Mesabi Trust Announces News Release
Distribution Announcement: Mesabi Trust declared a distribution of $0.34 per Unit of Beneficial Interest, payable on November 20, 2025, which is a decrease from the $0.39 distribution from the previous year.
Factors Influencing Distribution: The Trustees' decision reflects total royalty payments received from Cleveland-Cliffs Inc. and considerations for maintaining reserves to cover current and future expenses amid uncertainties in the iron ore and steel industries.
Royalty Payments Timeline: Quarterly royalty payments from Cliffs and Northshore for the third calendar quarter are due on October 30, 2025, and a summary report will be filed with the SEC following receipt.
Forward-Looking Statements: The announcement includes forward-looking statements regarding Northshore operations and potential risks that could affect actual production and royalty payments, emphasizing the inherent uncertainties in the industry.
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Mesabi Trust (MSB) Declares $0.26 Quarterly Dividend Payable February 20
- Quarterly Dividend Announcement: Mesabi Trust declares a $0.26 per share dividend, reflecting the company's ongoing cash flow and profitability, which is likely to attract more investor interest.
- Record Date for Shareholders: The record date for this dividend is set for January 30, meaning investors holding shares before this date will qualify for the dividend, enhancing short-term shareholder confidence.
- Ex-Dividend Date Arrangement: The ex-dividend date is also set for January 30, requiring investors to purchase shares before this date to receive the dividend, which may lead to increased trading activity leading up to this date.
- Payment Date Confirmation: The dividend will be paid on February 20, ensuring shareholders receive their returns promptly, further solidifying the company's reputation in the capital markets.

Mesoblast Receives FDA Feedback for BLA Filing of rexlemestrocel-L
- FDA Feedback: Mesoblast has received feedback from the FDA regarding its allogeneic cell therapy product, rexlemestrocel-L, indicating plans to file a Biologics License Application (BLA), marking a significant advancement in chronic discogenic low back pain treatment.
- Clinical Trial Results: In the MSB-DR003 randomized controlled Phase 3 trial, the FDA acknowledged the efficacy of rexlemestrocel-L in reducing chronic low back pain, with significant pain intensity reduction observed at 12 months, potentially supporting product efficacy.
- Labeling Update: The FDA noted that robust results on opioid use reduction from at least one adequate and well-controlled trial could be included in the Clinical Studies section of the product labeling, enhancing market competitiveness.
- RMAT Designation: rexlemestrocel-L has been designated as a Regenerative Medicine Advanced Therapy (RMAT) by the FDA, providing all the benefits of Breakthrough and Fast Track programs, including rolling review and priority review eligibility, further accelerating the path to market.






