Rocket Pharmaceuticals Announces Participation at Upcoming October 2018 Conferences

Sept. 25, 2018 11:00 UTC

- Gaurav Shah, M.D., Chief Executive Officer, Invited as Panel Member at The Galien Forum USA 2018 -

NEW YORK--(BUSINESS WIRE)-- Rocket Pharmaceuticals, Inc. (NASDAQ: RCKT) (“Rocket”), a leading U.S.-based multi-platform gene therapy company, today announced that members of Rocket’s executive team will participate in the following upcoming conferences:

  • Cantor Fitzgerald Global Healthcare Conference on October 1, 2018, at 9:30 a.m. Eastern Time in New York, NY
  • Ladenburg Thalmann 2018 Healthcare Conference on October 2, 2018, at 11:30 a.m. Eastern Time in New York, NY
  • Leerink Partners Roundtable Series: Rare Disease & Oncology on October 2, 2018, at 1:30 p.m. Eastern Time in New York, NY
  • Chardan Genetic Medicines Conference on October 9, 2018, at 2:00 p.m. Eastern Time in New York, NY
  • Gene Therapy Panel during The Galien Forum USA 2018 on October 25, 2018, at 2:40 p.m. Eastern Time in New York, NY

A live audio webcast of the Ladenburg presentation will be available on the Investors section of the company’s website, www.rocketpharma.com. A replay of the presentation will be archived on the Rocket website following the conference.

About Rocket Pharmaceuticals, Inc.

Rocket Pharmaceuticals, Inc. (NASDAQ: RCKT) (“Rocket”) is an emerging, clinical-stage biotechnology company focused on developing first-in-class gene therapy treatment options for rare, devastating diseases. Rocket’s multi-platform development approach applies the well-established lentiviral vector (LVV) and adeno-associated viral vector (AAV) gene therapy platforms. Rocket's lead clinical program is a LVV-based gene therapy for the treatment of Fanconi Anemia (FA), a difficult to treat genetic disease that leads to bone marrow failure and potentially cancer. Preclinical studies of additional bone marrow-derived disorders are ongoing and target Pyruvate Kinase Deficiency (PKD), Leukocyte Adhesion Deficiency-I (LAD-I) and Infantile Malignant Osteopetrosis (IMO). Rocket is also developing an AAV-based gene therapy program for an undisclosed rare pediatric disease. For more information about Rocket, please visit www.rocketpharma.com.

 

Contacts

Claudine Prowse, Ph.D.
SVP, Corporate Strategy and IRO
Rocket Pharma, Inc.
The Empire State Building, Suite 7530
New York, NY 10118
cp@rocketpharma.com
www.rocketpharma.com
investors@rocketpharma.com

 
 

Source: Rocket Pharmaceuticals, Inc.

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