TuHURA Biosciences to Present at the H.C. Wainwright 28th Annual Global Investment Conference
TuHURA Biosciences will outline its late-stage immuno-oncology pipeline in a fireside chat at the H.C. Wainwright Global Investment Conference.
Rhea-AI Summary
TuHURA Biosciences (HURA) will present at the H.C. Wainwright 28th Annual Global Investment Conference in New York on Monday, September 14 at 4:00 p.m. ET.
The presentation will be a fireside chat with associated 1x1 meetings. The company provides online registration for live viewing, and an archived webcast of the fireside chat will be made available on the Events page in the investor section of TuHURA’s website.
TuHURA is a Phase 3 immuno-oncology company focused on overcoming primary and acquired resistance to cancer immunotherapy. Its lead candidate, IFx-2.0, is in a randomized, placebo-controlled Phase 3 registration trial as an adjunct to Keytruda in first-line advanced or metastatic Merkel Cell Carcinoma, and it is also advancing TBS-2025 and Delta Opioid Receptor-based ADC programs.
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Key Terms
immuno-oncology medical
placebo-controlled medical
mAb medical
ADCs medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
H.C. Wainwright 28th Annual Global Investment Conference | |
Date: | Monday, September 14th |
Time: | 4:00pm ET |
Format: | Fireside Chat & 1x1 Meetings |
To register and view the presentation, please CLICK HERE.
An archived webcast of the Fireside Chat will be available on the Events Page in the investor section of TuHURA's website.
About TuHURA Biosciences, Inc.
TuHURA Biosciences, Inc. (NASDAQ: HURA) is a Phase 3 immuno-oncology company developing novel technologies to overcome primary and acquired resistance to cancer immunotherapy, two of the most common reasons cancer immunotherapies fail to work or stop working in the majority of patients with cancer.
TuHURA's lead innate immune agonist, IFx-2.0, is designed to overcome primary resistance to checkpoint inhibitors. TuHURA is enrolling patients in its randomized placebo-controlled Phase 3 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.
In addition to its innate immune agonist product candidates, TuHURA is developing TBS-2025, a VISTA inhibiting mAb moving into dose escalation/optimization Phase 1b trial in mutNPM1 r/r AML, a molecularly defined subgroup representing approximately
For more information, please visit www.tuhurabio.com and connect with TuHURA on Facebook, X, and LinkedIn.
Investor Contact:
Monique Kosse
Gilmartin Group
Monique@GilmartinIR.com

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SOURCE TuHURA Biosciences, Inc.
FAQ
When and in what format will TuHURA Biosciences present at the H.C. Wainwright conference?
The TuHURA Biosciences presentation is scheduled for Monday, September 14 at 4:00 p.m. ET. It will be held as a fireside chat, with additional 1x1 meetings during the H.C. Wainwright 28th Annual Global Investment Conference in New York, NY.
How can investors access TuHURA Biosciences’ conference presentation and replay?
Investors can register and view the presentation through an online registration link provided by TuHURA. An archived webcast of the fireside chat will be available after the event on the Events Page in the investor section of TuHURA’s website.
What is TuHURA Biosciences’ lead clinical program IFx-2.0?
IFx-2.0 is TuHURA’s lead innate immune agonist designed to overcome primary resistance to checkpoint inhibitors. The company is enrolling patients in a randomized, placebo-controlled Phase 3 registration trial of IFx-2.0 given as an adjunctive therapy to Keytruda (pembrolizumab) compared with Keytruda plus placebo in first-line treatment of advanced or metastatic Merkel Cell Carcinoma.
What other pipeline programs is TuHURA Biosciences advancing?
TuHURA is developing TBS-2025, a VISTA-inhibiting monoclonal antibody moving into dose escalation/optimization Phase 1b in mutNPM1 relapsed/refractory AML, a molecularly defined subgroup that represents approximately 35% of AML patients. The company is also leveraging its Delta Opioid Receptor technology to create first-in-class, bi-specific, bi-functional antibody drug conjugates targeting myeloid-derived suppressor cells (MDSCs) to reduce immune suppression in the tumor microenvironment and address acquired resistance to checkpoint inhibitors and cellular therapies.