Celcuity Inc. Reports First Quarter Financial Results and Provides Corporate Update
Celcuity Inc. (Nasdaq: CELC) reported its first-quarter financial results and provided a corporate update. The Phase 3 VIKTORIA-1 trial remains on track, with topline data expected in the second half of 2024. The company also initiated a Phase 1b/2 trial for gedatolisib in prostate cancer, and dosed its first patient in February 2024. Financial highlights include a net loss of $21.6 million ($0.64 per share) for Q1 2024, compared to $11.9 million ($0.55 per share) in Q1 2023. Operating expenses rose to $22.5 million from $12.6 million year-over-year. Cash reserves stand at $177.7 million, expected to fund operations into early 2026.
- Phase 3 VIKTORIA-1 trial remains on track with topline data expected in H2 2024.
- Initiated Phase 1b/2 trial for gedatolisib in prostate cancer, with first patient dosed in February 2024.
- Cash reserves of $177.7 million expected to fund operations into early 2026.
- Net loss increased to $21.6 million in Q1 2024 from $11.9 million in Q1 2023.
- Operating expenses rose significantly to $22.5 million from $12.6 million year-over-year.
- Research and development expenses nearly doubled to $20.7 million in Q1 2024.
Insights
Celcuity's first quarter financial results showcase a significant increase in operating expenses, with a marked rise in Research and Development (R&D) expenses from $11.3 million to $20.7 million YoY. This substantial increase is mainly attributed to the VIKTORIA-1 Phase 3 trial and the CELC-G-201 Phase 1b/2 trial. Net loss for the quarter also widened from $11.9 million to $21.6 million. However, the company holds a significant cash reserve of $177.7 million, which provides a runway into the first half of 2026. From an investor perspective, while the cash position is strong, the increase in net loss may be concerning. It's important to monitor how effectively the company uses its capital to push its clinical trials forward, aiming for favorable outcomes and potential commercialization.
The announcement that the VIKTORIA-1 Phase 3 trial is on track to report topline data in the second half of 2024 for the PIK3CA wild type patient sub-group is a significant milestone. This trial could lead to critical insights into gedatolisib's efficacy in HR+, HER2- advanced breast cancer patients. Similarly, the initiation of the Phase 1b/2 trial for metastatic castration-resistant prostate cancer (mCRPC) and the dosing of the first patient mark important progress in expanding gedatolisib’s potential applications. Investors should focus on these trials' progress, as successful results could significantly enhance the company's value proposition and market potential.
The recent addition of a Chief Commercial Officer to Celcuity's executive team highlights the company's forward-looking strategy in preparing for the potential commercial launch of gedatolisib. This strategic move is essential as it aligns with the company's clinical advancements and upcoming data readouts. For retail investors, this indicates that Celcuity is not only focused on clinical development but also on market positioning and commercialization strategies. The potential market entry of gedatolisib, if successful, could position Celcuity as a competitive player in the oncology space, potentially driving long-term growth and shareholder value.
- The Phase 3 VIKTORIA-1 trial remains on track to report topline data from PIK3CA wild type patient sub-group in the second half of 2024
- First patient dosed in a Phase 1b/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer
$177.7 million in cash, cash equivalents and short-term investments expected to provide runway into the first half of 2026- Management to host webcast and conference call today, May 15, 2024, at 4:30 p.m. ET
MINNEAPOLIS, May 15, 2024 (GLOBE NEWSWIRE) -- Celcuity Inc. (Nasdaq: CELC), a clinical-stage biotechnology company pursuing development of targeted therapies for oncology, today announced financial results for the first quarter ended March 31, 2024 and other recent business developments.
“We continued to execute well this quarter. Our VIKTORIA-1 study remains on-track, and we dosed the first patient in our Phase 1b/2 trial in metastatic castration resistant prostate cancer,” said Brian Sullivan, Celcuity’s Chief Executive Officer and co-founder. “With the addition of a Chief Commercial Officer to our executive team, we began the foundational work needed to prepare for the potential commercial launch of gedatolisib. We look forward to presenting topline data from the PIK3CA wild type patient sub-group later this year.”
First Quarter 2024 Business Highlights and Other Recent Developments
- The VIKTORIA-1 Phase 3 trial remains on track to provide topline data for the PIK3CA wild type patient sub-group in the second half of 2024 and for the PIK3CA mutant patient sub-group in the first half of 2025.
- VIKTORIA-1 is evaluating gedatolisib in combination with fulvestrant with and without palbociclib in adults with HR+, HER2- advanced breast cancer who have received prior treatment with a CDK4/6 inhibitor.
- The Phase 3 VIKTORIA-1 clinical trial is enrolling patients at approximately 220 sites in 23 countries in North and South America, Europe, and Asia.
- The Phase 1b/2 clinical trial evaluating gedatolisib in combination with darolutamide for the treatment of metastatic castration resistant prostate cancer (mCRPC) was initiated in the fourth quarter of 2023. In February 2024, the first patient was dosed.
- Enrollment is ongoing and the trial is expected to enroll up to 54 patients with mCRPC whose disease progressed after treatment with an androgen receptor signaling inhibitor.
- The Phase 1b/2 trial is on track to provide initial preliminary data in the first half of 2025.
- In February 2024, the Company appointed Eldon Mayer as Chief Commercial Officer to enable Celcuity to begin laying the groundwork for the potential commercial launch of gedatolisib.
First Quarter 2024 Financial Results
Unless otherwise stated, all comparisons are for the first quarter ended March 31, 2024, compared to the first quarter ended March 31, 2023.
Total operating expenses were
Research and development (R&D) expenses were
General and administrative (G&A) expenses were
Net loss for the first quarter of 2024 was
Net cash used in operating activities for the first quarter of 2024 was
At March 31, 2024, Celcuity reported cash, cash equivalents and short-term investments of
Webcast and Conference Call Information
The Celcuity management team will host a webcast/conference call at 4:30 p.m. ET today to discuss the first quarter 2024 financial results and provide a corporate update. To participate in the teleconference, domestic callers should dial 1-888-886-7786 or 1-416-764-8658. A live webcast presentation can also be accessed using this weblink: https://viavid.webcasts.com/starthere.jsp?ei=1664947&tp_key=8c4820dec8. A replay of the webcast will be available on the Celcuity website following the live event.
About Celcuity
Celcuity is a clinical-stage biotechnology company focused on development of targeted therapies for treatment of multiple solid tumor indications. The company's lead therapeutic candidate is gedatolisib, a potent, pan-PI3K and mTOR inhibitor. Its mechanism of action and pharmacokinetic properties are highly differentiated from other currently approved and investigational therapies that target PI3K or mTOR alone or together. A Phase 3 clinical trial, VIKTORIA-1, evaluating gedatolisib in combination with fulvestrant with or without palbociclib in patients with HR+/HER2- advanced breast cancer is currently enrolling patients. More detailed information about the VIKTORIA-1 study can be found at ClinicalTrials.gov. A Phase 1b/2 clinical trial, CELC-G-201, evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is enrolling patients. The company's CELsignia companion diagnostic platform is uniquely able to analyze live patient tumor cells to identify new groups of cancer patients likely to benefit from already approved targeted therapies. Further information about Celcuity can be found at www.celcuity.com. Follow us on LinkedIn and Twitter.
Forward-Looking Statements
This press release contains statements that constitute "forward-looking statements" including, but not limited to, the design of our clinical trials; the timing of initiating and enrolling patients in, and receiving results and data from, our clinical trials; the costs and expected results from any ongoing or planned clinical trials; the market opportunity for gedatolisib; our strategy, marketing and commercialization plans; other expectations with respect to Celcuity's lead product candidate, gedatolisib, and its CELsignia platform; our anticipated use of cash; and the strength of our balance sheet. In some cases, you can identify forward-looking statements by terminology such as "may," "should," "expects," "plans," "anticipates," "believes," "estimates," "predicts," "potential," "intends" or "continue," and other similar expressions that are predictions of or indicate future events and future trends, or the negative of these terms or other comparable terminology. Forward-looking statements are subject to numerous risks, uncertainties, and conditions, many of which are beyond the control of Celcuity. These include, but are not limited to, unforeseen delays in our clinical trials, our ability to obtain and maintain regulatory approvals to commercialize our products, and the market acceptance of such products, the development of therapies and tools competitive with our products, and those risks set forth in the Risk Factors section in Celcuity's Annual Report on Form 10-K for the year ended December 31, 2023 filed with the Securities and Exchange Commission on March 27, 2024. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. Celcuity undertakes no obligation to update these statements for revisions or changes after the date of this press release, except as required by law.
View source version of release on GlobeNewswire.com
Contacts:
Celcuity Inc.
Brian Sullivan, bsullivan@celcuity.com
Vicky Hahne, vhahne@celcuity.com
(763) 392-0123
ICR Westwicke
Maria Yonkoski, maria.yonkoski@westwicke.com
(203) 682-7167
| Celcuity Inc. | |||||||
| Condensed Balance Sheets | |||||||
| March 31, 2024 | December 31, 2023 | ||||||
| (unaudited) | |||||||
| Assets | |||||||
| Current Assets: | |||||||
| Cash and cash equivalents | $ | 31,214,741 | $ | 30,662,774 | |||
| Investments | 146,447,843 | 149,919,974 | |||||
| Other current assets | 9,860,535 | 10,007,849 | |||||
| Total current assets | 187,523,119 | 190,590,597 | |||||
| Property and equipment, net | 306,024 | 228,782 | |||||
| Operating lease right-of-use assets | 351,911 | 400,019 | |||||
| Total Assets | $ | 188,181,054 | $ | 191,219,398 | |||
| Liabilities and Stockholders' Equity: | |||||||
| Current Liabilities: | |||||||
| Accounts payable | $ | 5,276,690 | $ | 5,076,699 | |||
| Operating lease liabilities | 181,882 | 184,950 | |||||
| Accrued expenses | 11,237,509 | 8,927,094 | |||||
| Total current liabilities | 16,696,081 | 14,188,743 | |||||
| Operating lease liabilities | 182,079 | 225,922 | |||||
| Note payable, non-current | 37,566,230 | 37,035,411 | |||||
| Total Liabilities | 54,444,390 | 51,450,076 | |||||
| Stockholders' Equity: | |||||||
| Preferred stock | 505 | 854 | |||||
| Common stock | 30,774 | 25,506 | |||||
| Additional paid-in capital | 315,393,843 | 299,818,965 | |||||
| Accumulated deficit | (181,688,458 | ) | (160,076,003 | ) | |||
| Total Stockholders' Equity | 133,736,664 | 139,769,322 | |||||
| Total Liabilities and Stockholders' Equity | $ | 188,181,054 | $ | 191,219,398 | |||
| Celcuity Inc. | |||||||
| Condensed Statements of Operations | |||||||
| (unaudited) | |||||||
| Three Months Ended March 31, | |||||||
| 2024 | 2023 | ||||||
| Operating expenses: | |||||||
| Research and development | $ | 20,647,559 | $ | 11,278,493 | |||
| General and administrative | 1,846,276 | 1,269,044 | |||||
| Total operating expenses | 22,493,835 | 12,547,537 | |||||
| Loss from operations | (22,493,835 | ) | (12,547,537 | ) | |||
| Other income (expense) | |||||||
| Interest expense | (1,400,712 | ) | (1,242,012 | ) | |||
| Interest income | 2,282,092 | 1,851,132 | |||||
| Other income (expense), net | 881,380 | 609,120 | |||||
| Net loss before income taxes | (21,612,455 | ) | (11,938,417 | ) | |||
| Income tax benefits | - | - | |||||
| Net loss | $ | (21,612,455 | ) | $ | (11,938,417 | ) | |
| Net loss per share, basic and diluted | $ | (0.64 | ) | $ | (0.55 | ) | |
| Weighted average common shares outstanding, basic and diluted | 33,612,054 | 21,680,877 | |||||
Cautionary Statement Regarding Non-GAAP Financial Measures
This press release contains references to non-GAAP adjusted net loss and non-GAAP adjusted net loss per share. Management believes these non-GAAP financial measures are useful supplemental measures for planning, monitoring, and evaluating operational performance as they exclude stock-based compensation expense, non-cash interest expense, and non-cash interest income from net loss and net loss per share. Management excludes these items because they do not impact Celcuity’s cash position, which management believes better enables Celcuity to focus on cash used in operations. However, non-GAAP adjusted net loss and non-GAAP adjusted net loss per share are not recognized measures under GAAP and do not have a standardized meaning prescribed by GAAP. As a result, management’s method of calculating non-GAAP adjusted net loss and non-GAAP adjusted net loss per share may differ materially from the method used by other companies. Therefore, non-GAAP adjusted net loss and non-GAAP adjusted net loss per share may not be comparable to similarly titled measures presented by other companies. Investors are cautioned that non-GAAP adjusted net loss and non-GAAP adjusted net loss per share should not be construed as alternatives to net loss, net loss per share or other statements of operations data (which are determined in accordance with GAAP) as an indicator of Celcuity’s performance or as a measure of liquidity and cash flows.
| Celcuity Inc. | |||||||
| Reconciliation of GAAP Net Loss to Non-GAAP Adjusted Net Loss and | |||||||
| GAAP Net Loss Per Share to Non-GAAP Adjusted Net Loss Per Share | |||||||
Three Months Ended March 31, | |||||||
| 2024 | 2023 | ||||||
| GAAP net loss | $ | (21,612,455 | ) | $ | (11,938,417 | ) | |
| Adjustments: | |||||||
| Stock-based compensation | |||||||
| Research and development(1) | 832,180 | 654,471 | |||||
| General and administrative(2) | 499,166 | 618,811 | |||||
| Non-cash interest expense(3) | 530,819 | 495,188 | |||||
| Non-cash interest income(4) | (153,845 | ) | (1,697,811 | ) | |||
| Non-GAAP adjusted net loss | $ | (19,904,135 | ) | $ | (11,867,758 | ) | |
| GAAP net loss per share - basic and diluted | $ | (0.64 | ) | $ | (0.55 | ) | |
| Adjustment to net loss (as detailed above) | 0.05 | 0.00 | |||||
| Non-GAAP adjusted net loss per share | $ | (0.59 | ) | $ | (0.55 | ) | |
| Weighted average common shares outstanding, basic and diluted | 33,612,054 | 21,680,877 | |||||
| (1) To reflect a non-cash charge to operating expense for Research and Development stock-based compensation. |
| (2) To reflect a non-cash charge to operating expense for General and Administrative stock-based compensation. |
| (3) To reflect a non-cash charge to other expense for amortization of debt issuance and discount costs |
| and PIK interest related to the issuance of a note payable. |
| (4) To reflect a non-cash adjustment to other income for accretion on investments. |
FAQ
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