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PFEPfizerSigning up patients

Study to Test the Safety and Tolerability of PF-07220060 in Participants With Advance Solid Tumors

Liposarcoma · Prostate Cancer · Advanced Breast Cancer · NSCLC (Non-small Cell Lung Cancer) · Colorectal Cancer

0Calmworry score, out of 100

No strong warning signs right now. The score counts warning signs; it is not a prediction.

Why this score

No warning signs right now. That's why the score is 0.

Score over time

Stage
Phase 1/2
Patients
430 (planned)
Started
Sep 23, 2020
Main results expected
Oct 7, 2029
Fully finished
Oct 7, 2029
Results posted
not yet

What counts as success

The trial's main goal(s), called the “primary outcome.”

  • Number of participants with dose limiting toxicities in the Dose Escalation or De-escalation Portion

    Measured over: At the end of Cycle 1 (each cycle is 28 days)

  • Incidence of clinically significant AEs

    Measured over: Cycle 1 (each cycle is 28 days) through study completion, up to approximately 24 months

  • Incidence of clinically significant laboratory assessments

    Measured over: Cycle 1 (each cycle is 28 days) through study completion, up to approximately 24 months

  • Incidence of clinically significant abnormal vital and ECG parameters

    Measured over: Cycle 1 (each cycle is 28 days) through study completion, up to approximately 24 months

  • Maximal Plasma Concentration (Cmax) of PF-07220060 given with and without food

    Measured over: Cycle 1 (each cycle is 28 days)

  • Time to Maximum Plasma Concentration (Tmax) of PF-07220060 given with and without food

    Measured over: Cycle 1 (each cycle is 28 days)

  • Area Under the Plasma Concentration Versus Time Curve from Time Zero to the Last Sampling Time Point (AUClast) of PF-07220060 given with and without food

    Measured over: Cycle 1 (each cycle is 28 days)

  • Maximal Plasma Concentration (Cmax) of Midazolam with and without PF-07220060

    Measured over: Cycle 1 (each cycle is 28 days)

  • Time to Maximum Plasma Concentration (Tmax) of Midazolam with and without PF-07220060

    Measured over: Cycle 1 (each cycle is 28 days)

  • Area Under the Plasma Concentration Versus Time Curve from Time Zero to the Last Sampling Timepoint (AUClast) of Midazolam with and without PF-07220060

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Maximal Concentration (Cmax,ss) of PF-07220060

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Time to Maximum Plasma Concentration (Tmax,ss) of PF-07220060

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Area Under the Plasma Concentration Versus Time Curve Within One Dose Interval (AUCτ,ss) of PF-07220060

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Minimum Plasma Concentration (Cmin,ss) of PF-07220060

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Maximal Concentration (Cmax,ss) of Giredestrant

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Time to Maximum Plasma Concentration (Tmax,ss) of Giredestrant

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Area Under the Plasma Concentration Versus Time Curve Within One Dose Interval (AUCτ,ss) of Giredestrant

    Measured over: Cycle 1 (each cycle is 28 days)

  • Steady State Minimum Plasma Concentration (Cmin,ss) of Giredestrant

    Measured over: Cycle 1 (each cycle is 28 days)

Changes Tremor has spotted

  • Paperwork edit (contacts, locations, wording). Usually harmless.

    Spotted on Nov 6, 2026

Show details (technical version)

Score inputs

  • none

Raw record changes

  • 2026-11-06 15:29 UTC · paperwork · other
    old: null
    new: null
    details: {"sections":["referencesModule"]}

Trial ID NCT04557449 · record last updated 2026-10-28 · checked 2026-11-09 15:36 UTC

See the official record on ClinicalTrials.gov (NCT04557449) ↗