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HURA

TuHURA Biosciences, Inc./NV

Biopharma developer (SEC filing verified)·Phase 3·Tampa, FL, United States·CEO: Dr. James A. Bianco M.D.
Oncology

HURA evidence brief

What we can confirm

BioSniper Score:
7.3 / 10
Market Cap:
$130.6M
Lead Asset:
ifx2.0 (Phase 3)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $130.6M · Lead Asset: ifx2.0 (Phase 3)
BioSniper AIPage context preserved

Prepared research question

What matters most for HURA—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · HURA

TuHURA Biosciences, Inc. (HURA) is a Phase 3 immuno-oncology company developing novel therapeutics to overcome resistance to cancer immunotherapy, with a lead Phase III program in Merkel cell carcinoma and a recently cleared IND for a VISTA-inhibiting antibody in AML.

Key risk: Low cash runway

7.3/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$130.6M

Cash Runway

—

Lead Asset

ifx2.0 (Phase 3)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates for TuHURA Biosciences, Inc./NV.

Similar companies

AI OverviewAI overview is shown in English only.

TuHURA Biosciences, Inc. (HURA) is a Phase 3 immuno-oncology company developing novel therapeutics to overcome resistance to cancer immunotherapy, with a lead Phase III program in Merkel cell carcinoma and a recently cleared IND for a VISTA-inhibiting antibody in AML.

  • Cash & equivalents of $1.0M as of 2026-06-30 [sec].
  • Net income of -$9.2M for the quarter ended 2026-06-30 [sec].
  • Shareholders' equity of $18.5M as of 2026-06-30 [sec].
  • Phase III trial of IFx-Hu2.0 in first-line advanced Merkel cell carcinoma is ongoing [news · published 2026-08-14].
  • FDA cleared IND for TBS-2025 VISTA-inhibiting antibody for molecularly defined subsets of AML and other blood-related cancers on 2026-09-14 [news · published 2026-09-14].

What works

  • Lead program IFx-Hu2.0 has advanced to a Phase III randomized, double-blind, placebo-controlled trial in Merkel cell carcinoma, a late-stage milestone [catalyst].
  • The company secured a $50 million loan facility, which management believes is sufficient to provide a cash runway [news · published 2026-05-26].
  • FDA clearance of the IND for TBS-2025 opens a new clinical pathway in AML and blood-related cancers, expanding the pipeline beyond solid tumors [news · published 2026-09-14].

What to weigh

  • Cash position is very low at $1.0M as of 2026-06-30, indicating a need for near-term financing or revenue [sec].
  • Net loss of $9.2M in the most recent quarter (ended 2026-06-30) reflects ongoing operating deficits [sec].
  • The VISTA-inhibitor space is crowded, with at least 363 competitors including Merck and other large pharma players [pipeline].
  • Phase III readout for IFx-Hu2.0 is not expected until early 2026, leaving a period of binary event risk [news · published 2025-11-18].

From the filings

Quoted directly from source documents.

  • FDA clearance of IND for TBS-2025 in AML and blood-related cancers

    “the U.S. Food and Drug Administration (FDA) has given clearance to TuHURA's Investigational New Drug (IND) application for its TBS-2025 VISTA-inhibiting antibody for molecularly defined subsets of Acute Myeloid Leukemia (AML) and other blood-related cancers.”

    News · September 14, 2026

  • Phase III trial of IFx-Hu2.0 in Merkel cell carcinoma is ongoing

    “A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of IFx-Hu2.0 as an Adjunctive Therapy to Pembrolizumab in Checkpoint-Inhibitor Naïve Participants With Advanced or Metastatic Merkel Cell Carcinoma”

    Catalysts

Catalyst timeline

  • 2025-10-01 · Phase1_Start: IFx-Hu2.0 As An Adjunctive Therapy To Pembrolizumab In Checkpoint Inhibitor Naïve Subjects With Advanced Or Metastatic Merkel Cell Carcinoma — Initiation of a Phase 1 study for IFx-Hu2.0 in Merkel cell carcinoma.
  • 2025-12-11 · Phase3_Start: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of IFx-Hu2.0 as an Adjunctive Therapy to Pembrolizumab in Checkpoint-Inhibitor Naïve Participants With Advanced or Metastatic Merkel Cell Carcinoma — Start of the pivotal Phase 3 trial for IFx-Hu2.0 in Merkel cell carcinoma.
Risks & what to watch (4)›

Key risks

  • Low cash runway — Cash & equivalents of only $1.0M as of 2026-06-30 may require near-term financing [sec].
  • Ongoing net losses — Net loss of $9.2M in the most recent quarter (ended 2026-06-30) indicates continued cash burn [sec].
  • Competitive VISTA landscape — 363 competitors in the VISTA-inhibitor space, including Merck and other large pharma [pipeline].
  • Binary Phase III outcome — Phase III readout for IFx-Hu2.0 expected in early 2026, creating a binary event risk [news · published 2025-11-18].

What to watch

  • Phase III readout for IFx-Hu2.0 in Merkel cell carcinoma, expected early 2026 [news · published 2025-11-18].
  • Initiation of Phase Ib/II trial for TBS-2025 in AML following IND clearance [news · published 2026-09-14].
  • Company's ability to secure additional financing given low cash position [sec].
  • Presentation at H.C. Wainwright conference on 2026-09-08 may provide pipeline updates [news · published 2026-09-08].

Sources: Catalysts · News · Pipeline · Generated October 13, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health8.9

D/E 0.72 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth4.6

2 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

88

Total value held

$16.8M

Showing top 10 of 88 institutional holders of TuHURA Biosciences, Inc./NV. Open the full 13F history after sign-in.

Short Interest

as of May 21, 2026
% of float
16.8%
Days to cover
6.3
Shares short
8,260,038
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

HURA short interest

Governance

Frequently asked questions

What is the AI investment thesis for TuHURA Biosciences, Inc./NV?

TuHURA Biosciences, Inc. (HURA) is a Phase 3 immuno-oncology company developing novel therapeutics to overcome resistance to cancer immunotherapy, with a lead Phase III program in Merkel cell carcinoma and a recently cleared IND for a VISTA-inhibiting antibody in AML.

What is TuHURA Biosciences, Inc./NV's lead drug candidate?

TuHURA Biosciences, Inc./NV's most advanced tracked candidate is ifx2.0 (Phase 3).

Who is the CEO of TuHURA Biosciences, Inc./NV?

Dr. James A. Bianco M.D. is the chief executive officer of TuHURA Biosciences, Inc./NV (HURA).

Where is TuHURA Biosciences, Inc./NV headquartered?

TuHURA Biosciences, Inc./NV (HURA) is headquartered in Tampa, FL, United States.

What therapeutic areas does TuHURA Biosciences, Inc./NV focus on?

TuHURA Biosciences, Inc./NV develops therapies across Oncology.

923 active companies304,861 SEC filings22,725 clinical trials
Citation log window (7 days): 13,363 recorded LLM calls; 0 block events, 0 warning events. These counts do not measure factual accuracy or research quality.Computed at
How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.