Skip to main content
LABTNasdaq

Lakewood-Amedex Biotherapeutics Inc.

Pharmaceutical preparations·University Park, FL, United States·CEO: Dr. Kelvin Cooper Ph.D.

LABT 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 LABT—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · LABT

Lakewood-Amedex Biotherapeutics Inc. (LABT) is a clinical-stage biopharmaceutical company focused on developing its lead antimicrobial candidate Nu-3, having recently strengthened its balance sheet through a Series C financing and Nasdaq listing, though it remains pre-revenue and requires additional capital to complete development.

Key risk: Going concern uncertainty

5.8/10

BioSniper Score

Based on 2 of 6 signals

Limited data coverage

Market Cap

$5.5M

Cash Runway

6.5 mo

Lead Asset

Next Catalyst

Financial data as of Jun 30, 2026.

AI OverviewAI overview is shown in English only.

Lakewood-Amedex Biotherapeutics Inc. (LABT) is a clinical-stage biopharmaceutical company focused on developing its lead antimicrobial candidate Nu-3, having recently strengthened its balance sheet through a Series C financing and Nasdaq listing, though it remains pre-revenue and requires additional capital to complete development.

  • Lead product candidate Nu-3 is being advanced toward a Phase 2a dose-comparison clinical study [sec_mda · as of 2026-08-14].
  • Completed a Series C Convertible Preferred Stock financing in Q2 2026, generating approximately $7.5 million in gross proceeds [sec_mda · as of 2026-08-14].
  • Listed its common stock on the Nasdaq Capital Market during the quarter ended June 30, 2026 [sec_mda · as of 2026-08-14].
  • As of June 30, 2026, the company held cash, cash equivalents, and certificates of deposit sufficient to support near-term operating objectives of less than 12 months [sec_mda · as of 2026-08-14].
  • The company has incurred recurring operating losses since inception and expects to continue incurring losses as it advances clinical development [sec_mda · as of 2026-08-14].

What works

  • The company substantially improved its liquidity and working capital position during the six months ended June 30, 2026, primarily through the Series C financing and conversion of preferred stock and convertible debt into common stock [sec_mda · as of 2026-08-14].
  • The Nasdaq listing and simplified capital structure position the company to advance its clinical development plans [sec_mda · as of 2026-08-14].
  • The company employs an outsourced model for manufacturing and clinical activities, which management believes enables capital efficiency and focus on pipeline advancement [sec · filed 2026-05-01].

What to weigh

  • The company has no approved products and has not generated any revenue from product sales [sec · filed 2026-05-01].
  • As of June 30, 2026, the company had cash and equivalents of $2.6 million and a net loss of $3.8 million for the period, with shareholders' equity of only $0.4 million [latest reported financials].
  • Management expects that additional capital will be required to complete clinical development, pursue regulatory approvals, and support commercialization activities [sec_mda · as of 2026-08-14].
  • The company's independent registered public accounting firm has expressed substantial doubt about its ability to continue as a going concern [sec · filed 2026-05-01].

From the filings

Quoted directly from source documents.

  • The company completed a Series C financing and Nasdaq listing in Q2 2026, strengthening its balance sheet.

    During the quarter, the Company completed a private placement of its Series C Convertible Preferred Stock, generating approximately $7.5 million in gross proceeds, completed the listing of its common stock on the Nasdaq Capital Market, and substantially simplified its capital structure through the conversion of its outstanding preferred stock and convertible debt into common stock.

    SEC MD&A · August 14, 2026

  • The company has incurred recurring operating losses since inception.

    The Company has incurred recurring operating losses since inception and expects to continue incurring losses as it advances the clinical development of Nu-3 and its other product candidates.

    SEC MD&A · August 14, 2026

  • The company's auditors have raised substantial doubt about its ability to continue as a going concern.

    ited financial statements for the years ended December 31, 2025 and 2024 include an explanatory paragraph from our independent registered public accounting firm stating that our recurring losses from operations raise substantial doubt about our ability to continue as a going concern.

    SEC filings · May 1, 2026

Risks & what to watch (4)

Key risks

  • Going concern uncertaintyAuditors have expressed substantial doubt about the company's ability to continue as a going concern due to recurring losses [sec · filed 2026-05-01].
  • Need for additional capitalManagement expects additional capital will be required to complete clinical development and pursue regulatory approvals [sec_mda · as of 2026-08-14].
  • No revenue or approved productsThe company has no products approved for commercial sale and has not generated any revenue from product sales [sec · filed 2026-05-01].
  • Clinical development risksNu-3 is still in early clinical stages; Phase 2a study has not yet commenced and outcomes are uncertain [sec_mda · as of 2026-08-14].

What to watch

  • Initiation and results of the Phase 2a dose-comparison clinical study for Nu-3 [sec_mda · as of 2026-08-14].
  • Ability to secure additional financing to extend cash runway beyond the current 12-month estimate [sec_mda · as of 2026-08-14].
  • Progress in preclinical development of additional pipeline candidates and any IND filings [sec · filed 2026-05-01].
  • Any updates on the company's ability to generate revenue or enter into collaborations [sec · filed 2026-05-01].

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

Run Lakewood-Amedex Biotherapeutics Inc. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available Lakewood-Amedex Biotherapeutics Inc. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 2 of 6 signals · derived from public data

No clinical pipeline tracked — this score reflects financial & catalyst signals only.

Cash Runway1.8

6.5 months

Financial Health9.8

D/E 0.15 · 0% dilution

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Financials

Governance

Frequently asked questions

What is the AI investment thesis for Lakewood-Amedex Biotherapeutics Inc.?

Lakewood-Amedex Biotherapeutics Inc. (LABT) is a clinical-stage biopharmaceutical company focused on developing its lead antimicrobial candidate Nu-3, having recently strengthened its balance sheet through a Series C financing and Nasdaq listing, though it remains pre-revenue and requires additional capital to complete development.

Who is the CEO of Lakewood-Amedex Biotherapeutics Inc.?

Dr. Kelvin Cooper Ph.D. is the chief executive officer of Lakewood-Amedex Biotherapeutics Inc. (LABT).

Where is Lakewood-Amedex Biotherapeutics Inc. headquartered?

Lakewood-Amedex Biotherapeutics Inc. (LABT) is headquartered in University Park, FL, United States.

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.