Maxim Group Continues to Recommend Buy for TuHURA Biosciences (HURA)
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Nov 15 2025
0mins
Should l Buy HURA?
Source: NASDAQ.COM
Analyst Recommendation: Maxim Group has maintained a Buy recommendation for TuHURA Biosciences, with a projected one-year price target of $11.54/share, indicating a potential upside of 458.78% from its current price of $2.06/share.
Fund Sentiment: There has been a significant increase in institutional interest in TuHURA Biosciences, with 119 funds reporting positions, marking an 83.08% increase in ownership over the last quarter.
Shareholder Activity: Notable shareholders include Vanguard Total Stock Market Index Fund, which increased its holdings by 15.22%, and Geode Capital Management, which also increased its shares but reduced its portfolio allocation by 42.57%.
Fintel Overview: Fintel provides comprehensive investing research, including fundamentals, analyst reports, and fund sentiment, aimed at individual investors and small hedge funds.
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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: 1.730
Low
8.00
Averages
9.00
High
10.00
Current: 1.730
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 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 to Participate in Upcoming Investor Conferences
- Investor Conference Schedule: TuHURA Biosciences CEO James Bianco will participate in the Citizens Life Science Conference on March 10, 2026, and the Leerink Global Healthcare Conference on March 11, showcasing the company's advancements in cancer immunotherapy, which is expected to attract potential investors' interest.
- Clinical Trial Progress: TuHURA is conducting a Phase 3 registration trial for IFx-2.0, designed to be used in conjunction with Keytruda® for advanced or metastatic Merkel Cell Carcinoma, and if successful, it will significantly enhance the company's competitiveness in the cancer treatment market.
- Technological Innovation: The company is advancing TBS-2025, an antibody drug targeting mutNPM1 relapsed/refractory acute myeloid leukemia, into Phase 2 development, which, if successful, will further enrich TuHURA's product pipeline and strengthen its market position.
- Strategic Acquisition: TuHURA's merger with Kineta Inc. has brought TBS-2025 into its portfolio, demonstrating its expansion strategy in cancer immunotherapy aimed at addressing primary and acquired resistance issues in cancer treatments.
See More
TuHURA Files IND for TBS-2025 in AML Treatment
- New Drug Application: TuHURA Biosciences has filed an Investigational New Drug (IND) application with the FDA for TBS-2025, aimed at treating mutNPM1 relapsed/refractory Acute Myeloid Leukemia (AML) in combination with a menin inhibitor, potentially improving patient response rates.
- Clinical Trial Design: The company plans to initiate a Phase 2 clinical trial in menin inhibitor-naïve patients in early Q2 2026, utilizing a Simon 2 stage design, with preliminary results expected in Q3 2026, demonstrating ongoing commitment to this therapeutic area.
- Scientific Rationale: Research indicates that mutations like mutNPM1 may drive VISTA expression on leukemic cells, leading to poor treatment responses; TuHURA believes that adding TBS-2025 could significantly enhance both the CR/CRh rates and their duration, addressing unmet medical needs.
- Safety Assessment: TBS-2025 has shown a favorable safety profile in early trials at a maximum dose of 1,000mg every two weeks, with the optimal Phase 2 dose projected at 750mg every three weeks, laying a solid foundation for further clinical development.
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 to Participate in Upcoming Investor Conferences
- Investor Conference Schedule: TuHURA Biosciences CEO James Bianco will participate in the Citizens Life Science Conference on March 10, 2026, and the Leerink Global Healthcare Conference on March 11, showcasing the company's advancements in cancer immunotherapy, which is expected to attract potential investors' interest.
- Clinical Trial Progress: TuHURA is conducting a Phase 3 registration trial for IFx-2.0, designed to be used in conjunction with Keytruda® for advanced or metastatic Merkel Cell Carcinoma, and if successful, it will significantly enhance the company's competitiveness in the cancer treatment market.
- Technological Innovation: The company is advancing TBS-2025, an antibody drug targeting mutNPM1 relapsed/refractory acute myeloid leukemia, into Phase 2 development, which, if successful, will further enrich TuHURA's product pipeline and strengthen its market position.
- Strategic Acquisition: TuHURA's merger with Kineta Inc. has brought TBS-2025 into its portfolio, demonstrating its expansion strategy in cancer immunotherapy aimed at addressing primary and acquired resistance issues in cancer treatments.
See More
TuHURA Files IND for TBS-2025 in AML Treatment
- New Drug Application: TuHURA Biosciences has filed an Investigational New Drug (IND) application with the FDA for TBS-2025, aimed at treating mutNPM1 relapsed/refractory Acute Myeloid Leukemia (AML) in combination with a menin inhibitor, potentially improving patient response rates.
- Clinical Trial Design: The company plans to initiate a Phase 2 clinical trial in menin inhibitor-naïve patients in early Q2 2026, utilizing a Simon 2 stage design, with preliminary results expected in Q3 2026, demonstrating ongoing commitment to this therapeutic area.
- Scientific Rationale: Research indicates that mutations like mutNPM1 may drive VISTA expression on leukemic cells, leading to poor treatment responses; TuHURA believes that adding TBS-2025 could significantly enhance both the CR/CRh rates and their duration, addressing unmet medical needs.
- Safety Assessment: TBS-2025 has shown a favorable safety profile in early trials at a maximum dose of 1,000mg every two weeks, with the optimal Phase 2 dose projected at 750mg every three weeks, laying a solid foundation for further clinical development.
See More
