Full Press Release Details
Third Quarter 2023 Financial Results and Provides Business Update
Alignment with the FDA on the Data Package Requirements to File NDA for
oxylanthanum carbonate (OLC)
Pivotal Clinical Trial Expected to Initiate Before Year End
LOS ALTOS, Calif., November
14, 2023 -- Unicycive Therapeutics, Inc. (Nasdaq: UNCY) (the "Company" or "Unicycive"),
a clinical-stage biotechnology company developing therapies for patients with kidney disease, today announced its financial results
for the third quarter ended September 30, 2023, and provided a business update.
with the FDA on our clinical development plan for oxylanthanum carbonate (OLC) was a major achievement as we are one step closer to potentially
bringing a much-needed therapy to individuals living with chronic kidney disease on dialysis," said Shalabh Gupta, M.D., Chief Executive
Officer of Unicycive. "With clear visibility on the path forward to file an NDA, we expect to initiate the pivotal clinical trial
before the end of this year. Topline data is expected in mid-2024, and we plan to finalize the NDA package and submit to the FDA shortly
"In addition, last quarter we were excited
to welcome Dr. Sara Kenkare-Mitra to our Board of Directors, adding a seasoned executive with decades of drug development and corporate
leadership experience. We also remain very active within the the medical community with a booth at Kidney Week and positive results published
on the phosphate binding capacity for OLC," concluded Dr. Gupta.
for the Third Quarter Ended September 30, 2023
Licensing Revenues: Licensing
revenues were $0 compared to $1.0 million for the same period in 2022, due to an upfront payment for a licensing agreement entered into
with Lee's Pharmaceutical (HK) Limited in July 2022.
Research and Development
(R&D) Expenses: R&D expenses were $3.4 million, compared to $4.8 million for the same period in 2022. A decrease in drug development
costs of approximately $1.9 million was due to completion of significant preclinical development work in the prior period. The decrease
in development costs was partially offset by increases in labor costs of $0.1 million and non-cash stock compensation costs of $0.3 million.
General and Administrative
(G&A) Expenses: G&A expenses were $2.6 million, compared to $1.7 million for the same period in 2022. This increase was primarily
due to an increase of $0.4 million in consulting and professional services costs. Stock compensation costs increased $0.3 million from
the prior period. Labor, travel, rent, and other costs increased $0.3 million, and insurance expenses for directors and officers decreased
Other Income (Expenses):
Other income (expenses) increased $1.6 million due primarily to the change in fair value of our warrant liability.
Net Loss: Net loss attributable
to common stockholders was $4.4 million, or $0.13 per share of common stock, compared to a net loss of $5.6 million, or $0.37 per share
of common stock, for the same three-month period in 2022. This decrease was attributable primarily to a $1.4 million change in fair value
of our warrant liability.
Cash Position: As of September 30, 2023, cash and cash equivalents
totaled $14.3 million which is expected to last into the second half of 2024 including completion of the pivotal clinical trial and topline
Oxylanthanum carbonate
is a next-generation lanthanum-based phosphate binding agent utilizing proprietary nanoparticle technology being developed for the treatment
of hyperphosphatemia in patients with chronic kidney disease (CKD). OLC has over forty issued and granted patents globally. Its potential
best-in-class profile may have meaningful patient adherence benefits over currently available treatment options as it requires a lower
pill burden for patients in terms of number and size of pills per dose that are swallowed instead of chewed. Based on a survey conducted
in 2022, Nephrologists stated that the greatest unmet need in the treatment of hyperphosphatemia with phosphate binders is a lower pill
burden and better patient compliance.1 The global market opportunity for treating hyperphosphatemia is projected to be
in excess of $2.5 billion in 2023, with the United States accounting for more than $1 billion of that total. Despite the availability
of several FDA-cleared medications, 75 percent of U.S. dialysis patients fail to achieve the target phosphorus levels recommended by published
Unicycive is seeking
FDA approval of OLC via the 505(b)(2) regulatory pathway. As part of the clinical development program, two clinical studies were conducted
in over 100 healthy volunteers. The first study was a dose-ranging Phase I study to determine safety and tolerability. The second study
was a randomized, open-label, two-way crossover bioequivalence study to establish pharmacodynamic bioequivalence between OLC and Fosrenol.
Based on the topline results of the bioequivalence study, pharmacodynamic (PD) bioequivalence of OLC to Fosrenol was established.
Fosrenol is a registered trademark
of Shire International Licensing BV.
About Unicycive Therapeutics
Unicycive Therapeutics is a biotechnology company
developing novel treatments for kidney diseases. Unicycive's lead drug candidate, oxylanthanum carbonate (OLC), is a novel investigational
phosphate binding agent being developed for the treatment of hyperphosphatemia in chronic kidney disease patients on dialysis. UNI-494
is a patent-protected new chemical entity in late preclinical development for the treatment of acute kidney injury. For more information,
please visit Unicycive.com.
Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform
Act of 1995. These statements may be identified using words such as "anticipate," "believe," "forecast,"
"estimated" and "intend" or other similar terms or expressions that concern Unicycive's expectations, strategy,
plans or intentions. These forward-looking statements are based on Unicycive's current expectations and actual results could differ
materially. There are several factors that could cause actual events to differ materially from those indicated by such forward-looking
statements. These factors include, but are not limited to, clinical trials involve a lengthy and expensive process with an uncertain
outcome, and results of earlier studies and trials may not be predictive of future trial results; our clinical trials may be suspended
or discontinued due to unexpected side effects or other safety risks that could preclude approval of our product candidates; risks related
to business interruptions which could seriously harm our financial condition and increase our costs and expenses; dependence on key personnel;
substantial competition; uncertainties of patent protection and litigation; dependence upon third parties; and risks related to failure
to obtain FDA clearances or approvals and noncompliance with FDA regulations. Actual results may differ materially from those indicated
by such forward-looking statements as a result of various important factors, including: the uncertainties related to market conditions
and other factors described more fully in the section entitled Risk Factors' in Unicycive's Annual Report on Form
10-K for the year ended December 31, 2022, and other periodic reports filed with the Securities and Exchange Commission. Any forward-looking
statements contained in this press release speak only as of the date hereof, and Unicycive specifically disclaims any obligation to update
any forward-looking statement, whether as a result of new information, future events or otherwise.
SOURCE: Unicycive Therapeutics, Inc.
--Tables to Follow--
Unicycive Therapeutics, Inc.
(in thousands, except for share and
| As of | As of | |||||||
| December 31, | September 30, | |||||||
| 2022 | 2023 | |||||||
| (Unaudited) | ||||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash | $ | 455 | $ | 14,345 | ||||
| Prepaid expenses and other current assets | 2,189 | 4,224 | ||||||
| Total current assets | 2,644 | 18,569 | ||||||
| Right of use asset, net | 152 | 845 | ||||||
| Property, plant and equipment, net | 22 | 28 | ||||||
| Total assets | $ | 2,818 | $ | 19,442 | ||||
| Liabilities and stockholders' (deficit) equity | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 892 | $ | 1,084 | ||||
| Accrued liabilities | 2,237 | 2,530 | ||||||
| Warrant liability | - | 11,528 | ||||||
| Operating lease liability - current | 155 | 314 | ||||||
| Total current liabilities | 3,284 | 15,456 | ||||||
| Operating lease liability - long term | - | 552 | ||||||
| Total liabilities | 3,284 | 16,008 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders' (deficit) equity: | ||||||||
| Series A-2 preferred stock, $0.001 par value per share - zero and 43,649 shares authorized at December 31, 2022 and September 30, 2023, respectively; zero and 43,649 shares outstanding at December 31, 2022 and September 30, 2023, respectively | - | 44 | ||||||
| Preferred stock, $0.001 par value per share - 10,000,000 and 9,926,161 shares authorized at December 31, 2022 and September 30, 2023, respectively; zero shares issued and outstanding at December 31, 2022, and September 30, 2023 | - | - | ||||||
| Common stock, $0.001 par value per share - 200,000,000 shares authorized at December 31, 2022 and September 30, 2023; 15,231,655 shares issued and outstanding at December 31, 2022, and 34,754,401 shares issued and outstanding at September 30, 2023 | 15 | 35 | ||||||
| Additional paid-in capital | 33,516 | 60,098 | ||||||
| Accumulated deficit | (33,997 | ) | (56,743 | ) | ||||
| Total stockholders' (deficit) equity | (466 | ) | 3,390 | |||||
| Total liabilities and stockholders' (deficit) equity | $ | 2,818 | $ | 19,442 |
Unicycive Therapeutics, Inc.
Statements of Operations
(in thousands, except for share and
| Three Months Ended September 30, 2022 | Three Months Ended September 30, 2023 | |||||||
| Licensing revenues: | $ | 951 | $ | - | ||||
| Operating expenses: | ||||||||
| Research and development | 4,803 | 3,372 | ||||||
| General and administrative | 1,702 | 2,566 | ||||||
| Total operating expenses | 6,505 | 5,938 | ||||||
| Loss from operations | (5,554 | ) | (5,938 | ) | ||||
| Other income (expenses): | ||||||||
| Interest income | - | 227 | ||||||
| Interest expense | (3 | ) | (18 | ) | ||||
| Change in fair value of warrant liability | - | 1,396 | ||||||
| Total other income (expenses) | (3 | ) | 1,605 | |||||
| Net loss | (5,557 | ) | (4,333 | ) | ||||
| Deemed dividend to Series A-1 preferred stockholders | - | (72 | ) | |||||
| Net loss attributable to common stockholders | $ | (5,557 | ) | $ | (4,405 | ) | ||
| Net loss per share attributable to common stockholders, basic and diluted | $ | (0.37 | ) | $ | (0.13 | ) | ||
| Weighted-average shares outstanding used in computing net loss per share, basic and diluted | 15,061,995 | 32,633,074 |