$LABT

Lakewood-Amedex Biotherapeutics Inc.

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Lakewood-Amedex Biotherapeutics Inc. (LABT): Submission of Matters to a Vote of Security Holders

Lakewood-Amedex Biotherapeutics Inc. (LABT) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. Item 5.07. Submission of Matters to a Vote of Security Holders. On September 22, 2026, Lakewood-Amedex Biotherapeutics Inc. (the “Company”) held its 2026 Annual Meeting of Stockholders (the “Annual Meeting”). As of the record date of July 30, 2026, there were 2,369,688 shares of

Lakewood-Amedex doses first patient in Phase 2a trial for Diabetic foot infections

Lakewood-Amedex Biotherapeutics dosed the first patient in a Phase 2a trial for Nu-3, a gel treating mildly infected diabetic foot ulcers. The trial will assess safety, efficacy, and optimal dosage. Results are expected in Q1 2027, with potential Phase 2b advancement if successful. According to the company, Nu-3 aims to reduce antimicrobial resistance by targeting infections locally.

Lakewood-Amedex Biotherapeutics Announces First Patient Dosed in Phase 2a Clinical Trial of Nu-3 for Infected Diabetic Foot Ulcers

Lakewood-Amedex Biotherapeutics Inc. (NASDAQ: LABT) has dosed the first patient in its Phase 2a clinical trial for Nu-3, a topical antimicrobial gel for infected diabetic foot ulcers. The trial aims to evaluate safety and efficacy of three gel concentrations, with topline data expected in Q1 2027. Nu-3 is part of the company's Bisphosphocin® antimicrobial platform.

LABT sentiment & insider activity

Over the past 7 days, AlphAI's AI scored 2 news stories mentioning LABT (Lakewood-Amedex Biotherapeutics Inc.). Coverage has skewed bullish: 1 bullish, 1 neutral, and 0 bearish.

Recent LABT coverage spans technology, corporate actions and market movers.

What's driving LABT

AlphAI scores every news story that mentions LABT with an AI model for sentiment and relevance, and aggregates insider trades from Lakewood-Amedex Biotherapeutics Inc.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $LABT

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$LABTLow

Lakewood-Amedex Biotherapeutics Inc. (LABT): Submission of Matters to a Vote of Security Holders

Lakewood-Amedex Biotherapeutics Inc. (LABT) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. Item 5.07. Submission of Matters to a Vote of Security Holders. On September 22, 2026, Lakewood-Amedex Biotherapeutics Inc. (the “Company”) held its 2026 Annual Meeting of Stockholders (the “Annual Meeting”). As of the record date of July 30, 2026, there were 2,369,688 shares of

$LABTMedAI 8/10

Lakewood-Amedex doses first patient in Phase 2a trial for Diabetic foot infections

Lakewood-Amedex Biotherapeutics dosed the first patient in a Phase 2a trial for Nu-3, a gel treating mildly infected diabetic foot ulcers. The trial will assess safety, efficacy, and optimal dosage. Results are expected in Q1 2027, with potential Phase 2b advancement if successful. According to the company, Nu-3 aims to reduce antimicrobial resistance by targeting infections locally.

Lakewood-Amedex Biotherapeutics Announces First Patient Dosed in Phase 2a Clinical Trial of Nu-3 for Infected Diabetic Foot Ulcers

Lakewood-Amedex Biotherapeutics Inc. (NASDAQ: LABT) has dosed the first patient in its Phase 2a clinical trial for Nu-3, a topical antimicrobial gel for infected diabetic foot ulcers. The trial aims to evaluate safety and efficacy of three gel concentrations, with topline data expected in Q1 2027. Nu-3 is part of the company's Bisphosphocin® antimicrobial platform.

Lakewood-Amedex Biotherapeutics CEO Issues Letter to Shareholders Highlighting Transformational Progress and Outlook for Nu-3

Lakewood-Amedex Biotherapeutics (LABT) reported Q2 2026 progress, including Nasdaq listing, $7.5M private placement, and Nu-3 Gel Phase 2a trial prep. The company expanded its IP portfolio and appointed David G. Armstrong as Study Chair. LABT aims to advance Nu-3 for infected diabetic foot ulcers, with clinical trial initiation expected soon.

$LABTMedAI 8/10

Lakewood-Amedex Biotherapeutics Announces IRB Approval and Clinical Site Readiness to Initiate Phase 2a Clinical Trial of Nu-3 for the Treatment of Infected Diabetic Foot Ulcers

Lakewood-Amedex Biotherapeutics (NASDAQ: LABT) received IRB approvals and clinical site readiness to start a Phase 2a trial for its lead product, Nu-3, treating infected diabetic foot ulcers. The trial aims to evaluate Nu-3's safety and efficacy, building on positive preclinical data. The company aims to address antibiotic-resistant bacterial strains with its Bisphosphocin® class of antimicrobials.

$LABTMedAI 8/10

Lakewood-Amedex Biotherapeutics Announces IRB Approval and Clinical Site Readiness to Initiate Phase 2a Clinical Trial of Nu-3 for the Treatment of Infected Diabetic Foot Ulcers

Lakewood-Amedex Biotherapeutics (NASDAQ: LABT) received IRB approvals and confirmed clinical site readiness to start a Phase 2a trial for Nu-3, a treatment for infected diabetic foot ulcers. The trial aims to evaluate safety and efficacy, building on positive preclinical data. The company focuses on addressing antibiotic-resistant bacterial infections with its Bisphosphocin® class of antimicrobials.

$LABTLow

Lakewood-Amedex Highlights Nu-3 Resistance Data In Support Of National Action Plan; Stock Up

Lakewood-Amedex Biotherapeutics (LABT) said it presented new data on its antimicrobial candidate Nu-3 for infected diabetic foot ulcers. The company reported a high barrier to resistance in serial passage tests and broad in vitro activity against multiple resistant bacteria mechanisms. LABT linked the findings to the National Action Plan discussed at a June 2026 PACCARB meeting. LABT closed at $1.86.

Lakewood-Amedex Biotherapeutics Announces Preclinical Safety Data Supporting Clinical Dose Selection for Upcoming Phase 2a Trial of Nu-3 Gel

Lakewood-Amedex Biotherapeutics (NASDAQ: LABT) said preclinical safety data for its Nu-3 topical gel supported dose selection for an upcoming Phase 2a trial in infected diabetic foot ulcers. The company reported Nu-3 was well tolerated in an FDA-required safety study at higher doses, with low systemic exposure and no wound-healing inhibition. Planned gel concentrations are 2%, 5%, and 10%.

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