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Telomir Pharmaceuticals raises US$5.6M in PIPE for breast cancer trial

The Oct. 5 placement issued 4.84 million shares at US$1.16 each and gave the placement agent warrants for another 387,464 shares.

Adrian Kessler·
An oversized sealed petri dish stands on the wet paving of an anonymous biomedical research courtyard at blue hour.
An oversized sealed petri dish in a research courtyard. Illustration: Mugglehead, generated with AI.

A US$5.6 million private share sale closed on Oct. 5 as Telomir Pharmaceuticals, Inc. NASDAQTELO prepares its first human study of Telomir-Zn in advanced breast cancer, its SEC filing shows. The 4,843,300 shares issued at US$1.16 each provide funding for a Phase 1/2 trial and working capital.

The fixed share price was five per cent below the stock's applicable 10-day volume-weighted average price, measured two days before closing. Investors received no warrants or convertible securities, although Telomir issued separate warrants to its placement agent.

Telomir is a Miami-based clinical-stage biotechnology company developing small-molecule therapeutics, led by its oral breast cancer candidate Telomir-Zn.

Telomir shares closed at US$1.20 on Nasdaq on Oct. 6, down 0.8 per cent as of 4 p.m. EDT NASDAQTELO. The Oct. 6 filing requires a resale registration statement for the placement shares within 30 days of the Oct. 5 closing.

Agent Warrants Add Potential Shares

Telomir agreed to pay Alexander Capital a placement-agent cash fee, according to its Oct. 6 filing. The company also agreed to reimburse documented expenses of up to US$40,000.

The agent or its designees received warrants to buy 387,464 additional shares at US$1.16 each. Those warrants can be exercised for cash and expire five years after issuance, while the placement shares were sold without investor warrants or price-reset provisions.

The newly issued stock equals roughly seven per cent of the 68.78 million shares Google Finance listed as outstanding at 4 p.m. EDT on Oct. 6 NASDAQTELO. That comparison uses total shares outstanding because the transaction filing does not state the freely tradable share count; exercising the agent warrants would add more shares.

Existing shareholder John Paul DeJoria invested an additional US$1 million, Telomir said in its Oct. 6 announcement. Other existing shareholders and new investors participated, but the release did not identify their individual subscriptions or give a revised cash-runway estimate.

"As Telomir enters clinical development, our focus is on execution: deploying this capital efficiently to advance Telomir-Zn through its Phase 1/2 clinical program, generate meaningful human data and position the Company strongly for the milestones ahead."

Telomir chief executive Erez Aminov said this in the company's Oct. 6 release.

Telomir's Release Gives No First Dose Date

The company said the U.S. Food and Drug Administration had cleared its investigational new drug application for a multicentre, open-label Phase 1/2 trial in advanced or metastatic triple-negative breast cancer. The first stage will assess safety, tolerability and dose selection, with a later expansion focused more closely on efficacy.

Telomir describes Telomir-Zn as an oral drug candidate intended to alter intracellular metal balance and gene regulation. The Oct. 6 release cites preclinical work, while giving no date for the first patient dose, trial readout or submission of human efficacy data.

A dated financing comparison comes from Sernova Biotherapeutics Inc. TSESVA OTCMKTSSEOVF. Its Oct. 5 release said Seraxis Holdings, Inc. closed a US$11.2 million financing in convertible notes and warrants tied to their planned merger. Seraxis expects first patient dosing in its diabetes cell-therapy trial in the first quarter of 2027, giving that raise a dated clinical target.

Read more: Sernova and Seraxis close US$11.2M financing for diabetes trial

Read more: Orexo AB (publ) proposes SEK250M rights issue ahead of drug milestones

By Nov. 4, Telomir is due to file a resale registration statement with the SEC for the new shares. Filing by then would meet that 30-day requirement; the Oct. 6 release does not give a date for the first trial dose.

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