LENZ Therapeutics, Inc. logo

LENZ Therapeutics, Inc. (GRPH)

Delisted
22 Mar 2024
NASDAQ (NMS) NASDAQ (NMS)
$
50. 00
+28.77
+135.5158%
$
185.19M Market Cap
- P/E Ratio
- Div Yield
20,800 Volume
-0.4 Eps
$ 21.23
Previous Close
Day Range
50 50
Year Range
2.01 50
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Summary

This company has been delisted from its primary exchange and is no longer publicly traded.
As a result, real-time price data, dividend updates, and corporate disclosures may no longer be available.

GRPH Chart

LENZ Therapeutics, Inc. (GRPH) FAQ

What does "Delisted" mean?

LENZ Therapeutics, Inc. has been removed from the exchange and is no longer publicly traded.

What was the last recorded dividend?

No dividend payments were recorded prior to delisting.

How long did the company pay dividends?

The company did not have a dividend payment history.

Were there any stock splits?

The last recorded stock split occurred on Mar 22, 2024 with a ratio of 1:7.

What was the last known trading price?

The stock last traded at $50.00 on Mar 22, 2024 before being delisted.

LENZ Therapeutics, Inc. Profile

- Industry
- Sector
Ms. Kimberlee Cobleigh Drapkin CPA CEO
NASDAQ (NMS) Exchange
38870X104 CUSIP
US Country
6 Employees
- Last Dividend
22 Mar 2024 Last Split
25 Jun 2021 IPO Date

Overview

Graphite Bio, Inc., originally founded as Integral Medicines, Inc. and later renamed in August 2020, embarked on a mission to advance the field of gene editing with its clinical-stage endeavors. The company's strategic aim was to tackle serious and life-threatening diseases, primarily within the United States. Marking a significant transition, Graphite Bio was acquired by LENZ Therapeutics, Inc. through a reverse merger on March 21, 2024. This pivotal move underscores the company's journey from its inception in 2017 in South San Francisco, California, towards becoming a cornerstone in gene therapy development for critical health conditions.

Products and Services

The therapeutic pipeline of Graphite Bio was meticulously designed to address a spectrum of genetic disorders, leveraging cutting-edge gene editing technology. Among its notable endeavors are:

  • GPH102: This innovative candidate targets beta-thalassemia, a hereditary blood disorder that significantly impairs the body's ability to produce hemoglobin. By correcting the genetic errors responsible for this condition, GPH102 aims to alleviate the severe anemia and other complications associated with beta-thalassemia.
  • GPH201: Focused on treating X-linked Severe Combined Immunodeficiency (XSCID), GPH201 represents a hope for patients with this deadly disease characterized by multiple mutations in a single gene. By precisely addressing these genetic anomalies, GPH201 seeks to restore normal immune function in affected individuals.
  • GPH301: Aimed at battling Gaucher disease, a genetic disorder leading to insufficient activity of the glucocerebrosidase enzyme, GPH301 is engineered to correct the underlying genetic defect. This approach has the potential to provide a transformative treatment for those suffering from Gaucher disease, mitigating the disease's systemic effects.

Contact Information

Address: 611 Gateway Boulevard, South San Francisco, CA, United States, 94080
Phone: 650 484 0886