmune indications. The Company’s clinical-stage pipeline also includes Descartes-15, a next-generation, autologous anti-BCMA mRNA CAR-T. For more information, please visit www.cartesiantherapeutics.com or follow the Company on LinkedIn or X, formerly known as Twitter.
Forward Looking Statements
Any statements in this press release about the future expectations, plans and prospects of the Company, including without limitation, statements regarding the Company’s expected cash resources and cash runway, the Company’s estimated cash on hand, the conversion of the Company’s Series A Non-Voting Convertible Preferred Stock, the Company’s plans to conduct a reverse stock split pending stockholder approval, the Company’s headquarters relocation, the Company’s manufacturing capabilities and ability to supply necessary quantities of its product candidates for clinical trials and potential commercialization, the Company’s ability to maintain control over its product quality and production, the potential of RNA Armory® to enable precision control and optimization of engineered cells for diverse cell therapies leveraging multiple modalities, the potential of Descartes-08 and Descartes-15 and the Company’s other product candidates to treat myasthenia gravis, systemic lupus erythematosus, or any other disease, the anticipated initiation timing of planned clinical trials, the anticipated timing or the outcome of ongoing and planned clinical trials, studies and data readouts, the anticipated timing or the outcome of the FDA’s review of the Company’s regulatory filings, the Company’s ability to conduct its clinical trials and preclinical studies, the timing or making of any regulatory filings, the anticipated timing or outcome of selection of developmental product candidates, the ability of the Company to consummate any expected agreements and licenses and to realize the anticipated benefits thereof, the novelty of treatment paradigms that the Company is able to develop, the potential of any therapies developed by the Company to fulfill unmet medical needs, the Company’s ability to enter into and maintain its strategic partnerships, and enrollment in the Company’s clinical trials and other statements containing the words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “hypothesize,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “would,” and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including, but not limited to, the following: the uncertainties inherent in the initiation, completion and cost of clinical trials including proof of concept trials, including uncertain outcomes, the availability and timing of data from ongoing and future clinical trials and the results of such trials, whether preliminary results from a particular clinical trial will be predictive of the final results of that trial and whether results of early clinical trials will be indicative of the results of later clinical trials, the ability to predict results of studies performed on human beings based on results of studies performed on non-human subjects, the unproven approach of the Company’s RNA Armory® technology, potential delays in enrollment of patients, undesirable side effects of the Company’s product candidates, its reliance on third parties to conduct its clinical trials, the Company’s inability to maintain its existing or future collaborations, licenses or contractual relationships, its inability to protect its proprietary technology and intellectual property, potential delays in regulatory approvals, the availability of funding sufficient for its foreseeable and unforeseeable operating expenses and capital expenditure requirements, the Company’s recurring losses from operations and negative cash flows, substantial fluctuation in the price of the Company’s common stock, risks related to geopolitical conflicts and pandemics and other important factors discussed in the “Risk Factors” section of the Company’s most recent Annual Report on Form 10-K and subsequently filed Quarterly Reports on Form 10-Q, and in other filings that the Company makes with the
| Consolidated Balance Sheets | |||||||
| (Amounts in thousands, except share data and par value) | |||||||
| 2023 | 2022 | ||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 76,911 | $ | 106,438 | |||
| Marketable securities | — | 28,164 | |||||
| Accounts receivable | 5,870 | 6,596 | |||||
| Unbilled receivables | 2,981 | 3,162 | |||||
| Prepaid expenses and other current assets | 4,967 | 3,778 | |||||
| Total current assets | 90,729 | 148,138 | |||||
| Non-current assets: | |||||||
| Property and equipment, net | 2,113 | 2,794 | |||||
| Right-of-use asset, net | 10,068 | 11,617 | |||||
| In-process research and development assets | 150,600 | — | |||||
| 48,163 | — | ||||||
| Long-term restricted cash | 1,377 | 1,311 | |||||
| Investments | 2,000 | 2,000 | |||||
| Other assets | — | 26 | |||||
| Total assets | $ | 305,050 | $ | 165,886 | |||
| Liabilities, convertible preferred stock, and stockholders’ (deficit) equity | |||||||
| Current liabilities: | |||||||
| Accounts payable | $ | 3,150 | $ | 316 | |||
| Accrued expenses and other current liabilities | 15,572 | 14,084 | |||||
| Loan payable | — | 8,476 | |||||
| Lease liability | 2,166 | 1,608 | |||||
| Deferred revenue | 2,311 | 593 | |||||
| Warrant liabilities | 720 | — | |||||
| Contingent value right liability | 15,983 | — | |||||
| Forward contract liabilities | 28,307 | — | |||||
| Total current liabilities | 68,209 | 25,077 | |||||
| Non-current liabilities: | |||||||
| Loan payable, net of current portion | — | 17,786 | |||||
| Lease liability, net of current portion | 8,789 | 10,055 | |||||
| Deferred revenue, net of current portion | 3,538 | — | |||||
| Warrant liabilities, net of current portion | 5,674 | 19,140 | |||||
| Contingent value right liability, net of current portion | 342,617 | — | |||||
| Deferred tax liabilities, net | 15,853 | — | |||||
| Total liabilities | 444,680 | 72,058 | |||||
| Series A Preferred Stock, | 296,851 | — | |||||
| Options for Series A Preferred Stock | 3,703 | — | |||||
| Stockholders’ (deficit) equity: | |||||||
| Preferred stock, | — | — | |||||
| Common stock, | 16 | 15 | |||||
| Additional paid-in capital | 179,047 | 493,308 | |||||
| Accumulated deficit | (614,647 | ) | (394,937 | ) | |||
| Accumulated other comprehensive loss | (4,600 | ) | (4,558 | ) | |||
| Total stockholders’ (deficit) equity | (440,184 | ) | 93,828 | ||||
| Total liabilities, convertible preferred stock, and stockholders’ (deficit) equity | $ | 305,050 | $ | 165,886 | |||
| Cartesian Therapeutics, Inc. and Subsidiaries | |||||||||||
| Consolidated Statements of Operations and Comprehensive Income (Loss) | |||||||||||
| (Amounts in thousands, except share and per share data) | |||||||||||
| Year Ended | |||||||||||
| 2023 | 2022 | 2021 | |||||||||
| Collaboration and license revenue | $ | 26,004 | $ | 110,777 | $ | 85,077 | |||||
| Operating expenses: | |||||||||||
| Research and development | 71,839 | 72,377 | 68,736 | ||||||||
| General and administrative | 40,581 | 23,862 | 20,938 | ||||||||
| Total operating expenses | 112,420 | 96,239 | 89,674 | ||||||||
| Operating (loss) income | (86,416 | ) | 14,538 | (4,597 | ) | ||||||
| Investment income | 4,964 | 2,073 | 44 | ||||||||
| Foreign currency transaction gain (loss), net | 38 | (22 | ) | — | |||||||
| Interest expense | (2,833 | ) | (3,031 | ) | (2,844 | ) | |||||
| Change in fair value of warrant liabilities | 12,746 | 20,882 | (2,339 | ) | |||||||
| Change in fair value of contingent value right liability | (18,300 | ) | — | — | |||||||
| Change in fair value of forward contract liabilities | (149,600 | ) | — | — | |||||||
| Other income, net | 691 | 330 | 15 | ||||||||
| (Loss) income) before income taxes | (238,710 | ) | 34,770 | (9,721 | ) | ||||||
| Income tax benefit (expense) | 19,000 | 609 | (15,966 | ) | |||||||
| Net (loss) income | (219,710 | ) | 35,379 | (25,687 | ) | ||||||
| Other comprehensive (loss) income: | |||||||||||
| Foreign currency translation adjustment | (53 | ) | 18 | (2 | ) | ||||||
| Unrealized gain (loss) on marketable securities | 11 | (10 | ) | (1 | ) | ||||||
| Total comprehensive (loss) income | $ | (219,752 | ) | $ | 35,387 | $ | (25,690 | ) | |||
| Net (loss) income per share: | |||||||||||
| Basic | $ | (1.66 | ) | $ | 0.24 | $ | (0.22 | ) | |||
| Diluted | $ | (1.66 | ) | $ | 0.10 | $ | (0.22 | ) | |||
| Weighted-average common shares outstanding: | |||||||||||
| Basic | 155,109,561 | 144,758,555 | 114,328,798 | ||||||||
| Diluted | 155,109,561 | 145,874,889 | 114,328,798 | ||||||||
Contact Information:
Investor Relations:
cartesian@argotpartners.com
Media:
david.rosen@argotpartners.com
2024 GlobeNewswire, Inc., source
