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CRISPR THERAPEUTICS AG (NASDAQ:CRSP) Files An 8-K Results of Operations and Financial Condition

CRISPR THERAPEUTICS AG (NASDAQ:CRSP) Files An 8-K Results of Operations and Financial ConditionItem 2.02.

Results of Operations and Financial Condition.

On August10, 2017, CRISPR Therapeutics AG announced its financial results for the second quarter ended June30, 2017.The full text of the press release issued in connection with the announcement is furnished as Exhibit 99.1 to this Current Report on Form8-K.

The information in this Form 8-K (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such a filing.

Item 2.02. Financial Statements and Exhibits.

(d)Exhibits:

The following exhibits shall be deemed to be furnished, and not filed:

Exhibit No.

Description

99.1 Press Release by CRISPR Therapeutics AG, dated August 10, 2017

CRISPR Therapeutics AG ExhibitEX-99.1 2 d441068dex991.htm EX-99.1 EX-99.1 Exhibit 99.1   CRISPR Therapeutics Announces Second Quarter 2017 Financial Results and Provides Business Update On track to file for clinical trial application (CTA) for lead program in beta-thalassemia in 2017 Rapid progress in immuno-oncology including a lead program in allogeneic CAR-T cell therapy Expanded foundational and therapeutic intellectual property position Strong financial position to support development of pipeline and fund operations ZUG,…To view the full exhibit click here
About CRISPR THERAPEUTICS AG (NASDAQ:CRSP)
Crispr Therapeutics AG is a Switzerland-based gene-editing company. The Company focuses on the development of transformative gene-based medicines for serious diseases using its Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 gene-editing platform. CRISPR/Cas9 can be programmed to cut, edit and correct disease-associated deoxyribonucleic acid (DNA) in a patient’s cell. The location at which the Cas9 molecular scissors cut the DNA to be edited is specified by guide ribonucleic acid (RNA), which is comprised of a crRNA component and a tracrRNA component, either individually or combined together as a single guide RNA. The Company has business operations in London, the United Kingdom, as well as research and development operations in Cambridge, the United States.

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