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Talphera TLPH · USD

Health Care · US listing · 🇺🇸 United States

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1.09

+3.81%

Close of 9 Nov 2026, in USD

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About Talphera

From its filings with the US Securities and Exchange Commission

SEC filings

Talphera is based in San Mateo, California and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker TLPH. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported revenue of $28,000 and a net loss of $14.3m. At that date it held total assets of $29.7m and shareholders' equity of $17.0m.

In its own words

We are a specialty pharmaceutical company focused on the development and commercialization of innovative therapies for use in medically supervised settings.

Our portfolio is principally focused on our lead product candidate, Niyad (nafamostat mesylate), for use as a regional anticoagulant during continuous renal replacement therapy, or CRRT. In addition, we may develop LTX-608, a nafamostat formulation for direct IV infusion for one or more of the following indications: disseminated intravascular coagulation, or DIC, acute respiratory distress syndrome, or ARDS, acute pancreatitis, or as an anti-viral treatment. We have two pre-filled syringe product candidates that have been explored but are being evaluated for discontinuation.

Received an investigational device exemption, or IDE, and Breakthrough Device Designation from the United States Food and Drug Administration, or FDA, and registrational trial is ongoing with completion expected in 2026.

IND will be evaluated for submission following toxicology evaluation to enable Phase 2 study.

We are developing Niyad to become the first and only FDA-approved regional anticoagulant for use in adult patients undergoing CRRT. Niyad is infused into the extracorporeal circuit, such as the dialysis circuit during CRRT for acute kidney injury, or AKI, patients in the hospital. In the future, Niyad may have benefit for use in chronic kidney disease patients undergoing intermittent hemodialysis, or IHD, in dialysis centers. Our initial priority is for use during CRRT, which is the focus of the current registrational study.

Quoted from its 10-K, filed 23 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Pharmaceuticals
Listed since
11 Feb 2011
Employees
19
Website
acelrx.com ↗
Head office
1850 GATEWAY DRIVE, SAN MATEO, CA, 94404
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
Non-accelerated filer<br>Smaller reporting company

Leadership

Pay as last reported

  • Mr. Adrian AdamsIndependent Chairman of the Board$80,806
  • Mr. Vincent AngottiChief Executive Officer, Director, since 2017$1.0m
  • Mr. Raffi AsadorianChief Financial Officer$709,857
  • Dr. Shakil AslamChief Development Officer, Chief Medical Officer
  • Mr. Badri DasuChief Engineering Officer$575,959
  • Ms. Marina BozilenkoIndependent Director$62,283
  • Ms. Jill BroadfootIndependent Director$56,349
  • Dr. Stephen HoffmanIndependent Director$52,517
  • Mr. Abhinav JainIndependent Director$57,074
  • Mr. Mark WanIndependent Director$63,458

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
52
Environment
59
Social
33
Governance
65
Carbon reduction policy
No
Human rights policy
No

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • AcelRx Pharmaceuticals develops Niyad for acute kidney injury in hospital settings.
  • Niyad targets dialysis circuits during CRRT for AKI patients in hospitals.
  • LTX-608 is formulated for IV infusion to treat COVID and ARDS.

Weaknesses

  • AcelRx employs only 19 full-time employees in San Mateo.
  • The company has no products approved for commercial use yet.
  • Niyad and LTX-608 are still in development stages.

Opportunities

  • Niyad addresses the growing need for anticoagulants in dialysis centers.
  • LTX-608 could expand to treat ARDS and DIC in hospitals.
  • The firm's pre-filled syringes Fedsyra and PFS-02 may enter new markets.

Threats

  • Niyad faces competition from existing anticoagulant therapies.
  • LTX-608 development could be delayed by regulatory hurdles.
  • The small team of 19 employees may struggle with scaling production.

Sources and methodology

Data on this tab
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