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HURA Overview

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Intellectia

Loading chart...

High
2.850
Open
2.830
VWAP
2.72
Vol
1.12M
Mkt Cap
176.75M
Low
2.545
Amount
3.06M
EV/EBITDA(TTM)
--
Total Shares
63.58M
EV
176.78M
EV/OCF(TTM)
--
P/S(TTM)
--
TuHURA Biosciences, Inc. is a Phase III registration-stage immuno-oncology company developing novel technologies to overcome resistance to cancer immunotherapy. Its lead innate immune agonist, IFx-2.0, is designed to overcome primary resistance to checkpoint inhibitors. It has initiated a single randomized placebo-controlled Phase III registration trial of IFx-2.0 administered as an adjunctive therapy to Keytruda (pembrolizumab) compared to Keytruda plus placebo in first-line treatment for advanced or metastatic Merkel Cell Carcinoma. It is leveraging its Delta Opioid Receptor technology to develop bi-specific antibody drug conjugates and antibody peptide conjugates targeting Myeloid Derived Suppressor Cells to inhibit their immune-suppressing effects on the tumor microenvironment to prevent T cell exhaustion and acquired resistance to checkpoint inhibitors and cellular therapies. It is also focused on the novel VISTA inhibiting mAb, known as TBS-2025.
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Events Timeline

(ET)
2026-02-17
07:50:00
TuHURA Biosciences Files INDA for TBS-2025 with FDA
select
2026-02-02 (ET)
2026-02-02
07:50:00
TuHURA Biosciences IFx-2.0 Receives Orphan Drug Designation
select
2025-12-15 (ET)
2025-12-15
08:10:00
TuHURA Biosciences Announces Kintara REM-001 Clinical Trial Success
select
2025-12-11 (ET)
2025-12-11
07:40:00
TuHURA Biosciences Secures $15.6 Million Financing to Advance AML Research
select
2025-12-09 (ET)
2025-12-09
10:00:00
TuHURA Biosciences Issues 9,462,423 Shares at $1.65 Each
select
2025-12-08 (ET)
2025-12-08
08:00:00
TuHURA Biosciences Presents DOR Research Findings at ASH Annual Meeting
select
2025-07-01 (ET)
2025-07-01
08:53:46
TuHURA Biosciences included in Russell 3000 and 2000 Indexes
select

News

PRnewswire
5.0
04-07PRnewswire
TuHURA Appoints New SVP of Clinical Operations
  • New Executive Appointment: TuHURA Biosciences has appointed Amanda Garofalo as Senior Vice President of Clinical Operations, bringing over 20 years of drug development experience, which is expected to enhance the efficiency of the company's clinical programs.
  • Advancing Clinical Programs: Garofalo will closely collaborate with CEO James Bianco and Dr. Craig Tendler to drive the Phase 3 accelerated approval trial of IFx-2.0 and the Phase 1b/2 trial of TBS-2025, aiding the company in achieving its clinical milestones.
  • Rich Industry Background: Prior to joining TuHURA, Garofalo was instrumental in executing a $305 million Series F funding round at Parabilis Medicines, showcasing her exceptional capabilities in clinical trial and data management, which is anticipated to optimize TuHURA's resource utilization.
  • Diverse Professional Experience: Garofalo managed over 200 oncology clinical trials at EMD Serono and successfully directed multiple new IND submissions, demonstrating her extensive experience across all stages of drug development, which will provide robust support for TuHURA's R&D strategy.
seekingalpha
9.5
04-01seekingalpha
TuHURA Biosciences Reports FY Net Loss of $30.05 Million
  • Annual Financial Performance: TuHURA Biosciences reported a net loss of $30.05 million for the fiscal year, indicating significant pressure in market competition and challenges in profitability, which could impact future financing and investor confidence.
  • Financial Data Analysis: Despite the losses, the company's financial information suggests that TuHURA is actively seeking to improve operational efficiency and cost control, aiming for profitability in the future to enhance its competitive position in the market.
  • Market Reaction: Investors have reacted lukewarmly to TuHURA's financial performance, which may lead to downward pressure on stock prices, further affecting the company's capital-raising capabilities and market positioning.
  • Future Outlook: The company needs to develop effective strategies to address current financial challenges, particularly in R&D and marketing, to maintain competitiveness and achieve sustainable growth in the biotechnology sector.
PRnewswire
9.5
04-01PRnewswire
TuHURA Biosciences Reports Strong 2025 Financial Results and Strategic Developments
  • Strong Financial Performance: TuHURA Biosciences reported cash and cash equivalents of $3.6 million for 2025, with an additional $7.5 million raised in Q1 2026 through a registered direct offering, enhancing financial flexibility to support ongoing R&D efforts.
  • Increased R&D Spending: Research and development expenses rose to $20.5 million in 2025 from $13.3 million in 2024, reflecting the company's commitment to advancing its clinical development and novel therapeutics in immuno-oncology, aiming to accelerate project timelines.
  • Clinical Trial Progress: The Phase 3 study of IFx-2.0 is currently enrolling, with completion anticipated by mid-2027, which will significantly bolster the company's competitive edge in the cancer immunotherapy market.
  • Enhanced Strategic Leadership: The appointment of Dr. Craig Tendler to oversee clinical development strategy and operations aims to leverage his extensive experience to advance the VISTA inhibiting antibody TBS-2025, thereby strengthening the company's R&D capabilities and market positioning.
PRnewswire
5.0
03-23PRnewswire
TuHURA Biosciences Appoints New CMO to Drive Oncology Strategy
  • Executive Appointment: TuHURA Biosciences has appointed Dr. Craig L. Tendler as Chief Medical Officer (CMO), who will oversee clinical development strategy and operations, leveraging his 30 years of experience in oncology to advance the TBS-2025 program, which is expected to significantly enhance the company's competitiveness in blood-related cancer treatments.
  • Regulatory Approval Achievements: Dr. Tendler has coordinated over 30 regulatory approvals and 15 new medical entity approvals in oncology, including four biologic or cell therapy approvals, generating over $16 billion in global sales, highlighting his substantial impact in the industry.
  • Clinical Development Plans: TuHURA's TBS-2025 project has received preliminary feedback from the FDA, and Dr. Tendler will utilize his extensive experience in NPM1 mutated acute myeloid leukemia (AML) to accelerate the clinical development of this drug, aiming to improve overall survival rates for patients.
  • Strategic Collaboration and Investment: Dr. Tendler's successful tenure at Johnson & Johnson, including collaborations with the FDA and EMA to secure global approvals for transformative therapies, will provide invaluable strategic guidance for TuHURA's future development, particularly in the complex landscape of oncology drug development.
PRnewswire
8.5
02-27PRnewswire
TuHURA Biosciences Regains Nasdaq Compliance
  • Compliance Regained: TuHURA Biosciences announced on February 26, 2026, that it has regained compliance with Nasdaq's listing standards, with its stock closing above $1.00 for the last 11 consecutive trading days, enhancing the company's market stability and investor confidence.
  • Clinical Trial Progress: The company is advancing its Phase 3 accelerated approval trial for IFX-2.0 targeting front-line Merkel Cell Carcinoma, demonstrating its ongoing innovation in the cancer immunotherapy sector.
  • New Drug Development: TuHURA is preparing for the initiation of a Phase 2 study for TBS-2025, a VISTA inhibiting antibody aimed at treating relapsed/refractory NPM1 mutated AML, further enriching its product pipeline.
  • Technological Innovation: The company is also developing first-in-class bi-specific antibody drug conjugates leveraging Delta Opioid Receptor technology to inhibit immune-suppressing effects in the tumor microenvironment, thereby enhancing the efficacy of immunotherapy.
Newsfilter
8.5
02-27Newsfilter
TuHURA Biosciences Regains Nasdaq Compliance
  • Compliance Regained: TuHURA Biosciences announced on February 26, 2026, that it has regained compliance with Nasdaq's minimum bid price requirement of $1.00, as the company's stock price remained above this threshold for 11 consecutive business days, thereby alleviating compliance concerns and boosting investor confidence.
  • Clinical Trial Progress: The company is advancing its Phase 3 accelerated approval trial for IFX-2.0 in front-line Merkel Cell Carcinoma, indicating ongoing commitment to cancer immunotherapy and potential market opportunities.
  • New Drug Development: TuHURA is preparing to initiate a Phase 2 study for TBS-2025 targeting relapsed/refractory NPM1 mutated AML, further diversifying its product pipeline and enhancing competitive positioning in the oncology market.
  • Technological Innovation: The company is developing first-in-class bi-specific antibody drug conjugates aimed at inhibiting immune-suppressing cells in the tumor microenvironment to prevent T cell exhaustion and acquired resistance, showcasing its innovative potential in immuno-oncology.
Wall Street analysts forecast HURA stock price to rise
2 Analyst Rating
Wall Street analysts forecast HURA stock price to rise
2 Buy
0 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
8.00
Averages
9.00
High
10.00
Current: 0.000
sliders
Low
8.00
Averages
9.00
High
10.00
Rodman & Renshaw
Buy
initiated
$7
AI Analysis
2026-04-15
Reason
Rodman & Renshaw
Price Target
$7
AI Analysis
2026-04-15
initiated
Buy
Reason
Rodman & Renshaw initiated coverage of TuHURA Biosciences with a Buy rating and $7 price target. The firm's target is based on its estimate of the probability-adjusted sum-of-the-parts valuation of three distinct immuno-oncology technologies being investigated by TuHURA, the analyst tells investors.
H.C. Wainwright
Robert Burns
Buy
downgrade
$12 -> $10
2026-01-09
Reason
H.C. Wainwright
Robert Burns
Price Target
$12 -> $10
2026-01-09
downgrade
Buy
Reason
H.C. Wainwright analyst Robert Burns lowered the firm's price target on TuHURA Biosciences to $10 from $12 and keeps a Buy rating on the shares. The firm says the company's "upcoming value inflection points and recent stock decline provide an attractive entry point."
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for HURA
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Valuation Metrics

The current forward P/E ratio for TuHURA Biosciences Inc (HURA.O) is 0.00, compared to its 5-year average forward P/E of -6.67. For a more detailed relative valuation and DCF analysis to assess TuHURA Biosciences Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-6.67
Current PE
0.00
Overvalued PE
-3.19
Undervalued PE
-10.16

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
0.00
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
0.00
Undervalued EV/EBITDA
0.00

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PS
2.00
Current PS
8.23
Overvalued PS
6.49
Undervalued PS
-2.49

Financials

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Frequently Asked Questions

What is TuHURA Biosciences Inc (HURA) stock price today?

The current price of HURA is 2.78 USD — it has decreased -1.77

What is TuHURA Biosciences Inc (HURA)'s business?

TuHURA Biosciences, Inc. is a Phase III registration-stage immuno-oncology company developing novel technologies to overcome resistance to cancer immunotherapy. Its lead innate immune agonist, IFx-2.0, is designed to overcome primary resistance to checkpoint inhibitors. It has initiated a single randomized placebo-controlled Phase III registration trial of IFx-2.0 administered as an adjunctive therapy to Keytruda (pembrolizumab) compared to Keytruda plus placebo in first-line treatment for advanced or metastatic Merkel Cell Carcinoma. It is leveraging its Delta Opioid Receptor technology to develop bi-specific antibody drug conjugates and antibody peptide conjugates targeting Myeloid Derived Suppressor Cells to inhibit their immune-suppressing effects on the tumor microenvironment to prevent T cell exhaustion and acquired resistance to checkpoint inhibitors and cellular therapies. It is also focused on the novel VISTA inhibiting mAb, known as TBS-2025.

What is the price predicton of HURA Stock?

Wall Street analysts forecast HURA stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for HURA is9.00 USD with a low forecast of 8.00 USD and a high forecast of 10.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is TuHURA Biosciences Inc (HURA)'s revenue for the last quarter?

TuHURA Biosciences Inc revenue for the last quarter amounts to -4.49M USD, decreased -70.79

What is TuHURA Biosciences Inc (HURA)'s earnings per share (EPS) for the last quarter?

TuHURA Biosciences Inc. EPS for the last quarter amounts to -5583872.00 USD, decreased -56.70

How many employees does TuHURA Biosciences Inc (HURA). have?

TuHURA Biosciences Inc (HURA) has 22 emplpoyees as of April 22 2026.

What is TuHURA Biosciences Inc (HURA) market cap?

Today HURA has the market capitalization of 176.75M USD.