Welcome to our dedicated page for Revium Recovery SEC filings (Ticker: RVRC), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Revium Recovery Inc’s biotechnology disclosures are packed with nanoparticle pharmacokinetics, clinical trial protocols, and licensing clauses—details crucial to gauging future breakthroughs yet buried in hundreds of pages. Finding when executives purchase shares before a trial read-out or pinpointing dilution risk from a new financing round shouldn’t require a PhD.
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Revium Rx is registering up to 1,562,500 Units in a self-underwritten primary offering and up to 37,625,790 shares of common stock for resale by existing stockholders. Each Unit consists of two common shares and one warrant, offered at a fixed price of $3.20 per Unit, with expected net proceeds to the company of about $4.4 million if all Units are sold. Common shares outstanding would rise from 60,729,100 to 63,854,100, excluding shares issuable on new IPO warrants.
The company is a preclinical biotechnology business developing lipid-based drug delivery platforms for antimicrobial resistance, oncology and immunology, built around liposomal and nano-medicine technologies licensed from Hebrew University’s Yissum and acquired via its LipoVation transaction. Revium Rx has a history of losses, expects continued negative cash flow, and will need substantial additional funding beyond this offering.
Key risks include early-stage product candidates with no regulatory approvals, complex and uncertain clinical and regulatory paths, heavy reliance on licensed intellectual property, potential dilution from warrants and resales, penny-stock trading on the OTC market, and operational and geopolitical risks tied to significant R&D activities in Israel and multi-front regional conflict.
Revium Rx (RVRC) filed an amended S-1 registering a self-underwritten primary offering of 1,562,500 Units at a fixed public offering price of $3.20 per Unit (each Unit = two shares + one warrant) and a resale registration for up to 37,625,790 shares by selling stockholders. The Company expects $4,400,000 in net proceeds if all Units sell and no IPO warrants are exercised, and proposes to allocate approximately 55% (~$2.42M) to advance Nano-Mupirocin, 25% (~$1.1M) to Nano-ARB work, and 20% (~$880k) to G&A.
The filing discloses material risks including a history of losses, substantial future funding needs, potential dilution from existing warrants and resale shares, penny-stock trading restrictions, dependence on key officers, IP and regulatory risks for its nanoformulations, and operational exposure from Israeli geopolitical instability. The document also states an existing Non-Clinical Evaluation Agreement with NIAID and exclusive license rights for LPLT vaccine technology, with a SARS-CoV-2 challenge study expected to resume in Q4 2025 and conclude in Q1 2026.
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