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NRXP

NRX Pharmaceuticals Inc.

Biopharma developer (SEC filing verified)·Commercial·Wilmington, DE, United States·CEO: Dr. Jonathan C. Javitt M.D., M.P.H.
NeurologyInfectious Disease

NRXP evidence brief

What we can confirm

BioSniper Score:
6.2 / 10
Market Cap:
$124.3M
Lead Asset:
htx-100 (Preclinical)

What it means

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

What to watch

Market Cap: $124.3M · Lead Asset: htx-100 (Preclinical)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · NRXP

NRX Pharmaceuticals Inc. (NRXP) is a clinical-stage biopharmaceutical company developing ketamine-based therapies for central nervous system disorders, with a preservative-free ketamine ANDA under FDA review and a subsidiary focused on robotic TMS systems.

Key risk: Pending ANDA vial attestation

6.2/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$124.3M

Cash Runway

—

Lead Asset

htx-100 (Preclinical)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates for NRX Pharmaceuticals Inc..

AI OverviewAI overview is shown in English only.

NRX Pharmaceuticals Inc. (NRXP) is a clinical-stage biopharmaceutical company developing ketamine-based therapies for central nervous system disorders, with a preservative-free ketamine ANDA under FDA review and a subsidiary focused on robotic TMS systems.

  • Cash & equivalents of $26.7M as of 2026-06-30 [sec].
  • Total revenue of $1.1M and net income of -$16.5M as of 2026-06-30 [sec].
  • Completed first-cycle FDA review of ANDA for preservative-free ketamine with no drug-related major deficiencies; sole remaining item is a manufacturer's attestation on the vial [news · 2026-08-17].
  • FDA reclassified the ANDA amendment from Major to Minor and set a GDUFA goal date of November 10, 2026 [news · 2026-09-15].
  • Subsidiary HOPE Therapeutics began training to deploy Zeta Surgical's FDA-cleared robotic TMS system in Florida clinics [news · 2026-09-11].

What works

  • Strong cash position of $26.7M as of 2026-06-30 provides runway for operations and commercialization [sec].
  • First-cycle FDA review of preservative-free ketamine ANDA found no drug-related major deficiencies, indicating a clear regulatory path [news · 2026-08-17].
  • FDA reclassification of the ANDA amendment from Major to Minor suggests a lower regulatory burden and faster path to approval [news · 2026-09-15].
  • Subsidiary HOPE Therapeutics is deploying an FDA-cleared robotic TMS system, potentially expanding the company's pipeline into neuroplastic treatments [news · 2026-09-11].

What to weigh

  • Net loss of -$16.5M as of 2026-06-30 indicates ongoing operational losses [sec].
  • Shareholders' equity is negative (-$0.2M as of 2026-06-30), suggesting liabilities exceed assets [sec].
  • The ANDA for preservative-free ketamine still has a pending manufacturer's attestation on the vial, which could delay approval [news · 2026-08-17].
  • The company's pipeline includes preclinical-stage candidates (e.g., htx-100) with no near-term revenue prospects [pipeline].

From the filings

Quoted directly from source documents.

  • FDA reclassification of ANDA amendment

    “Abbreviated New Drug Application (ANDA) Amendment related to the drug vial for preservative-free ketamine has been reclassified from a Major Amendment to a Minor Amendment.”

    News · September 15, 2026

  • First-cycle FDA review with no drug-related major deficiencies

    “Completed first-cycle FDA review of the Company’s ANDA for preservative-free ketamine with no drug-related major deficiencies.”

    News · August 17, 2026

  • Deployment of robotic TMS system

    “HOPE is the first Interventional Psychiatry network to deploy Zeta Surgical's newly FDA-cleared TMS Robotic System”

    News · September 11, 2026

Risks & what to watch (4)›

Key risks

  • Pending ANDA vial attestation — FDA approval of preservative-free ketamine hinges on a manufacturer's attestation on the vial, which has been submitted but not yet accepted [news · 2026-08-17].
  • Negative shareholders' equity — Shareholders' equity of -$0.2M as of 2026-06-30 indicates liabilities exceed assets, raising solvency concerns [sec].
  • Preclinical pipeline uncertainty — Key pipeline candidate htx-100 is preclinical, with no near-term revenue and competitive landscape of 12 competitors [pipeline].
  • Operational net loss — Net loss of -$16.5M as of 2026-06-30 reflects ongoing operational losses with limited revenue of $1.1M [sec].

What to watch

  • FDA decision on preservative-free ketamine ANDA by GDUFA goal date of November 10, 2026 [news · 2026-09-15].
  • Commercial launch of preservative-free ketamine with 5 million doses planned for 2026 [news · 2026-08-17].
  • Deployment and clinical results of Zeta Surgical's robotic TMS system in HOPE Therapeutics' Florida clinics [news · 2026-09-11].
  • Progress of NRx Defense Systems subsidiary in developing neuroplastic treatments with D-cycloserine and TMS [sec · filed 2026-07-22].

Sources: News · Pipeline · SEC filings · Generated October 4, 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 -$17M

Pipeline Maturity9.5

Lead: BLA Filed

Pipeline Breadth7.2

4 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Financials

Short Interest

as of Apr 30, 2026
% of float
10.4%
Days to cover
3.6
Shares short
3,248,961
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 →

NRXP short interest

Governance

Frequently asked questions

What is the AI investment thesis for NRX Pharmaceuticals Inc.?

NRX Pharmaceuticals Inc. (NRXP) is a clinical-stage biopharmaceutical company developing ketamine-based therapies for central nervous system disorders, with a preservative-free ketamine ANDA under FDA review and a subsidiary focused on robotic TMS systems.

What is NRX Pharmaceuticals Inc.'s lead drug candidate?

NRX Pharmaceuticals Inc.'s most advanced tracked candidate is htx-100 (Preclinical) for Suicidal depression, PTSD, and other serious Central Nervous System (CNS) disorders.

Who is the CEO of NRX Pharmaceuticals Inc.?

Dr. Jonathan C. Javitt M.D., M.P.H. is the chief executive officer of NRX Pharmaceuticals Inc. (NRXP).

Where is NRX Pharmaceuticals Inc. headquartered?

NRX Pharmaceuticals Inc. (NRXP) is headquartered in Wilmington, DE, United States.

What therapeutic areas does NRX Pharmaceuticals Inc. focus on?

NRX Pharmaceuticals Inc. develops therapies across Neurology, Infectious Disease.

923 companies304,840 SEC filings22,636 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.