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GTBPGT Biopharma, Inc.
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$5.51▲ 1.85%vs prev close
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  • 4d agoPre-market26.10.21 13:15filed
    EFFECTOther#●●●#●●●

    GT Biopharma, Inc.

    GT Biopharma's registration statement was declared effective by the SEC on October 20, 2026. This effectiveness allows the company to proceed with the issuance or sale of the registered securities.…more

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  • 4d agoAfter-hours26.10.21 06:20
    424B3Offering

    GT Biopharma, Inc.

    GT Biopharma has filed a registration statement for the resale of up to 13,502,835 shares of common stock, which may be issued upon the conversion of Series M and Series L preferred stock and the exercise of associated warrants. This prospectus facilitates potential sales by selling stockholders, and the company will not receive any proceeds from these transactions.…more

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  • 10.13After-hours26.10.14 06:00
    DEF 14AOther

    GT Biopharma, Inc.

    GT Biopharma will hold a Special Meeting of Stockholders on November 11, 2026, to vote on increasing authorized common shares from 25 million to 250 million. The meeting will also seek approval for the issuance of 19.99% or more of outstanding common stock related to the September 14, 2026, Securities Purchase Agreement, including shares issuable upon conversion of Series M Preferred Stock and exercise of warrants. These measures are intended to support corporate purposes and facilitate the conversion and exercise of existing securities.…more

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  • 10.9After-hours26.10.10 06:32
    Bullish#●●●

    GT Biopharma Files Prospectus for Offering of Up to 13.5M Shares

    GT Biopharma has filed a prospectus with the SEC regarding the potential sale of up to 13,502,835 shares by selling stockholders. This filing indicates a potential increase in the number of shares available for trading, which may lead to share dilution.…more

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  • 9.15Pre-market26.09.15 22:16

    ●●●●●●●● ●●●●● ●●●●●●

    GT Biopharma has received FDA clearance for its IND application for GTB-5550 to treat multiple myeloma. The initiation of the Phase 1 trial remains contingent upon the receipt of non-dilutive grant funding.…more

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  • 9.15Pre-market26.09.15 21:45

    ●●●●●●●● ●●●●● ●●●●●●

    GT Biopharma has secured FDA clearance to initiate human clinical trials for its multiple myeloma treatment candidate, GTB-5550. The start of the trial remains contingent upon the receipt of non-dilutive grant funding.…more

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