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INTIOTC

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

No verified snapshot fields are available yet.

What it means

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

What to watch

Watch the next source-backed data update.
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 based on already approved active pharmaceuticals with patent-protected methods of use or delivery, currently advancing a new formulation of itraconazole toward an NDA submission.

Key risk: Cash runway uncertainty

1.6/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$15.6M

Cash Runway

2.1 mo

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 based on already approved active pharmaceuticals with patent-protected methods of use or delivery, currently advancing a new formulation of itraconazole toward an NDA submission.

  • Pharmaceutical development company focused on already approved active pharmaceuticals with patent-protected methods of use or delivery [sec_mda · as of 2026-08-14].
  • Cash and equivalents of $0.5M as of 2026-06-30 [sec].
  • Net income of -$0.6M for the period ended 2026-06-30 [sec].
  • Shareholders' equity of -$1.3M as of 2026-06-30 [sec].
  • Zero total debt as of 2026-06-30 [sec].

What works

  • The company is developing a new formulation of itraconazole, an already approved active pharmaceutical, which may allow for a streamlined NDA submission without additional clinical trials if the FDA agrees [sec_mda · as of 2025-11-13].
  • The company has no debt, reducing financial leverage risk [sec].
  • The company has a clear regulatory pathway strategy: using a crossover PK study to demonstrate comparable levels of itraconazole to a prior FDA-approved formulation [sec_mda · as of 2025-11-13].

What to weigh

  • Cash and equivalents have declined significantly from $7.7M (March 2024) to $0.5M (June 2026), indicating a rapid cash burn rate [sec_mda · as of 2024-05-13] [sec].
  • Shareholders' equity is negative (-$1.3M as of 2026-06-30), suggesting accumulated losses exceed assets [sec].
  • The company's ability to continue operations is uncertain given the low cash balance and ongoing net losses [sec].
  • The FDA has not yet concluded whether additional clinical trials are required before NDA submission, creating regulatory uncertainty [sec_mda · as of 2025-05-14].

From the filings

Quoted directly from source documents.

  • The company's strategy involves using a new formulation of itraconazole and a crossover PK study to justify NDA submission without additional clinical trials.

    Utilizing the new formulation of itraconazole as the API (Active Pharmaceutical Ingredient) which has been developed with Avior, coupled with a crossover PK study to demonstrate that our formulation of itraconazole delivers comparable levels of itraconazole as the itraconazole formulation used in prior clinical trials, and approved by the FDA, we intend to obtain justification for the submission of an NDA without requiring additional clinical trials.

    SEC MD&A · November 13, 2025

  • Cash on hand was approximately $4.3 million as of March 31, 2025.

    Our current cash on hand, approximately $4.3 million as of March 31, 2025, is sufficient to continue to execute our busines

    SEC MD&A · May 14, 2025

  • The company expects to progress with the FDA to determine if additional clinical trials are needed before NDA submission.

    We expect to progress with the FDA to reach a conclusion on whether any additional clinical trials are required before submitting our New Drug Application (NDA).

    SEC MD&A · May 14, 2025

Risks & what to watch (4)

Key risks

  • Cash runway uncertaintyCash of only $0.5M as of 2026-06-30 may be insufficient to fund operations without additional financing [sec].
  • Negative shareholders' equityShareholders' equity of -$1.3M as of 2026-06-30 indicates accumulated losses exceed assets [sec].
  • FDA regulatory uncertaintyFDA has not yet decided if additional clinical trials are needed before NDA submission, which could delay or increase costs [sec_mda · as of 2025-05-14].
  • Dependence on single productThe company's pipeline is focused on a single itraconazole formulation, with no diversified product portfolio [sec_mda · as of 2025-11-13].

What to watch

  • FDA decision on whether additional clinical trials are required before NDA submission [sec_mda · as of 2025-05-14].
  • Company's ability to secure additional financing given low cash balance [sec].
  • Progress of the crossover PK study for the new itraconazole formulation [sec_mda · as of 2025-11-13].
  • Any updates on cash runway or operational plans in future SEC filings [sec_mda · as of 2026-08-14].

Sources: SEC MD&A · Generated August 28, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash Runway0.6

2.1 months

Financial Health0.5

OCF -$775K · 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

Runway

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 based on already approved active pharmaceuticals with patent-protected methods of use or delivery, currently advancing a new formulation of itraconazole toward an NDA submission.

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.

925 companies232,681 SEC filings21,419 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.