Just reported
From Maze Therapeutics's results release of 2026年11月9日; its quarterly report has since been filed.
Actual
US$0.00
Guided
—
No guide given
Actual
-US$0.79
Guided
—
No guide given
Actual
-US$51.5M
Guided
—
No guide given
Set against the company's own guidance and the same quarter a year earlier, not analysts' estimates, which we do not hold. Adjusted figures are the company's own non-GAAP measures, as stated in the release.
The themes Maze Therapeutics is part of, the highest-graded companies in its industry, and the companies in its sector whose grade rose recently.
Graded A or B and worth $2B or more: A first, then the largest.
Rose to A or B on a filing in the last 90 days, worth $2B or more: largest first.
MZE829
An oral drug candidate designed to block APOL1, a protein linked to kidney damage in some people with inherited APOL1 gene variants. It is being tested in people with APOL1-related kidney disease.
MZE782
An oral drug candidate that blocks a transporter involved in moving amino acids through the gut and kidneys. It is being studied for PKU and is also being developed for chronic kidney disease.
MZE001
An oral drug candidate designed to reduce glycogen buildup in muscle in people with Pompe disease. Maze licensed it to Shionogi, which is developing it.
ATXN2 program
A gene therapy program designed to lower production of the ATXN2 gene product, which Maze studied as a possible approach to amyotrophic lateral sclerosis. Maze licensed the program to Neurocrine Biosciences.
UNC13A program
A drug research program based on the UNC13A gene and its link to amyotrophic lateral sclerosis and frontotemporal dementia. Maze licensed the program to Trace Neuroscience.
ANGPTL7 program
A research program for antibody drugs targeting ANGPTL7, a gene linked to eye pressure and glaucoma. The program is being developed by Broadwing, a company Maze formed with Alloy Therapeutics.
Maze uses human genetic and health data to find gene changes linked to disease and to identify drug targets. Its main drug candidates are designed for chronic kidney disease (CKD), including kidney disease linked to apolipoprotein L1 (APOL1), and phenylketonuria (PKU), an inherited disorder that causes harmful levels of an amino acid to build up. Maze also licenses some drug programs to other drug companies.
基于 Maze Therapeutics, Inc. 自己向美国证券交易委员会(SEC)提交的申报文件。数字如实呈报,每股历史已重述到今天的股数口径。 这是对一门生意的描述——不是投资建议,也不是买卖任何证券的推荐。
Maze is developing oral medicines for people with genetically defined kidney diseases and inherited metabolic disorders.
Not rated
价格下方的色带显示每个日期的评级,仅依据当时已公开的文件计算。