ADMA Biologics to Virtually Participate in the Cantor Healthcare Conference

Rhea-AI Summary

ADMA Biologics (Nasdaq: ADMA) will participate in a virtual fireside chat at the Cantor Healthcare Conference on September 30, 2021, at 9:20 a.m. ET. Adam Grossman, President and CEO, will lead the discussion. A webcast of the event will be available on the company’s website and archived for 90 days. ADMA specializes in the manufacturing and marketing of plasma-derived biologics, currently offering three FDA-approved products for immunodeficient patients and those at risk of infectious diseases. The company operates an FDA-licensed facility in Boca Raton, Florida.

Positive

• Participation in the Cantor Healthcare Conference enhances visibility and investor engagement.
• ADMA has three FDA-approved plasma-derived biologics, indicating a solid product portfolio.

Negative

• None.

RAMSEY, N.J. and BOCA RATON, Fla., Sept. 23, 2021 (GLOBE NEWSWIRE) -- ADMA Biologics, Inc. (Nasdaq: ADMA) (the “Company”), an end-to-end commercial biopharmaceutical company dedicated to manufacturing, marketing and developing specialty plasma-derived biologics, today announced that Adam Grossman, President and Chief Executive Officer, will participate in a virtual fireside chat at the Cantor Healthcare Conference on September 30, 2021, at 9:20 a.m. ET.

A webcast of the event will be available on the Company’s website at https://ir.admabiologics.com/events-webcasts and will be archived for 90 days following the event.

About ADMA Biologics, Inc. (ADMA)

ADMA Biologics is an end-to-end American commercial biopharmaceutical company dedicated to manufacturing, marketing and developing specialty plasma-derived 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 U.S., which provides a portion of its blood plasma for the manufacture of its products. 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 management of immune compromised patient populations who suffer from an underlying immune deficiency, or who may be immune compromised for other medical reasons. ADMA has received U.S. Patents: 9,107,906, 9,714,283, 9,815,886, 9,969,793 and 10,259,865 related to certain aspects of its products and product candidates. For more information, please visit www.admabiologics.com.

COMPANY CONTACT:
Skyler Bloom
Director, Investor Relations and Corporate Strategy | 201-478-5552 | sbloom@admabio.com

INVESTOR RELATIONS CONTACT:
Michelle Pappanastos
Senior Managing Director, Argot Partners | 212-600-1902 | michelle@argotpartners.com

FAQ

When will ADMA Biologics participate in the Cantor Healthcare Conference?

ADMA Biologics will participate in the Cantor Healthcare Conference on September 30, 2021, at 9:20 a.m. ET.

Who will represent ADMA Biologics at the conference?

Adam Grossman, President and CEO of ADMA Biologics, will represent the company at the conference.

Where can I watch the ADMA Biologics conference webcast?

The webcast of the ADMA Biologics conference will be available on the company's website.

What products does ADMA Biologics offer?

ADMA Biologics offers three FDA-approved plasma-derived biologics for immunodeficient patients.