Global Blood Therapeutics, Inc. (NASDAQ:GBT) Files An 8-K Other Events

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Global Blood Therapeutics, Inc. (NASDAQ:GBT) Files An 8-K Other Events

Item 8.01. Other Events.

On June 28, 2017, Global Blood Therapeutics, Inc. issued a press
release announcing that its GBT440 therapy for the treatment of
sickle cell disease (SCD) has been granted access by the European
Medicines Agency (EMA) to the EMAs Priority Medicines (PRIME)
program (the Press Release). A copy of the Press Release is filed
herewith as Exhibit 99.1 and is incorporated herein by reference.

Item 9.01. Financial Statements and Exhibits.

(d) Exhibits


Exhibit No.


Description


99.1


Press Release, dated June 28, 2017



Global Blood Therapeutics, Inc. Exhibit
EX-99.1 2 exh_991.htm PRESS RELEASE EdgarFilingEXHIBIT 99.1Global Blood Therapeutics Receives EMA PRIME Designation for GBT440 for the Treatment of Sickle Cell Disease (SCD) – GBT440 is First Potential Treatment for SCD To Be Accepted for PRIME – – PRIME Designation Allows for Frequent and Early Interactions with the Agency Aimed at Assisting Accelerated Evaluation and Approval – SOUTH SAN FRANCISCO,…
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About Global Blood Therapeutics, Inc. (NASDAQ:GBT)

Global Blood Therapeutics, Inc. is a clinical-stage biopharmaceutical company. The Company is engaged in discovering, developing and commercializing therapeutics to treat blood-based disorders. The Company’s segment is engaged in discovering, developing and commercializing therapeutics to treat blood-based disorders. It is developing its initial product candidate, GBT440, as an oral, once-daily therapy for sickle cell disease (SCD) and is evaluating GBT440 in SCD subjects in an ongoing Phase I/II clinical trial. SCD is a genetic disease marked by red blood cell (RBC) destruction and occluded blood flow and hypoxia, leading to anemia, stroke, multi-organ failure, severe pain crises, and shortened patient life span. GBT440 inhibits abnormal hemoglobin polymerization, the underlying mechanism of RBC sickling. It is also engaged in other research and development activities targeted towards hereditary angioedema (HAE).