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    ADMA Biologics to Report Third Quarter 2024 Financial Results on November 7, 2024

    10/29/24 4:10:00 PM ET
    $ADMA
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care
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    RAMSEY, N.J. and BOCA RATON, Fla., Oct. 29, 2024 (GLOBE NEWSWIRE) -- ADMA Biologics, Inc. (NASDAQ:ADMA) ("ADMA" or the "Company"), an end-to-end commercial biopharmaceutical company dedicated to manufacturing, marketing, and developing specialty biologics, today announced that it will report third quarter 2024 financial results on November 7, 2024, after the U.S. financial markets close. ADMA's management team will host a live conference call and audio webcast on that date at 4:30 p.m. ET to discuss its financial results and other Company updates.

    To access the conference call, please dial (888) 596-4144 and refer to conference ID 2959956. It is recommended that you join approximately 10 minutes prior to the event start (although you may dial in at any time during the call). Attendees who will not be asking a question during the call are encouraged to listen in to the live webcast here. An archived replay of the event will be available located under "Events & Webcasts" in the investor section of the Company's website at https://ir.admabiologics.com/events-webcasts.

    About ADMA Biologics, Inc. (ADMA)

    ADMA Biologics is an end-to-end commercial biopharmaceutical company dedicated to manufacturing, marketing and developing specialty biologics for the treatment of immunodeficient patients at risk for infection and others at risk for certain infectious diseases. ADMA currently manufactures and markets three United States Food and Drug Administration (FDA)-approved plasma-derived biologics for the treatment of immune deficiencies and the prevention of certain infectious diseases: BIVIGAM® (immune globulin intravenous, human) for the treatment of primary humoral immunodeficiency (PI); ASCENIV™ (immune globulin intravenous, human – slra 10% liquid) for the treatment of PI; and NABI-HB® (hepatitis B immune globulin, human) to provide enhanced immunity against the hepatitis B virus. ADMA manufactures its immune globulin products at its FDA-licensed plasma fractionation and purification facility located in Boca Raton, Florida. Through its ADMA BioCenters subsidiary, ADMA also operates as an FDA-approved source plasma collector in the United States, which provides its blood plasma for the manufacture of its products. ADMA's mission is to manufacture, market and develop specialty biologics and human immune globulins targeted to niche patient populations for the treatment and prevention of certain infectious diseases and management of immune compromised patient populations who suffer from an underlying immune deficiency, or who may be immune compromised for other medical reasons. ADMA holds numerous U.S. and foreign patents related to and encompassing various aspects of its products and product candidates. For more information, please visit www.admabiologics.com.

    INVESTOR RELATIONS CONTACT:

    Michelle Pappanastos

    Senior Managing Director, Argot Partners | 212-600-1902 | [email protected]



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    Q&A

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    • When will ADMA Biologics report its third quarter 2024 financial results?

      ADMA Biologics will report its third quarter 2024 financial results on November 7, 2024.

    • What time will the conference call to discuss ADMA's financial results take place?

      ADMA's management team will host a conference call and audio webcast at 4:30 p.m. ET on the same day that the financial results are announced.

    • How can one join the conference call for ADMA Biologics' financial results?

      To access the conference call, dial (888) 596-4144 and use conference ID 2959956.

    • What are the main products offered by ADMA Biologics?

      ADMA Biologics manufactures and markets three FDA-approved plasma-derived biologics for treating immune deficiencies and preventing infectious diseases.

    • Where does ADMA Biologics manufacture its products and how do they source their plasma?

      ADMA Biologics operates an FDA-licensed facility in Boca Raton, Florida, and collects source plasma through its subsidiary, ADMA BioCenters.

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