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INTI

Inhibitor Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Pre-clinical·Tampa, FL, United States·CEO: Dr. Francis E. O'Donnell Jr., M.D.
OncologyDermatology

INTI evidence brief

What we can confirm

BioSniper Score:
2.4 / 10
Market Cap:
$17.5M
Lead Asset:
suba-itraconazole (Preclinical)

What it means

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

What to watch

Market Cap: $17.5M · Lead Asset: suba-itraconazole (Preclinical)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · INTI

Inhibitor Therapeutics, Inc. (INTI) is a pharmaceutical development company focused on developing and commercializing innovative therapeutics, currently advancing an itraconazole program for Basal Cell Carcinoma Nevus Syndrome (Gorlin Syndrome) with a revised regulatory strategy and a novel formulation under development.

Key risk: Low cash runway

2.4/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$17.5M

Cash Runway

—

Lead Asset

suba-itraconazole (Preclinical)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 1 clinical trial for Inhibitor Therapeutics, Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Inhibitor Therapeutics, Inc. (INTI) is a pharmaceutical development company focused on developing and commercializing innovative therapeutics, currently advancing an itraconazole program for Basal Cell Carcinoma Nevus Syndrome (Gorlin Syndrome) with a revised regulatory strategy and a novel formulation under development.

  • Cash & equivalents of $0.5M as of 2026-06-30 [sec]
  • Net income of -$0.6M as of 2026-06-30 [sec]
  • Shareholders' equity of -$2.6M as of 2026-06-30 [sec]
  • Revised regulatory strategy for itraconazole in Basal Cell Carcinoma Nevus Syndrome (BCCNS) [news · 2026-09-08]
  • Engaged Avior Bio, Inc. to develop a novel formulation of itraconazole; PK crossover study expected to take approximately six weeks [sec_mda · as of 2026-03-26]

What works

  • The company has a revised regulatory strategy for itraconazole in BCCNS, indicating active progress in its lead program [news · 2026-09-08]
  • Avior Bio has completed formulation development for a novel itraconazole formulation, and a PK crossover study is underway to support a new pre-IND and NDA [sec_mda · as of 2026-03-26]

What to weigh

  • Cash & equivalents are very low at $0.5M as of 2026-06-30, which may constrain operations and development [sec]
  • Shareholders' equity is negative at -$2.6M as of 2026-06-30, indicating accumulated losses exceed equity [sec]
  • The company's net income was -$0.6M as of 2026-06-30, reflecting ongoing operating losses [sec]

From the filings

Quoted directly from source documents.

  • Revised regulatory strategy for itraconazole in BCCNS

    “Recent progress includes a revised regulatory strategy for itraconazole in Basal Cell Carcinoma Nevus Syndrome”

    News · September 8, 2026

  • PK crossover study expected to take approximately six weeks

    “The PK crossover study is expected to take approximately six weeks to comple”

    SEC MD&A · March 26, 2026

Risks & what to watch (3)›

Key risks

  • Low cash runway — Cash & equivalents of only $0.5M as of 2026-06-30 may limit ability to fund operations and development [sec]
  • Negative shareholders' equity — Shareholders' equity of -$2.6M as of 2026-06-30 indicates accumulated losses exceed equity [sec]
  • Ongoing net losses — Net income of -$0.6M as of 2026-06-30 reflects continued operating losses [sec]

What to watch

  • Completion of the PK crossover study for the novel itraconazole formulation, expected to take approximately six weeks from March 2026 [sec_mda · as of 2026-03-26]
  • Outcome of the revised regulatory strategy for itraconazole in BCCNS [news · 2026-09-08]
  • Annual stockholder meeting on September 15, 2026, where key developments may be discussed [news · 2026-09-08]

Sources: News · SEC MD&A · Generated October 8, 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 Health2.0

Net income -$614K

Pipeline Maturity2.0

Lead: Preclinical

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Regulatory

Financials

Short Interest

as of Apr 30, 2026
% of float
0.4%
Days to cover
0.1
Shares short
19,880
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 →

INTI short interest

Frequently asked questions

What is the AI investment thesis for Inhibitor Therapeutics, Inc.?

Inhibitor Therapeutics, Inc. (INTI) is a pharmaceutical development company focused on developing and commercializing innovative therapeutics, currently advancing an itraconazole program for Basal Cell Carcinoma Nevus Syndrome (Gorlin Syndrome) with a revised regulatory strategy and a novel formulation under development.

What is Inhibitor Therapeutics, Inc.'s lead drug candidate?

Inhibitor Therapeutics, Inc.'s most advanced tracked candidate is suba-itraconazole (Preclinical) for Lung cancer.

Who is the CEO of Inhibitor Therapeutics, Inc.?

Dr. Francis E. O'Donnell Jr., M.D. is the chief executive officer of Inhibitor Therapeutics, Inc. (INTI).

Where is Inhibitor Therapeutics, Inc. headquartered?

Inhibitor Therapeutics, Inc. (INTI) is headquartered in Tampa, FL, United States.

What therapeutic areas does Inhibitor Therapeutics, Inc. focus on?

Inhibitor Therapeutics, Inc. develops therapies across Oncology, Dermatology.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)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.