3 Growth Stocks for In-the-Know Investors

07:35am, Wednesday, 16'th Dec 2020
They aren't household names, but they're experiencing significant catalysts for growth.
One aspect of the ANEW ETF is focused on the bleeding edge of medical advances. Here's what you need to know if you're considering investing.
The biotech just filed to advance its second pipeline candidate into clinical testing.
EDIT-301 is in development as a best-in-class, durable medicine for people living with sickle cell disease
Momentum continues from the biotech's weekend presentation of promising data for its experimental sickle cell disease therapy.

Why Editas Medicine Stock Jumped Again Today

03:41pm, Tuesday, 08'th Dec 2020
Momentum continued from the biotech's positive update announced over the weekend.
One metric shows that decades of dominance treating diabetes has created unrivaled profitability.

Why Editas Medicine Stock Is Soaring Today

11:41am, Monday, 07'th Dec 2020
Investors liked the biotech's update about experimental gene-editing therapy EDIT-301.
Data support novel approach to develop and manufacture a best-in-class, durable medicine for people living with hemoglobinopathies
Editas has foundational expertise in CRISPR technology. It has recently entered clinical trials using its platform in a rare eye disease.
CAMBRIDGE, Mass., Nov. 10, 2020 (GLOBE NEWSWIRE) -- Editas Medicine, Inc. (Nasdaq: EDIT), a leading genome editing company, today announced the grant of inducement awards to the Company's newly appoin
CAMBRIDGE, Mass., Nov. 09, 2020 (GLOBE NEWSWIRE) -- Editas Medicine, Inc. (Nasdaq: EDIT), a leading genome editing company, today announced that it named Lisa A. Michaels, M.D., as the Company's Execu
Editas Medicine, Inc. (EDIT) CEO Cindy Collins on Q3 2020 Results - Earnings Call Transcript
CAMBRIDGE, Mass., Oct. 29, 2020 (GLOBE NEWSWIRE) -- Editas Medicine, Inc. (Nasdaq: EDIT), a leading genome editing company, today announced that it will host a conference call and webcast on Thursda
Using a gene-editing technique that won a recent Nobel Prize, Crispr Therapeutics cleared blood cancers in patients with off-the-shelf immune cells. Previously, a patient’s own cells were required.
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