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NASDAQ:CRSP

CRISPR Therapeutics Q2 2026 Earnings Report

CRISPR Therapeutics logo
$51.72 -0.54 (-1.03%)
Closing price 09/11/2026 04:00 PM Eastern
Extended Trading
$51.76 +0.05 (+0.09%)
As of 09/11/2026 07:47 PM Eastern
Extended trading is trading that happens on electronic markets outside of regular trading hours. This is a fair market value extended hours price provided by Massive. Learn more.

CRISPR Therapeutics EPS Results

Actual EPS
-$0.94
Consensus EPS
-$1.19
Beat/Miss
Beat by +$0.25
One Year Ago EPS
-$2.40

CRISPR Therapeutics Revenue Results

Actual Revenue
$10.18 million
Expected Revenue
$7.45 million
Beat/Miss
Beat by +$2.73 million
YoY Revenue Growth
+1,033.30%

CRISPR Therapeutics Announcement Details

Quarter
Q2 2026
Time
After Market Closes
Conference Call Date
Monday, August 3, 2026
Conference Call Time
4:00PM ET

Upcoming Earnings

CRISPR Therapeutics' Q3 2026 earnings is estimated for Monday, November 9, 2026, based on past reporting schedules, with a conference call scheduled on Tuesday, November 3, 2026 at 4:00 PM ET. Check back for transcripts, audio, and key financial metrics as they become available.

CRISPR Therapeutics Earnings Headlines

Trump's New Dollar
Porter Stansberry says President Trump has signed an executive order initiating what he calls a full U.S. dollar reset - and most Americans don't know it's happening. The last time America underwent a monetary shift like this, under Nixon in the 1970s, it minted an average of 1,300 new millionaires a day for over half a century. Stansberry has released a new documentary naming the assets he believes are positioned to surge as a result.tc pixel
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About CRISPR Therapeutics

CRISPR Therapeutics (NASDAQ:CRSP) (NASDAQ: CRSP) is a biotechnology company focused on developing gene-editing medicines using CRISPR/Cas9 technology. The company’s programs are designed to modify disease-associated genes in human cells, with the goal of treating serious conditions across hematology, oncology, autoimmune disease and regenerative medicine.

Its most advanced product is Casgevy (exa-cel), an autologous cell therapy developed in collaboration with Vertex Pharmaceuticals. Casgevy uses CRISPR/Cas9 gene editing to modify a patient’s blood stem cells and is approved in several markets for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. The product was among the first medicines based on CRISPR gene-editing technology to receive regulatory approval.

Founded in 2013, CRISPR Therapeutics operates internationally, with corporate activities in Switzerland and the United States. In addition to its hemoglobinopathy program, the company is advancing investigational therapies in areas such as cancer, type 1 diabetes and immune-mediated diseases through both internal research and collaborations. Its scientific origins are associated with CRISPR pioneers Emmanuelle Charpentier and Rodger Novak, while Samarth Kulkarni has served as the company’s chief executive officer.

View CRISPR Therapeutics Profile