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CRISPR Therapeutics AG. (5/15/18). "Press Release: CRISPR Therapeutics Announces Presentations at the ASGCT 21st Annual Meeting". Zug & Cambridge, MA.

Region Region Chicago, IL
  Country United States (USA)
Organisations Organisation CRISPR Therapeutics AG (Nasdaq: CRSP)
  Group CRISPR Therapeutics (Group)
  Organisation 2 American Society of Gene and Cell Therapy (ASGCT)
Products Product CRISPR gene editing technology
  Product 2 ASGCT 2018 Chicago
Persons Person Ho, Tony (CRISPR Therapeutics 201708– EVP + Head RnD)
  Person 2 Paganelli, Jennifer (W2O Group 201703)

CRISPR Therapeutics (NASDAQ:CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious diseases, today announced that members of the CRISPR team will make a series of presentations at the American Society of Gene & Cell Therapy (ASGCT) Annual Meeting being held May 16-19, 2018 at the Hilton Chicago.

Title: Gene Editing Workshop
Presenter: Tirtha Chakraborty, Ph.D., Head of Hematology, CRISPR Therapeutics
Time and Date: Tuesday, May 15, 4:00 PM CT
Location: Hilton Chicago, Continental C

Title: Induction of HbF to Treat ß-hemoglobinopathies – Bringing CRISPR to the Clinic
Presenter: Tony Ho, M.D., Head of Research and Development, CRISPR Therapeutics
Time and Date: Friday, May 18, 8:00 AM CT
Location: Hilton Chicago, International Ballroom North

Title: Allogeneic CAR T Cells with Multiple Therapeutically Favorable Edits Can Be Created Efficiently Using CRISPR/Cas9
Presenter: Melanie Allen, Scientist, CRISPR Therapeutics
Time and Date: Friday, May 18, 2018: 5:45 PM CT
Location: Hilton Chicago, P792, Stevens Salon C, D

Title: Efficient Clinical Scale CRISPR/Cas9-Mediated Editing of Plerixafor-Mobilized Hematopoietic Stem and Progenitor CD34+ Cells for Treatment of Sickle Cell Disease
Presenter: Hui Yu, Ph.D., Scientist, CRISPR Therapeutics
Time and Date: Saturday, May 19, 11:30 AM
Location: Hilton Chicago, Salon A-3,4

About CRISPR Therapeutics

CRISPR Therapeutics is a leading gene editing company focused on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. CRISPR/Cas9 is a revolutionary gene editing technology that allows for precise, directed changes to genomic DNA. The Company has established a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology and rare diseases. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic collaborations with leading companies including Bayer AG and Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Cambridge, Massachusetts, and business offices in London, United Kingdom. For more information, please visit


CRISPR Therapeutics

Jennifer Paganelli
WCG on behalf of CRISPR
+1 347-658-8290

Chris Erdman
+1 617-307-7227

Chris Brinzey
Westwicke Partners for CRISPR
+1 339-970-2843

Record changed: 2018-06-01


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