MARKET

CRSP

CRSP

Crispr Therapeut
NASDAQ
58.08
+0.51
+0.88%
Opening 15:46 07/26 EDT
OPEN
58.49
PREV CLOSE
57.57
HIGH
59.75
LOW
57.35
VOLUME
693.57K
TURNOVER
0
52 WEEK HIGH
91.10
52 WEEK LOW
37.55
MARKET CAP
4.93B
P/E (TTM)
-21.5140
1D
5D
1M
3M
1Y
5Y
1D
Actinium wins FDA nod to conduct clinical trial for radiotherapy
Healthcare Actinium wins FDA nod to conduct clinical trial for radiotherapy. Company's radiopharma candidate Iomab-ACT to be used as conditioning agent before bone marrow transplant in patients with sickle cell disease. The company will collaborate with Columbia University to conduct the study.
Seeking Alpha · 1d ago
CRISPR Therapeutics Stock Is Approaching Its 52-Week Low
TipRanks · 2d ago
Sangamo Therapeutics: A Bust Or Billion Dollar Valuation In The Remaking
Seeking Alpha · 3d ago
TD Cowen Reaffirms Their Sell Rating on Crispr Therapeutics AG (CRSP)
TipRanks · 3d ago
What's in Store for ADMA Biologics (ADMA) in Q2 Earnings?
NASDAQ · 4d ago
Weekly Report: what happened at CRSP last week (0715-0719)?
Weekly Report · 4d ago
CRISPR Therapeutics (CRSP) Moves 9.2% Higher: Will This Strength Last?
NASDAQ · 07/17 10:08
CRISPR Therapeutics (CRSP) Shares Cross Above 200 DMA
NASDAQ · 07/16 17:25
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About CRSP
CRISPR Therapeutics AG is a Switzerland-based gene editing company focused on the development of CRISPR/Cas9-based therapeutics. CRISPR/Cas9 stands for Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) and is a technology for gene editing, the process of precisely altering specific sequences of genomic DNA. The Company aims to apply this technology to disrupt, delete, correct and insert genes to treat genetically-defined diseases and to engineer advanced cellular therapies. The Company has acquired the rights to the intellectual property (IP) encompassing CRISPR/Cas9 and related technologies and is also involved in its own IP research and additional in-licensing efforts. The Company product development and partnership strategies are designed to exploit the full potential of the CRISPR/Cas9 platform while maximizing the probability of successfully developing their product candidates.

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