Inventera Wins FDA Approval for Phase 1 Trial of INV-003 Contrast Agent

Bitget2026/10/19 01:42

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Inventera received FDA clearance on Oct. 16, 2026, for a Phase 1 trial of INV-003, its oral MRCP contrast agent.
The US trial will enroll up to 30 adults to assess safety, tolerability and imaging efficacy.
Completion is expected by Oct. 17, 2027, with results intended to establish the recommended Phase 2 dose.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Inventera Inc. published the original content used to generate this news brief via DART, the regulatory disclosure system operated by the South Korea Financial Supervisory Service (FSS) (Ref. ID: 20261019900151), on October 19, 2026, and is solely responsible for the information contained therein.

Disclaimer: The content of this article solely reflects the author's opinion and does not represent the platform in any capacity. This article is not intended to serve as a reference for making investment decisions.

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Inventera Wins FDA Approval for Phase 1 Trial of INV-003 Contrast Agent

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