ADMA Biologics to Participate in the Jefferies Virtual Plasma Summit

Rhea-AI Summary

ADMA Biologics, Inc. (Nasdaq: ADMA) announced that CEO Adam Grossman will participate in a fireside chat at the Jefferies Virtual Plasma Summit on March 11, 2021, at 11:20 a.m. ET. Interested parties can view the event via a webcast on the company’s website, which will be archived for 90 days post-event. The company specializes in manufacturing and marketing FDA-approved plasma-derived biologics aimed at treating immunodeficient patients and preventing infectious diseases. ADMA's key products include BIVIGAM®, ASCENIV™, and NABI-HB®.

RAMSEY, N.J. and BOCA RATON, Fla., March 04, 2021 (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 plasma-derived biologics, today announced that Adam Grossman, President and Chief Executive Officer, will participate in a fireside chat at the upcoming Jefferies Virtual Plasma Summit being held on Thursday, March 11, 2021, at 11:20 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:
Sam Martin
Managing Director, Argot Partners | 212-600-1902 | sam@argotpartners.com

FAQ

When will ADMA participate in the Jefferies Virtual Plasma Summit?

ADMA will participate in the Jefferies Virtual Plasma Summit on March 11, 2021, at 11:20 a.m. ET.

How can I watch the ADMA presentation at the Plasma Summit?

You can watch ADMA's presentation via a webcast available on the company's website, which will be archived for 90 days afterwards.

What are the main products of ADMA Biologics?

ADMA Biologics' main products include BIVIGAM®, ASCENIV™, and NABI-HB®, all of which are FDA-approved plasma-derived biologics.

What is the focus of ADMA Biologics as a company?

ADMA Biologics focuses on manufacturing and developing specialty plasma-derived biologics for immunodeficient patients and the management of infectious diseases.