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Unicycive Therapeutics to Present at the H.C. Wainwright 28th Annual Global Investment Conference

Unicycive Therapeutics (Nasdaq: UNCY) announced that CEO Shalabh Gupta, M.D., will present at the H.C.

(Neutral)

Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

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Unicycive Therapeutics (Nasdaq: UNCY) announced that CEO Shalabh Gupta, M.D., will present at the H.C. Wainwright 28th Annual Global Investment Conference on Tuesday, September 15, 2026, at 11 a.m. ET. A live and archived webcast will be available via the Investors section of the Unicycive website.

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Argus Sep 1 session 1 alert
-2.88% close to close 1.7x rel. volume Open Argus
Details

News Market Reaction – UNCY

$149.03M Market Cap

On Sep 1, the day this news came out, UNCY closed 2.88% below the previous close. Relative volume reached 1.7x the daily average during tracking.

Data tracked by StockTitan Argus for the Sep 1 session.

Key Figures

Conference date: September 15, 2026 Presentation time: 11 a.m. ET Trial phase: Phase 1
Conference date
September 15, 2026
H.C. Wainwright 28th Annual Global Investment Conference
Presentation time
11 a.m. ET
September 15, 2026 conference presentation
Trial phase
Phase 1
UNI-494 dose-ranging safety study in healthy volunteers

Historical Context

5 past events · Latest: Aug 12
5 events
  1. Aug 12

    Q2 earnings update

    24h Move
    +8.2%

    FDA complete response letter cited manufacturing deficiencies without new efficacy or safety concerns

  2. Jun 30

    FDA regulatory action

    24h Move
    -39.1%

    FDA issued another complete response letter citing previously identified manufacturing deficiencies

  3. May 12

    Q1 earnings update

    24h Move
    +2.8%

    FDA review remained on track with a June 29 PDUFA target action date

  4. Apr 09

    Conference presentation

    24h Move
    +3.1%

    CEO presentation was scheduled for the Needham Virtual Healthcare Conference

  5. Mar 30

    Full-year earnings

    24h Move
    -4.4%

    NDA resubmission acceptance and potential third-quarter commercial launch were announced

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

hyperphosphatemia, orphan drug designation, delayed graft function, dose-ranging safety study
4 terms
hyperphosphatemia medical
"for the treatment of hyperphosphatemia in patients with chronic kidney disease"
An elevated level of phosphate in the blood, often caused by reduced kidney function or certain medications, that can harm bones, blood vessels and organs if untreated. Investors should care because prevalence, safety concerns and regulatory scrutiny around treatments or diagnostics for this condition can drive demand, affect clinical trial outcomes, influence healthcare spending and change a company’s revenue and risk profile—similar to how a common road hazard can change demand for safety products.
orphan drug designation regulatory
"It has been granted orphan drug designation (ODD) by the FDA"
Orphan drug designation is a special status given to medicines developed to treat rare diseases affecting only a small number of people. This status often provides benefits like faster approval processes and financial incentives, making it more attractive for companies to develop these drugs. For investors, it signals potential for exclusive market rights and reduced competition, which can impact the drug’s profitability.
delayed graft function medical
"for the prevention of Delayed Graft Function (DGF) in kidney transplant patients"
Delayed graft function is when a transplanted organ—most commonly a kidney—does not start working right away after surgery, usually identified by the need for dialysis within the first week or by very low urine output. It matters to investors because it is a common clinical outcome used to measure transplant success, influences short-term hospital costs, patient recovery time, and can affect longer-term graft survival and regulatory or trial results.
dose-ranging safety study medical
"has completed a Phase 1 dose-ranging safety study in healthy volunteers"
A dose-ranging safety study is an early-stage clinical trial that tests several different doses of an investigational drug to find how much can be given safely and what side effects appear at each level. It matters to investors because these studies shape later trial design and regulatory chances—like a thermostat test that finds safe temperature ranges before running a full-scale system, their results influence development cost, timeline, and risk.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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LOS ALTOS, Calif., Sept. 01, 2026 (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 Shalabh Gupta, M.D., Chief Executive Officer, will present at the H.C. Wainwright 28th Annual Global Investment Conference on Tuesday, September 15, 2026, at 11 a.m. ET.

A link to the live and archived webcast may be accessed on the Unicycive website under the Investors section: Events and Presentations.

About Unicycive Therapeutics

Unicycive Therapeutics is a biotechnology company developing novel treatments for kidney diseases. Unicycive’s lead investigational treatment is oxylanthanum carbonate, a novel phosphate binding agent for the treatment of hyperphosphatemia in patients with chronic kidney disease who are on dialysis. Unicycive’s second investigational treatment UNI-494 is intended for the treatment of conditions related to acute kidney injury. It has been granted orphan drug designation (ODD) by the FDA for the prevention of Delayed Graft Function (DGF) in kidney transplant patients and has completed a Phase 1 dose-ranging safety study in healthy volunteers. For more information, please visit Unicycive.com and follow us on LinkedIn and X.

Investor Contact:

Kevin Gardner
LifeSci Advisors
kgardner@lifesciadvisors.com

Media Contact:

Unicycive Therapeutics
media@unicycive.com

SOURCE: Unicycive Therapeutics, Inc.


FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

When will Unicycive Therapeutics (UNCY) present at the H.C. Wainwright 28th Annual Global Investment Conference in 2026?

Unicycive Therapeutics will present on Tuesday, September 15, 2026, at 11 a.m. ET. According to Unicycive, CEO Shalabh Gupta, M.D., will deliver the presentation as part of the H.C. Wainwright 28th Annual Global Investment Conference.

How can investors access the Unicycive Therapeutics (UNCY) webcast for the H.C. Wainwright 2026 conference presentation?

Investors can access the live and archived webcast through the Unicycive website’s Investors > Events and Presentations section. According to Unicycive, the link will provide both real-time viewing and later on-demand access for interested stakeholders.

What is Unicycive Therapeutics’ lead investigational treatment mentioned ahead of the September 15, 2026 UNCY presentation?

Unicycive’s lead investigational treatment is oxylanthanum carbonate, a novel phosphate-binding agent. According to Unicycive, it is being developed to treat hyperphosphatemia in chronic kidney disease patients who are on dialysis, targeting phosphate control in this population.

What is UNI-494 in Unicycive Therapeutics’ (UNCY) pipeline and what stage is it in?

UNI-494 is Unicycive’s second investigational treatment intended for conditions related to acute kidney injury. According to Unicycive, UNI-494 has FDA orphan drug designation for preventing delayed graft function and has completed a Phase 1 dose-ranging safety study in healthy volunteers.

Does UNI-494 from Unicycive Therapeutics (UNCY) have FDA orphan drug designation and for what indication?

Yes, UNI-494 has FDA orphan drug designation for preventing delayed graft function in kidney transplant patients. According to Unicycive, this investigational therapy targets complications related to acute kidney injury in the transplant setting.

What disease areas is Unicycive Therapeutics (UNCY) focused on as it presents at the 2026 H.C. Wainwright conference?

Unicycive focuses on developing novel treatments for kidney diseases, including chronic and acute conditions. According to Unicycive, its pipeline includes oxylanthanum carbonate for hyperphosphatemia in dialysis patients and UNI-494 for conditions related to acute kidney injury in transplant settings.

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