GBAF Logo
Global Banking & Finance Awards® 2026 Nominations open, free to enter Nominate now →
T

TuHURA Biosciences HURA · USD

Health Care · US listing · 🇺🇸 United States

Compare

1.66

+1.84%

Close of 9 Nov 2026, in USD

Search any instrument

Reference data, closing prices and charts across 45,000 companies, plus crypto, commodities and currencies.

About TuHURA Biosciences

From its filings with the US Securities and Exchange Commission

SEC filings

TuHURA Biosciences is based in Tampa, Florida and is incorporated in Nevada. Its shares trade on Nasdaq under the ticker HURA. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported revenue of $0 and a net loss of $30.1m. At that date it held total assets of $27.4m and shareholders' equity of $20.9m.

In its own words

We are a phase 3 clinical stage immuno-oncology company with three distinct technologies focused on the development of novel therapeutics designed to overcome primary and acquired resistance to cancer immunotherapies.

Our proprietary Immune FxTM technology platform, or IFx, is an innate immune agonist technology designed to “trick” the body’s immune system to attack tumor cells by making tumor cells look like bacteria. Our lead product candidate, IFx2.0, is an innate immune agonist designed to overcome primary resistance to checkpoint inhibitors. In June 2025, we initiated a single randomized placebo-controlled Phase 3 registration trial of administered as an adjunctive therapy to Keytruda® (pembrolizumab) in first line treatment for patients with advanced or metastatic Merkel cell carcinoma who are checkpoint inhibitor naïve utilizing the FDA’s accelerated approval pathway.

In addition to our IFx technology platform, in June 2025 we acquired the rights to TBS-2025, a novel VISTA-inhibiting monoclonal antibody formerly known as KVA1213, through our acquisition of Kineta, Inc. (“Kineta”) on June 30, 2025. VISTA (otherwise referred to as V-domain Ig suppressor of T cell activation) is an immune checkpoint highly expressed on myeloid cells that is believed to be a strong driver of immunosuppression in the tumor microenvironment and is believed to be a primary mechanism by which leukemic blasts escape immune recognition contributing to low response rates and high rates of recurrence in acute myeloid leukemia, or AML.

Quoted from its 10-K, filed 31 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
12 Jul 2016
Employees
22
Website
kintara.com ↗
Head office
10500 UNIVERSITY CENTER DR., TAMPA, FL, 33612
Incorporated in
NV
Classification
Pharmaceutical Preparations
Filer status
Non-accelerated filer<br>Smaller reporting company

Leadership

Pay as last reported

  • Dr. James ManusoIndependent Chairman of the Board$14,750
  • Dr. James BiancoChief Executive Officer, Director, since 2024$5.4m
  • Mr. Dan DearbornChief Financial Officer$2.5m
  • Mr. Robert HoffmanDirector, since 2018$2.5m
  • Dr. Alan ListIndependent Director$13,875
  • Mr. George NgIndependent Director$14,125
  • Dr. Craig TendlerIndependent Director
  • Ms. Jenene ThomasInvestor Relations, since 2025

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
0
Environment
0
Social
0
Governance
0

SWOT analysis

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

AI-generated

Strengths

  • Kintara Therapeutics focuses on cancer therapies with VAL-083 in Phase II trials for glioblastoma multiforme.
  • VAL-083 has over 40 clinical trials sponsored by the National Cancer Institute.
  • Kintara holds commercial rights for VAL-083 in China for CML and lung cancer treatment.

Weaknesses

  • Kintara employs only 4 full-time employees in San Diego, California.
  • The company's IPO occurred on 12 July 2016, indicating limited market presence.
  • VAL-083 is only in Phase II clinical trials for GBM without approved treatments.

Opportunities

  • VAL-083 could expand to treat ovarian cancer and NSCLC beyond GBM.
  • Kintara may leverage NCI-sponsored trials for additional cancer indications.
  • Commercial rights in China for CML and lung cancer present growth potential.

Threats

  • VAL-083 faces competition from existing cancer therapies in the US market.
  • Clinical trial delays could impact the development timeline for VAL-083.
  • Regulatory changes in China might affect commercial rights for VAL-083.

Sources and methodology

Data on this tab
Our data supplier
Chart on the Overview
TradingView

Nothing here is investment advice. Prices can be delayed or wrong, so check with the exchange before relying on them. Data for this page. How we cover markets.