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SEC Filing · ARS

ADMA Biologics Inc

ADMANASDAQEQUITYCurrent

SEC Filing

Filed Apr 15, 2026Accepted Apr 15, 2026, 4:40 PM EDTCIK 1368514Accession 0001140361-26-014803
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Company context

ADMA Biologics is a U.S.-based, 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: ASCENIV™ (immune globulin intravenous, human - slra 10% liquid) for the treatment of primary humoral immunodeficiency (PI); BIVIGAM® (immune globulin intravenous, human) for the treatment of PI; and NABI-HB® (hepatitis B immune globulin, human) to provide enhanced immunity against the hepatitis B virus. Additionally, ADMA is developing SG-001, a pre-clinical, investigative hyperimmune globulin targeting S. pneumonia. ADMA manufactures its immune globulin products and product candidates 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 U.S., which provides its blood plasma for the manufacture of its products and product candidates. ADMA’s mission is to manufacture, market and develop specialty plasma-derived, human immune globulins targeted to niche patient populations for the treatment and prevention of certain infectious diseases and m

Current securities

Recent company filings

  1. 10-Q filingAug 5, 2026
  2. Results of Operations and Financial ConditionAug 5, 2026
  3. Submission of Matters to a Vote of Security HoldersJun 2, 2026
  4. 10-Q filingMay 6, 2026
  5. Results of Operations and Financial ConditionMay 6, 2026

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