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Unicycive Therapeutics Announces Both an Oral and Poster Presentation to be Delivered on UNI-494 at the Upcoming AKI and CRRT Conference

Key Takeaway: Unicycive Therapeutics announced two presentations on UNI-494 at the upcoming AKI and CRRT 2024 conference. The presentations will cover the efficacy of UNI-494 in animal models of acute kidney injury and the design of its ongoing Phase 1 clinical trial. The company aims to build data on UNI-494 while focusing on its lead drug candidate, OLC.
Price reaction · baseline $8.749 (2024-01-26 close) · clean, no other UNCY news in the window
day 0 close
+7.4%
day 1
+6.3%
day 3 · peak
+9.7%

Market Sentiment Analysis

POSITIVE FACTORS

  • Unicycive is advancing its second clinical stage program, UNI-494.
  • Presentations at a major conference highlight the company's ongoing research.
  • UNI-494 has a novel mechanism that may restore mitochondrial function.

CONCERNS & RISKS

  • Clinical trials involve lengthy processes with uncertain outcomes.
  • Results from earlier studies may not predict future trial results.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+39%
120-day peak, hindsight
Typical move
26.6%
average across 4 past catalysts
Cash runway
~24 mo
Low dilution risk
Lead asset
Oxylanthanum Carbonate
Phase 2 · Chronic Kidney Disease Requiring Chronic Dialysis

Full Press Release Details

New Preclinical Data on UNI-494 in Acute Kidney Injury

LOS ALTOS, Calif., Jan. 29, 2024 (GLOBE NEWSWIRE) -- Unicycive Therapeutics, Inc. (Nasdaq: UNCY), a clinical-stage biotechnology company developing therapies for patients with kidney disease (the “Company or “Unicycive”), today announced that two presentations related to UNI-494 will be presented at the 29 th International Conference on Advances in Critical Care Nephrology AKI and CRRT 2024 taking place March 12-15, 2024, in San Diego, CA.
Shalabh Gupta, MD, Chief Executive Officer of Unicycive, commented, “We are looking forward to presenting data on the efficacy of our second clinical stage program UNI-494 in animal models of delayed graft function, a manifestation of acute kidney injury (AKI) that occurs during kidney transplantation resulting in loss of kidney function. We are also presenting a poster describing our ongoing Phase 1 clinical trial design for UNI-494 in healthy volunteers. Based on the results from this trial, we will determine the best path forward for the program. While our primary focus is on advancing our lead drug, OLC (Oxylanthanum Carbonate) towards a New Drug Application submission, we continue to build a body of data on UNI-494 as it progresses through its first clinical trial.”
About UNI-494
UNI-494 is a novel nicotinamide ester derivative and a selective ATP-sensitive mitochondrial potassium channel activator. Mitochondrial dysfunction plays a critical role in the progression of acute kidney injury and chronic kidney disease. UNI-494 has a novel mechanism of action that restores mitochondrial function and may be beneficial for the treatment of several diseases including kidney disease. Unicycive is currently conducting a Phase 1 dose-ranging safety study in healthy volunteers in the United Kingdom that is expected to complete this year. UNI-494 is protected by issued patent(s) in the U.S. and Europe and a wide range of patent applications worldwide.
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 and follow us on LinkedIn and YouTube .
Forward-looking statements
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.
Investor Contact:
ir@unicycive.com (650) 543-5470
SOURCE: Unicycive Therapeutics, Inc.
Released January 29, 2024

Frequently Asked Questions

What is UNI-494?

UNI-494 is a novel nicotinamide ester derivative aimed at treating acute kidney injury.

When will the AKI and CRRT 2024 conference take place?

The conference will be held from March 12-15, 2024, in San Diego, CA.

What will Unicycive present at the conference?

Unicycive will present data on UNI-494's efficacy and its Phase 1 clinical trial design.

What is the focus of the Phase 1 trial for UNI-494?

The Phase 1 trial focuses on the safety and efficacy of UNI-494 in healthy volunteers.

Last updated: Jan 29, 2024