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Pfizer Oncology
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The safety and efficacy of this agent(s), or use in this setting, has not been established or is subject to confirmation. For an agent(s) whose safety and efficacy has not been established or confirmed, future regulatory approval or commercial availability is not guaranteed.

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Important Notice: The information provided here relates to investigational therapies. The safety and efficacy of these investigational therapies has not been proven.

Poster

Exposure-Response Characterization of the Safety Profile for a Novel KAT6 Inhibitor, PF-07248144, For Use In Dose Optimization During a Phase 1 First-in-Patient Study

Liyanage M, Kowalski K, Williams JH, Huynh D, Li M, Masters JC

Prifetrastat (PF-07248144) | October 20, 2025 | ACoP 2025

C4551001 | NCT04606446

Poster

Model-Informed Recommended Phase 3 Dose for a novel KAT6 inhibitor, PF-07248144, Following Dose Optimization in 2L+ ER+/HER2- Metastatic Breast Cancer (mBC) population

Kowalski K, Liyanage M, Jermain B, Hahn E, Hee B, Pithavala Y, Li M, Masters J

Prifetrastat (PF-07248144) | September 15, 2025 | ACCP 2025

C4551002 | NCT07062965

Presentation

Dose optimization of PF-07248144, a first-in-class KAT6 inhibitor, in patients with ER+/HER2− metastatic breast cancer: results from phase 1 study to support the recommended phase 3 dose

LoRusso P, Mukohara T, Sommerhalder D, Yonemori K, Hamilton E, Layman RM, Kim SB, Im SA, Rugo HS, Yamashita T, Yan F, Hara F, Kim G, Wang S, Kent S, Liu L, Skoura A, Kowalski K, Li M, Park YH

Prifetrastat (PF-07248144) | May 30, 2025 | ASCO 2025

C4551001 | NCT04606446

Presentation

A phase 1 dose expansion study of a first-in-class KAT6 inhibitor — PF-07248144 in patients with advanced or metastatic ER+ HER2− breast cancer

Mukohara T, Park YH, Sommerhalder D, Yonemori K, Kim SB, Kim H, Iwata H, Yamashita T, Layman RM, Kim GM, Im SA, Lindeman GJ, Rugo HS, Liyanage M, Mishra NH, Maity AK, Bogg O, Meng Li M, LoRusso PM

Prifetrastat (PF-07248144) | June 1, 2024 | ASCO 2024

C4551001 | NCT04606446