Just reported
From Maze Therapeutics's results release of 9 november 2026; 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 full earnings report →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 $2B or more: largest first.
MZE829
An oral drug candidate designed to block APOL1, a protein linked to kidney damage in some people with inherited APOL1 gene variants. It is being tested in people with APOL1-related kidney disease.
MZE782
An oral drug candidate that blocks a transporter involved in moving amino acids through the gut and kidneys. It is being studied for PKU and is also being developed for chronic kidney disease.
MZE001
An oral drug candidate designed to reduce glycogen buildup in muscle in people with Pompe disease. Maze licensed it to Shionogi, which is developing it.
ATXN2 program
A gene therapy program designed to lower production of the ATXN2 gene product, which Maze studied as a possible approach to amyotrophic lateral sclerosis. Maze licensed the program to Neurocrine Biosciences.
UNC13A program
A drug research program based on the UNC13A gene and its link to amyotrophic lateral sclerosis and frontotemporal dementia. Maze licensed the program to Trace Neuroscience.
ANGPTL7 program
A research program for antibody drugs targeting ANGPTL7, a gene linked to eye pressure and glaucoma. The program is being developed by Broadwing, a company Maze formed with Alloy Therapeutics.
Maze uses human genetic and health data to find gene changes linked to disease and to identify drug targets. Its main drug candidates are designed for chronic kidney disease (CKD), including kidney disease linked to apolipoprotein L1 (APOL1), and phenylketonuria (PKU), an inherited disorder that causes harmful levels of an amino acid to build up. Maze also licenses some drug programs to other drug companies.
Gebouwd uit de eigen deponeringen van Maze Therapeutics, Inc. bij de Amerikaanse toezichthouder Securities and Exchange Commission (SEC). De cijfers zijn zoals gerapporteerd, met de historie per aandeel herrekend naar de huidige aandelenbasis. Dit beschrijft een bedrijf — het is geen beleggingsadvies en geen aanbeveling om iets te kopen of te verkopen.
US$ 34,29-4,8%slot 13 nov
Cijfers tot en met 30 september 2026, uit de 10-Q ingediend op 9 november 2026
Maze is developing oral medicines for people with genetically defined kidney diseases and inherited metabolic disorders.
Not rated
De balk onder de koers toont het cijfer op elke datum, alleen gebaseerd op de stukken die toen al openbaar waren.