Intelligent Bio Solutions Inc

Noticias y eventos de Intelligent Bio Solutions Inc (INBS)

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Noticias de INBS

Eventos de INBS

9/1 09:00

Intelligent Bio Solutions Enters Agreement to Issue 2,036,659 Shares

Intelligent Bio Solutions announced that it has entered into a securities purchase agreement with a single existing institutional investor to issue, in a private placement priced at-the-market under Nasdaq rules, 2,036,659 shares of common stock (or Series M pre-funded warrants in lieu thereof), Series N-1 warrants to purchase up to an aggregate of 2,036,659 shares of common stock, and Series N-2 warrants to purchase up to an aggregate of 2,036,659 shares of common stock, at a combined purchase price of $2.455 per share of common stock (or Series M pre-funded warrant) and associated Series N-1 warrants and Series N-2 warrants, for expected gross proceeds to INBS of approximately $5.0 million, before deducting placement agent fees and other offering expenses payable by the Company. Ladenburg Thalmann & Co. Inc. is acting as the exclusive placement agent for the private placement.

8/11 09:30

Intelligent Bio Solutions Completes Drug Screening Study

Intelligent Bio Solutions announced the completion of its multi-site Method Comparison Study for the Intelligent Fingerprinting Drug Screening System, one of several studies underpinning the company's FDA 510(k) submission for U.S. market clearance for detection of the opiate codeine. All clinical data collection across the company's FDA 510(k) clinical study program is now complete. The study was conducted across three independent U.S. clinical sites over three weeks in partnership with CenExel Clinical Research. A total of 135 participants were enrolled. The company now moves into analysis, compilation, and finalization of its 510(k) submission package, targeting submission in the second half of 2026, ahead of planned entry into the multi-billion-dollar U.S. market.

7/21 09:00

Intelligent Bio Solutions Completes Precision Testing

Intelligent Bio Solutions announced the completion of precision testing, a key component of the company's FDA 510 submission for U.S. market clearance of its Intelligent Fingerprinting Drug Screening System for detection of the opiate codeine. The precision testing, conducted following the Company's clinical cut-off adjustment, confirmed that the Intelligent Fingerprinting Drug Screening System produced consistent, reliable results across varied manufacturing conditions and operating environments. The precision testing included more than 1,600 tests across three production runs and three independent sites. The results showed repeatable, reproducible performance across all runs and sites, confirming the system's suitability for workplace and other drug screening environments.

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