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RECRUITING Phase 1

Study of PF-07248144 in Advanced or Metastatic Solid Tumors

NCT04606446 · View on ClinicalTrials.gov ↗

Study Summary

This is an open-label, multi center study to evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of PF-07248144 and early signs of clinical efficacy of PF-07248144 as a single agent and in combination with other agents

Interventions

  • DRUG Letrozole
  • DRUG Fulvestrant
  • DRUG Palbociclib
  • DRUG PF-07220060
  • DRUG PF-07248144

Study Locations (20)

Tennessee

  • Tennessee Oncology PLLC — Franklin
  • Sarah Cannon Research Institute — Nashville
  • Tennessee Oncology PLLC — Nashville
  • The Sarah Cannon Research Institute / Tennessee Oncology, PLLC — Nashville

California

  • Cedars Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute — Los Angeles
  • Cedars-Sinai Medical Center; SOCCI Pharmacy — Los Angeles
  • UCSF Medical Center at Mission Bay — San Francisco

Connecticut

  • Smilow Cancer Hospital at Yale - New Haven — New Haven
  • Yale-New Haven Hospital- Yale Cancer Center — New Haven
  • Smilow Cancer Hospital Phase 1 Unit — New Haven

Kentucky

  • St. Elizabeth Healthcare — Edgewood
  • James Graham Brown Cancer Center — Louisville
  • University Medical Center, lnc.:DBA University of Louisville Hospital — Louisville

Texas

  • The University of Texas M. D. Anderson Cancer Center — Houston
  • U.T. MD Anderson Cancer Center — Houston
  • NEXT Oncology — San Antonio

Washington

  • Swedish Cancer Institute — Seattle
  • Swedish Medical Center — Seattle

Arizona

  • HonorHealth — Scottsdale

Florida

  • Holy Cross Hospital — Fort Lauderdale

Trial Details

FieldValue
Enrollment Target 320 participants
Start Date 2020-11-16
Est. Completion 2029-09-22
Phase Phase 1

Sponsor

Pfizer

769 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04606446

The ClinicalTrials.gov registry entry for NCT04606446 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 320 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Locally Advanced or Metastatic ER+ HER2- Breast Cancer appearing as the primary indexed condition, and to 5 interventions — of which Letrozole is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04606446 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Tennessee, California, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04606446 about?

NCT04606446 is a clinical study titled "Study of PF-07248144 in Advanced or Metastatic Solid Tumors". This is an open-label, multi center study to evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of PF-07248144 and early signs of clinical efficacy of PF-07248144 as a single agent and in combination with other agents

What is the current status of trial NCT04606446?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 320 participants. The study started on 2020-11-16. Estimated completion is 2029-09-22.

What conditions does trial NCT04606446 study?

This clinical trial studies the following conditions: Locally Advanced or Metastatic ER+ HER2- Breast Cancer, Locally Advanced or Metastatic Castration-resistant Prostate Cancer, Locally Advanced or Metastatic Non-small Cell Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04606446?

The interventions under investigation include: Letrozole (DRUG), Fulvestrant (DRUG), Palbociclib (DRUG), PF-07220060 (DRUG), PF-07248144 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04606446?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04606446 being conducted?

This trial has 20 study locations across Arizona, California, Connecticut, Florida, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial