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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.

IL-12 Mutein

Geo Regions

IL-12 Mutein

PF-07921585 is an investigational compound. Its safety and efficacy have not been established.

Overview + Rationale

RATIONALE FOR CANCER TARGET:

  • IL-12 is an established driver of T-cell differentiation and anti-tumor immunity, but previous attempts to use IL-12 as a target have demonstrated unacceptably high rates of toxicity1
  • IL-12 receptor agonism promotes anti-tumor immunity via direct enhancement of interferon-γ production and cytolytic capacity of CD8 T-cells and effects on CD4 T and NK cells2
  • PD-1 is highly expressed on CD4+ and CD8+ TILs compared to circulating  T-cell subsets2

 

OVERVIEW1

  • PF-07921585 is a first-in-class fusion of a human IL-12 mutein and a bivalent antihuman PD-1 full-length, Fc-null IgG1 designed to target human PD-1-expressing immune cell subsets while permitting simultaneous binding of anti-PD-1 antagonist antibodies
  • This antibody-cytokine fusion is designed to deliver IL-12 preferentially to PD-1 positive T cells in the tumor microenvironment, which may spare systemic effect, resulting in the potential for an improved therapeutic window

 

 

 

Mechanism of Action

In pre-clinical models, PF-07921585 targets a potency-reduced human IL-12 mutein to PD-1+ TILs with potential for anti-tumor immunity to drive anti-tumor immunity and could reduce IL-12 toxicities while also permitting simultaneous binding of PD-1 antagonists to enable combination with PDx therapy.

Stage of Development

Lung
Non-Small Cell Lung Cancer (NSCLC)
Phase 1 Monotherapy and Combination
Other
Advanced and Metastatic Solid Tumors
Phase 1 Monotherapy and Combination
This information is current as of February 4th 2025.