ADMA Biologics to Participate in the Jefferies Virtual Healthcare Conference

Rhea-AI Summary

ADMA Biologics, Inc. (Nasdaq: ADMA) announced that CEO Adam Grossman will participate in a fireside chat at the Jefferies Virtual Healthcare Conference on June 2, 2021, at 4:00 p.m. ET. The event will be accessible via a webcast on ADMA's website and will be archived for 90 days. ADMA is committed to developing specialty plasma-derived biologics for immunodeficient patients and currently offers three FDA-approved products: BIVIGAM®, ASCENIV™, and NABI-HB®. The company operates an FDA-licensed facility in Boca Raton, Florida, focusing on plasma fractionation and purification.

RAMSEY, N.J. and BOCA RATON, Fla., May 26, 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 fireside chat at the Jefferies Virtual Healthcare Conference on June 2, 2021 at 4:00 p.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

What is the date and time of ADMA's fireside chat at the Jefferies Virtual Healthcare Conference?

The fireside chat will take place on June 2, 2021, at 4:00 p.m. ET.

Where can I watch the ADMA Biologics fireside chat?

The event will be available via a webcast on ADMA's website, with an archive for 90 days.

What are the FDA-approved products offered by ADMA Biologics?

ADMA offers BIVIGAM®, ASCENIV™, and NABI-HB® as its FDA-approved products.

What is the focus of ADMA Biologics?

ADMA Biologics focuses on developing and manufacturing plasma-derived biologics for immunodeficient patients.

Where is ADMA Biologics located?

ADMA operates its FDA-licensed facility in Boca Raton, Florida.