Oliver's mTOR Atlas Evidence Platform
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Justin G. Meyerowitz

Industry scientist on the team that developed RMC-5552, a bi-steric inhibitor selective for mTORC1

Revolution Medicines

Justin G. Meyerowitz Portrait: Doximity profile

Justin Meyerowitz is a scientist at Revolution Medicines in Redwood City, California, the affiliation PubMed gives on two of his mTORC1 papers. He co-authored the Journal of Medicinal Chemistry paper that described the discovery of RMC-5552, a bi-steric inhibitor designed to block mTORC1 while sparing mTORC2. The Atlas has no other sourced details of his career.

In the Atlas he is senior author of SCH2025, the first-in-human phase 1 trial of RMC-5552 in 57 people with advanced solid tumours. High blood sugar, a common problem with older mTOR inhibitors because they also hit mTORC2, occurred in only 4% of patients and was not dose-limiting. The trial had no comparison arm.

Milestones in the Atlas

A selection, not a full bibliography: only papers that meet the Atlas inclusion criteria.

YearEvidenceStudy
2025 H The Bi-steric, mTORC1-Selective Inhibitor, RMC-5552, in Advanced Solid Tumors: A Phase 1 Trial SCH2025 Senior author: phase 1 trial of the mTORC1-selective inhibitor RMC-5552 (n=57); treatment-related hyperglycaemia only 4% (humans, no comparator).

Co-authors in the Atlas 3

People with a profile here who share at least one study with Justin G. Meyerowitz.

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  • Alison M. Schram Medical oncologist at Memorial Sloan Kettering who runs first-in-human cancer drug trials, including the first trial of RMC-5552, an mTORC1-selective inhibitor
  • Howard A Burris Medical oncologist who led the Sarah Cannon Research Institute in Nashville as President and Chief Medical Officer, has run hundreds of early-phase cancer drug trials, including the first trial of the mTORC1-selective inhibitor RMC-5552, and was ASCO President in 2019–2020
  • Yu Chi Yang Scientist at Revolution Medicines who worked on the company's bi-steric mTORC1-selective inhibitors, from the breast cancer lab studies of RMC-6272 to the first trial of RMC-5552 in patients

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