TuHURA Biosciences Announces Kintara REM-001 Clinical Trial Success
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Dec 15 2025
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Should l Buy HURA?
TuHURA Biosciences announced that Kintara's REM-001 clinical trial of ten metastatic cutaneous breast cancer patients met its primary endpoint demonstrating safety with signs of clinical efficacy following eight weeks of follow-up for such patients. Pursuant to the terms of the Contingent Value Rights Agreement dated as of October 18, 2024, by and between TuHURA Biosciences, Inc. and the rights agent, Equiniti Trust Company, as a result of the trial and the completion of the follow-up, the milestone required for the release of an aggregate of 1,539,958 shares of TuHURA common stock to legacy Kintara Therapeutics stockholders has been achieved. The holders of CVRs are entitled to receive shares of TuHURA common stock, subject to the terms of the CVR Agreement and any applicable withholding.
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Analyst Views on HURA
Wall Street analysts forecast HURA stock price to rise
2 Analyst Rating
2 Buy
0 Hold
0 Sell
Moderate Buy
Current: 1.790
Low
8.00
Averages
9.00
High
10.00
Current: 1.790
Low
8.00
Averages
9.00
High
10.00
About HURA
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.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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.
See More
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.
See More
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.
See More
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.
See More
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.
See More
TuHURA Biosciences to Participate in Upcoming Investor Conferences
- Investor Conference Schedule: TuHURA's CEO, James Bianco, will participate in the Citizens Life Science Conference on March 10, 2026, where he will present online, likely increasing investor interest and enhancing the company's visibility.
- One-on-One Investor Meetings: At the Leerink Global Healthcare Conference on March 11, 2026, TuHURA will offer one-on-one meetings with investors, which will help strengthen relationships with potential investors and drive funding opportunities.
- Clinical Trial Progress: TuHURA is conducting a Phase 3 registration trial for IFx-2.0 as an adjunct therapy to Keytruda, aimed at overcoming primary resistance to cancer immunotherapy, which, if successful, will significantly enhance the company's competitive position in the oncology market.
- Technological Innovation and Acquisition: TuHURA acquired TBS-2025 through its merger with Kineta Inc., which is moving into Phase 2 development, showcasing the company's innovative capabilities and potential for market expansion in immuno-oncology.
See More
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.
See More
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.
See More
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.
See More
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.
See More
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.
See More
TuHURA Biosciences to Participate in Upcoming Investor Conferences
- Investor Conference Schedule: TuHURA's CEO, James Bianco, will participate in the Citizens Life Science Conference on March 10, 2026, where he will present online, likely increasing investor interest and enhancing the company's visibility.
- One-on-One Investor Meetings: At the Leerink Global Healthcare Conference on March 11, 2026, TuHURA will offer one-on-one meetings with investors, which will help strengthen relationships with potential investors and drive funding opportunities.
- Clinical Trial Progress: TuHURA is conducting a Phase 3 registration trial for IFx-2.0 as an adjunct therapy to Keytruda, aimed at overcoming primary resistance to cancer immunotherapy, which, if successful, will significantly enhance the company's competitive position in the oncology market.
- Technological Innovation and Acquisition: TuHURA acquired TBS-2025 through its merger with Kineta Inc., which is moving into Phase 2 development, showcasing the company's innovative capabilities and potential for market expansion in immuno-oncology.
See More
